Abstract
Bone morphogenetic proteins (BMPs), members of the transforming growth factor-β (TGF-β) family, are multifunctional cytokines. BMPs have a broad range of functions, and abnormalities in BMP signaling pathways are involved in cancer progression. BMPs activate the proliferation of certain cancer cells. Malignant phenotypes of cancer cells, such as increased motility, invasiveness, and stemness, are enhanced by BMPs. Simultaneously, BMPs act on various cellular components and regulate angiogenesis in the tumor microenvironment. Thus, BMPs function as pro-tumorigenic factors in various types of cancer. However, similar to TGF-β, which shows both positive and negative effects on tumorigenesis, BMPs also act as tumor suppressors in other types of cancers. In this article, we review important findings published in the recent decade and summarize the pro-oncogenic functions of BMPs and their underlying mechanisms. The current status of BMP-targeted therapies for cancers is also discussed.
Introduction
Bone morphogenetic proteins (BMPs) were originally identified as bone- and cartilage-inducing factors in the bone matrix (Wozney et al., 1988; reviewed in; Katagiri & Watabe, 2016). Subsequent studies revealed that BMPs exert a wide range of biological effects. Since then, a variety of BMP roles have been shown in cancer progression. BMPs induce the proliferation of several types of cancer cells, suggesting that BMPs act as pro-tumorigenic factors. BMPs enhance malignant phenotypes of cancer cells, such as cell motility and invasiveness. BMPs also act on various cellular components in the tumor microenvironment, regulating angiogenesis and the immune landscape. In contrast, BMPs serve as tumor suppressors in certain types of cancers. These divergent roles of BMPs have been discussed in many other review articles, including our previous review articles (Ehata, et al., 2013; Davis et al., 2016). However, the precise mechanisms for the pro-oncogenic or tumor-suppressive functions of BMPs remain to be elucidated.
Bone Morphogenetic Protein Signaling Pathway
BMPs, which are members of the transforming growth factor-β (TGF-β) family, are multifunctional cytokines. More than a dozen BMPs have been identified in vertebrates (Figures 1A,B) (Miyazono et al., 2010; Morikawa et al., 2016). Several BMPs are also known as osteogenic proteins (OPs) or growth differentiation factors (GDFs). BMPs bind to two different groups of cognitive kinase receptors, namely type I and type II TGF-β family receptors, both of which are required for signal transduction. Unlike TGF-β, certain BMPs can bind to type I receptors in the absence of type II receptors. However, the binding affinities of BMPs to type I receptors are facilitated by the presence of type II receptors. Among the five different type II receptors in mammals, BMPs bind to BMP type II receptor (BMPR-II), activin type II receptor (ActR-II), and activin type IIB receptor (ActR-IIB). Among the seven type I receptors, BMPs bind to activin receptor-like kinase (ALK) 1, 2, 3, and 6 (Figures 1B,C).
FIGURE 1
Activation of BMP signaling pathways by various BMP ligands and type II and type I receptors. (A) Three-dimensional structure of human BMP-6 homodimer. This figure is created based on the PDB information deposited by Juo and Seeherman (https://www.rcsb.org/structure/6OMO). (B) Classification of BMPs based on their binding affinities to receptors. (C) BMPR-II, ActR-II, and ActR-IIB are type II receptors, while ALK1, ALK2, ALK3, and ALK6 are type I receptors for BMPs. The binding profiles of BMP-2/4 group, the BMP-5/6/7/8 group, the GDF-5/6/7 group, and the BMP-9/10 group to type I receptors are shown. *BMPs of BMP-2/4 group preferentially bind to ALK3 and ALK6, while those of OP-1 group mainly bind to ALK2 and ALK6. However, BMP-2/4 may transduce signals through ALK2, while OP-1 group ligands may transduce signals through ALK3 under certain conditions. Type II and type I receptors form a heteromeric complex and transduce intracellular signals by phosphorylating Smad1/5, as well as through non-Smad signaling pathways. The phosphorylated Smads form complexes with Smad4 and associate with various transcription factors and transcriptional coregulators in the nucleus, thereby regulating transcription of the target genes, including ID1.
BMPs can be classified into four subgroups according to their structural similarities and ability to bind to type I receptors (Miyazono et al., 2010; Sanchez-Duffhues et al., 2020). The BMP-2/4 group preferentially binds to ALK3 and ALK6, whereas the BMP-5/6/7/8 group mainly binds to ALK2 and ALK6. The GDF-5/6/7 (also known as BMP-12/13/14) group binds to ALK6, but does not bind to other type I receptors. The BMP-9/10 group binds to ALK1 and binds weakly to ALK2. BMP signaling is modified by membrane proteins, as well as by diverse secreted proteins (Brazil et al., 2015; Correns et al., 2021). A co-receptor, endoglin (also known as CD105) upregulates BMP-9/10-ALK1 signaling in endothelial cells and downregulates TGF-β-ALK5 signaling (Dallas et al., 2008). BMP and activin membrane bound inhibitor (BAMBI) acts as a pseudoreceptor and negatively regulates BMP signaling. Structurally diverse secreted proteins, such as noggin, chordin, and gremlin1, bind directly to BMPs and regulate their availability as antagonists (Chang et al., 2016).
Upon binding to type I and type II receptors, BMPs form heterotetrameric receptor complexes (Miyazono et al., 2010). Type II receptor serine/threonine kinases are constitutively active, and they activate type I receptor kinases through phosphorylation of the Gly-Ser-rich (GS) domain of type I receptors. Type I receptors activate receptor-regulated Smads (R-Smads: Smad1 and Smad5). Although Smad8 (also known as Smad9) is structurally similar to Smad1 and Smad5, its function has not been fully elucidated. Recent findings have suggested that Smad8 acts as an antagonist of Smad1/5 (Tsukamoto et al., 2014). Some mutations affect residues in the GS domain or the ATP-binding pocket of the kinase domain of ALK2, leading to increased phosphorylation of R-Smads (Wu et al., 2014; Sanchez-Duffhues et al., 2020). Phosphorylated R-Smads induce heteromeric assembly with the common partner Smad (Co-Smad; Smad4). R-Smad/Co-Smad complexes bind to various transcription factors and transcriptional co-activators [p300, cAMP response element-binding protein-binding protein (CBP), and general control non-depressible 5 (GCN5)] or co-repressors (c-Ski and SnoN) in the nucleus, leading to regulation of the transcription of target genes, including inhibitor of DNA binding (ID)1. Inhibitory Smads (I-Smads; Smad6, and Smad7) repress TGF-β family signaling, mainly through interaction with type I receptors (Miyazawa & Miyazono, 2017). While both TGF-β signaling and BMP signaling are inhibited by Smad7, Smad6 preferentially inhibits BMP signaling through ALK3 and ALK6 (Goto et al., 2007). In addition to these Smad-dependent signaling pathways, BMPs activate non-Smad signaling pathways, including the extracellular signal-regulated kinase (Erk), c-Jun N-terminal kinase (Jnk), p38 mitogen-activated protein (MAP) kinase, phosphoinositide 3 (PI3) kinase-Akt, and small GTPase pathways. Non-Smad signaling pathways cooperate with Smad signaling pathways to regulate various cellular responses.
Altered Expression of Bone Morphogenetic Proteins and Their Signaling Components in Cancers
Altered expression of BMPs or related signaling components has been observed in many cancers. In addition to conventional histopathological analyses using clinical specimens, analyses of public databases have indicated the clinical significance of BMPs in cancer progression. Here, we introduce recent findings for each type of cancer.
Hepatocellular Carcinoma
Numerous reports have suggested that BMP signaling is activated in hepatocellular carcinoma (HCC) tissues. The expression levels of BMP-2/4 and ALK3 were upregulated in tumor tissues. Many of these are correlated with various clinical or biological parameters, such as unfavorable prognosis, tumor grade, TNM stage, vascular invasion, and the expression of the stem cell marker CD133 (Guo D et al., 2012; Zhang et al., 2012; Ma et al., 2017; Feng et al., 2019; Li et al., 2020; Guo et al., 2021). Increased BMP-9 expression is also observed in HCCs and significantly associated with poor outcomes and the T stage of HCC (Herrera et al., 2013; Li et al., 2013; Chen et al., 2021). Of note, high levels of BMP-9 were detected, especially at the tumor borders, in samples from an HCC mouse model (Li et al., 2013). Although conflicting data have also been reported (Wang et al., 2018), the pro-oncogenic function of BMP signaling in HCC has been supported by many reports.
Colorectal Cancer
It is well known that germline mutations in MADH4 or BMPR1A (encoding Smad4 or ALK3, respectively) are present in a large number of patients with juvenile polyposis syndrome (Ehata et al., 2013). Phosphorylation of Smad1/5 has been reported to be absent in most colorectal cancers (CRCs). A recent study estimated that methylation of BMP2 occurs in 60.2% of sporadic CRCs (Miura et al., 2020). Based on these findings, many reports have indicated that BMPs act as tumor suppressors in CRC. On the contrary, BMP signaling also acts as a pro-tumorigenic factor by promoting tumor invasion, epithelial-mesenchymal transition (EMT), and tumor proliferation (Davis et al., 2016). Fan et al. revealed that BMP-9 expression gradually increased during the transition from normal mucosa to adenoma and subsequent adenocarcinoma in the colon (Fan et al., 2020). Our analysis showed that BMP-4 was highly expressed in CRC tissues compared to normal tissues, and that BMP-4 is involved in CRC progression as an autocrine factor (Yokoyama et al., 2017). One possible explanation for the different roles of BMPs in CRC might be the BMP-induced non-Smad signaling pathway. Based on the expression of the BMP receptor and Smad4, Voorneveld. et al. subdivided CRC cases and found that the expression of normal BMP receptors in Smad4-negative tumors was associated with poor prognosis, suggesting that Smad4-independent BMP signaling may accelerate the progression of CRC (Voorneveld et al., 2014). They also reported that patients with a combination of high BMP-2 expression in the stroma and loss of Smad4 in tumors showed a significantly poorer overall survival (Ouahoud et al., 2020).
Lung Cancer
In non-small cell lung cancers, elevated serum BMP-2 levels are observed in many patients, and they serve as a marker for effective treatment (Choi et al., 2012; Fei et al., 2013). In contrast, Liu et al. revealed that in small cell lung cancers, BMP-7 expression was not detected in cancer tissues, and that BMP-7-positive tumors were correlated to the absence of bone metastasis (Liu et al., 2012).
Breast Cancer
There are still conflicting data regarding the role of BMPs in the progression of breast cancer. The activation of Smad-dependent BMP signaling has been observed in primary and metastatic bone tumors in breast cancer (Katsuno et al., 2008; Owens et al., 2015). BMP-2/5/6/7 are observed in breast cancers and are correlated with the expression of the stem cell marker CD44 (Owens et al., 2015; Huang et al., 2017). The expression of BMPR1A (encoding ALK3) is correlated with poor relapse-free survival (Pickup et al., 2015). However, an inverse correlation was observed. BMP-5 expression is decreased in invasive breast cancer, and is associated with cancer recurrence (Romagnoli et al., 2012). The expression of BMP-9 is significantly decreased in the breast cancer tissues, compared with paracancerous tissues (Li et al., 2018). The expression of BMP antagonists, such as noggin or follistatin, is correlated to bone metastasis, but not to metastasis to other organs (Tarragona et al., 2012; Mock et al., 2015).
Renal Cell Carcinoma
Although BMP-9 expression is found over 80% of RCC (Wang et al., 2016), recent studies mainly support the tumor-suppressive role of BMPs in renal cell carcinoma (RCC). BMP-2 is downregulated by the promoter CpG methylation of BMP2 in RCC cells. The resultant loss of BMP-2 is correlated to poor prognosis in RCC (Mitsui et al., 2015). Consistent with these findings, we observed increased expression of the transcriptional co-repressor c-Ski in cancer cells in RCC tissues (Taguchi et al., 2019). However, it should be mentioned that c-Ski may accelerate cancer progression mainly through the suppression of TGF-β-dependent Smad signaling, and not through the suppression of BMP-dependent Smad signaling in an experimental setting. Our latest data also indicated that endoglin expression was heterogeneously upregulated in highly malignant derivatives obtained after serial transplantation of human RCC cells (Momoi et al., 2021).
Ovarian Cancer
The expressions of BMPs and their signaling components, BMP-2/7, ALK2/3, BMPR-II, and phosphorylated Smad5, are elevated in ovarian cancers (Hover et al., 2015; Peng et al., 2016; Guan et al., 2019; Fukuda et al., 2020). These findings consistently suggest pro-oncogenic roles of BMPs. Moreover, Fukuda et al. observed high BMP-2 expression after chemotherapy for ovarian cancer (Fukuda et al., 2020). The role of anti-Müllerian hormone (AMH), a member of the TGF-β family, has also been investigated in ovarian cancers. AMH activates the Smad1/5-mediated signaling pathway through the binding to AMH type II receptors (AMHRII) and type I receptors (ALK2/3/6). AMH is produced by granulosa cells in females, and it acts as a key factor in sexual differentiation. Interestingly, AMH has been shown to inhibit the proliferation of ovarian granulosa cell tumor cells (Anttonen et al., 2011) and epithelial ovarian cancer cells (Zhang et al., 2018). Further analyses are needed to elucidate the role of BMP signaling in ovarian cancer.
Endometrial Cancer
High expression of BMP2 and BMP7 mRNA is associated with poorer survival in patients with endometrial cancer, albeit not significantly for BMP2 (Fukuda et al., 2021). In addition, mutations in ACVR1, the gene encoding ALK2, are more frequently observed in endometrial cancer (>6%) than in most other cancers. Mutations in ACVR1 were originally found in patients with fibrodysplasia ossificans progressiva (FOP) (Shore et al., 2006), and have also been found in pediatric brain tumors (see below). The mutant ALK2 in the GS domain (R206H) shows hyperactivation of the kinase domain, and it acquires the ability to bind activins and BMPs (Hatsell et al., 2015). Concerning the expression of BMP-10, a controversial implication has also been reported in endometrial cancer (Hu et al., 2021).
Prostate Cancer
In prostate cancer, decreased BMP-2 expression in cancer tissue is correlated to recurrence and the Gleason score, which represents histological patterns and prognosis (Tae et al., 2018). We have also reported that BMP-7 inhibits the proliferation of prostate cancer cells in cell culture and a xenograft model (Miyazaki et al., 2004). However, BMP-7 expression in metastatic prostate cancer tissues is associated with shorter patient survival, suggesting a context-dependent contribution of BMPs in prostate cancer (Liu et al., 2015).
Squamous Cell Carcinoma in the Esophagus, Head, and Neck
Two independent groups revealed that high BMP-7 was observed in primary esophageal cancer tissues, with a correlation to prognosis and metastasis-related parameters (Megumi et al., 2012; Xu et al., 2013). Interestingly, the level of phosphorylated Smad1/5 is elevated in the tumor tissues of patients with cetuximab-resistant oral squamous cell carcinoma with poor prognosis (Yin et al., 2018).
Nasopharyngeal Carcinoma
High BMP2 expression is significantly associated with clinical stage, distant metastasis, and shorter survival in patients with nasopharyngeal carcinoma (Wang et al., 2017).
Glioma
BMPs suppress the tumorigenic function of human glioma-initiating cells by inducing cell differentiation, cell cycle arrest, and apoptosis (see below). Accordingly, several reports have shown that BMP-4 is expressed in low-grade gliomas, and that it serves as a favorable prognostic marker in gliomas (Bao et al., 2013; Nayak et al., 2020). BMP-4 is overexpressed in gliomas harboring IDH1 mutations, which are a hallmark of better prognosis (Zhou et al., 2020).
In contrast, in diffuse intrinsic pontine glioma (DIPG), a glial tumor in the brainstem with highly infiltrative properties in children, mutations in ACVR1 may exhibit pro-oncogenic functions. Four independent research groups reported that ACVR1 mutations were found in approximately 20–30% of DIPG (Buczkowicz et al., 2014; Fontebasso et al., 2014; Taylor et al., 2014; Wu et al., 2014). Notably, many somatic ACVR1 mutations in DIPG are identical to germline mutations found in FOP. However, given that FOP is not accompanied by a tumor predisposition, other oncogenic mechanism(s) are required for the pathogenesis of DIPG. The increased activation of ACVR1 may contribute to the pathogenesis of DIPG in the presence of several histone modifications. Co-expression of ACVR1 G328 and histone H3.3K27M additively increased the expression of ID1 and ID2 (Buczkowicz et al., 2014). Evolutionary analysis showed specific associations between H3K27M and mutations in TP53, PPM1D, ACVR1, and PIK3R1 (Nikbakht et al., 2016). Hoeman et al. recently demonstrated that ACVR1 R206H or G328V with H3.1K27M activates signal transducer and activator of transcription 3 (STAT3) signaling (Hoeman et al., 2019). Inhibition of BMP signaling may suppress the progression of ACVR1 mutation-positive DIPG (Carvalho et al., 2019). However, how BMP signaling affects the progression of ACVR1 mutation-negative DIPG cells remains unknown. It should also be noted that mutations in the ACVR1 gene are observed in other types of cancers, including endometrial cancer, although the frequencies of the ACVR1 mutations are lower than those in DIPG (Fukuda et al., 2021).
Effect of Bone Morphogenetic Proteins on the Proliferation and Survival of Cancer Cells
BMPs promote the progression of many types of cancers through the activation of proliferation and survival of cancer cells (Ehata et al., 2013). The detailed mechanisms of these pro-oncogenic roles of BMPs have recently been uncovered, especially in HCC. BMP-4 upregulates the expression of cyclin-dependent kinase (CDK) 1 and cyclin B1 in HCC cells and accelerates cell cycle progression by activating Erk MAP kinase (Chiu et al., 2012). Ma et al. reported that exogenous BMP-4 increases the expression of cyclin A and CDK2 and promotes the G1-S phase transition in several HCC cells. The BMP-4-mediated cell proliferation was attenuated by silencing ID2 (Ma et al., 2017). The human HCC cell line HepG2 produces BMP-9 in an autocrine fashion, which triggers cell cycle progression and abolishes apoptosis induced by serum starvation. Notably, BMP-9 promotes the growth of HCC cells, but not of immortalized human hepatocytes, suggesting that other oncogenic signaling pathways may modulate the effect of BMP-9 (Herrera et al., 2013). BMP-4 has also been shown to promote the proliferation of HCC cells via autophagy activation through Jnk1/Bcl-2 signaling (Deng et al., 2018). In addition to HCC, the pro-survival effect of BMP signaling is indicated in other cancers. We have revealed that aberrant activation of the Wnt/β-catenin pathway induces BMP4 mRNA expression, activating endogenous BMP signaling in CRC cells (Figure 2). This endogenous signaling enhances the phosphorylation of Erk MAP kinase through the downregulation of dual-specificity phosphatase 5 (DUSP5), thereby promoting the survival of CRC cells (Yokoyama et al., 2017). Stress-induced phosphoprotein 1 (STIP1) is secreted by ovarian cancer cells. The binding of STIP1 to ALK2 activates the Smad signaling pathway, leading to the transcriptional activation of ID3, promoting cell proliferation (Tsai et al., 2012). Most of ACVR1 mutations in DIPG cause constitutive activation of ALK2, which increases the expression of the downstream targets ID1, ID2, and SNAI1 (encoding Snail), and also increases cell proliferation (Buczkowicz et al., 2014; Fontebasso et al., 2014). Treatment of tumor cells with a small-molecule ALK2 inhibitor, LDN-193189, attenuated their viability (Taylor et al., 2014).
FIGURE 2
Role of autocrine BMP-4 signaling in CRC. Aberrant activation of the Wnt/β-catenin pathway induces expression of BMP4 mRNA, activating endogenous BMP signaling. This endogenous signaling promotes phosphorylation of Erk MAP kinase via DUSP5 suppression, which results in survival of CRC cells. Modified from Yokoyama et al. (2017).
In contrast, BMPs have been shown to negatively regulate cell cycle progression in other types of cancer cells, including gastric and prostate cancer cells (Ehata et al., 2013). We previously found that BMP-4 induces G1 arrest in diffuse-type gastric carcinoma cells via induction of p21 through the Smad pathway, inhibiting cell proliferation (Shirai et al., 2011). Similarly, BMP-2 inhibits esophageal cancer cell growth by inducing p21 through the Smad pathway and activating the Hippo signaling pathway (Kim et al., 2016). BMP-7 also inhibits prostate cancer cell proliferation by inducing p21 and suppressing CDK2 activity (Miyazaki et al., 2004). BMP-10 suppresses the proliferation of HCC cells by inhibiting the signal transducer and activator of transcription 3 (STAT3) signaling. Mechanistically, cytoplasmic BMP-10 interacts with both protein tyrosine phosphatase sigma (PTPRS) and STAT3, thus facilitating the dephosphorylation of STAT3 by PTPRS (Yuan et al., 2019). Olsen et al. reported that BMP-9 induces apoptosis in multiple myeloma cells through the ALK2-mediated signaling pathway (Olsen et al., 2014). As different types of cancers cannot account for the diverse effects of BMPs, they are thought to regulate the proliferation or survival of each cancer cell in a context-dependent manner.
Effect of Bone Morphogenetic Proteins on Cancer Stem Cells
Cancer stem cells (CSCs) or cancer-initiating cells may be responsible for cancer recurrence. As BMPs act as differentiation factors in several organs, the activity of CSCs is diminished by BMPs. BMPs induce differentiation of glioma-initiating cells, leading to cell cycle arrest or apoptosis (Piccirillo et al., 2006; Lee et al., 2008). Various mechanisms have been determined for the BMP-mediated differentiation of glioma-initiating cells. BMPs induce the EMT-associated transcription factor Snail via Smad-dependent pathways, which results in the deletion of tumorigenic potential (Savary et al., 2013). As a mechanism, Snail transcriptionally represses TGFB1 through interaction with Smads, thereby regulating astrocytic differentiation (Caja et al., 2018). Our research group has also shown that distal-less homeobox 2 (DLX2), an essential transcription factor induced by BMPs, is important for neural differentiation and apoptosis of glioma-initiating cells (Raja et al., 2017). In addition to these transcription factors, BMPs affect glioma-initiating cells via epigenetic mechanisms. We found that the expression of paired related homeobox 1 (PRRX1) is induced by BMPs in glioma-initiating cells. The longer isoform of PRRX1, pmx-1b, interacts with DNA methyltransferase 3A (DNMT3A) and induces promoter methylation of the PROM1 gene encoding CD133, thereby attenuating stem cell-like properties (Tanabe et al., 2022) (Figure 3). We have also reported that the tyrosine kinase Eph receptor A6 (EPHA6) promotes apoptosis in BMP-2-sensitive glioma-initiating cells (Raja et al., 2019). BMPs thus play tumor-suppressive roles in the progression of glioma, acting on glioma-initiating cells. However, some glioma cells acquire resistance to the action of BMP-Smad signaling pathways, and several extracellular proteins are associated with the sensitivity of some glioma cells to BMPs. Increased expression of the extracellular antagonists gremlin1 or follistatin-like 1 promotes the maintenance of glioma-initiating cells through the attenuation of BMP signaling (Yan et al., 2014; Jin et al., 2017).
FIGURE 3
BMPs induce differentiation and apoptosis of glioma-initiating cells. BMPs regulate expression of various target genes in glioma-initiating cells. In this figure, the roles of PRRX1 (Tanabe et al., 2022) and gremlin1 (Yan et al., 2014) are shown. Of the two splice isoforms of PRRX1, only pmx-1b induces differentiation of glioma-initiating cells. Through interaction with DNMT3A, pmx-1b induces the methylation of the PROM1 gene promoter and suppressed the CD133+ glioma-initiating cell population. BMPs induce the expression of gremlin1, an antagonist of BMP, which is involved in the maintenance of pro-tumorigenic functions and stem cell properties of glioma-initiating cells. Modified from Tanabe et al. (2022).
Likewise, the effect of BMPs on the differentiation of CSCs has been investigated in cancers other than glioma. Although TGF-β-induced EMT may render breast cancer cells with stem cell properties, BMPs, particularly heterodimeric BMP-2/7, antagonize TGF-β-induced EMT and reduce the aldehyde dehydrogenase (ALDH)h CD44h CD24l− CSC population (Buijs et al., 2012). In normal mammary epithelial cells, BMP-4 acts as a pro-differentiation factor and promotes acinar formation. However, in triple-negative breast cancer (TNBC) cells, TGF-β inhibits the expression of BMP-4 through the Smad pathway and cyclin D1. Thus, TGF-β enhances tumor formation and increases the highly tumorigenic CD44high CD24low CSC population (Yan et al., 2021). Whissel et al. found that BMP4 transcription is regulated by GATA-binding protein 6 (GATA6), which is related to the self-renewal of adenoma stem cells in the colon (Whissell et al., 2014). In RCC cell lines, BMP-2 downregulates the expression of stem cell markers in ALDH+ cells and potently inhibits their growth (Wang et al., 2015). CSC-like cells in head and neck cancer display decreased levels of phosphorylated Smad1/5 and BMP target gene ID1, whereas Smurf1, a negative regulator of BMP signaling, is highly expressed compared to that in non-CSC populations. When BMP signaling pathways are reactivated by Smurf1 knockdown in CSC-like cells, adipogenic differentiation and loss of tumorigenic capacity are observed (Khammanivong et al., 2014). BMP-2 is thought to act as a potent inducer of tumor cell transdifferentiation in osteosarcoma (Geng et al., 2014).
These observations indicate that BMPs promote the differentiation of CSCs and attenuate the tumor-forming capability of several cancer cells. Thus, BMP administration is thought to be suitable for these cancers (Reguera-Nuñez et al., 2014; Nayak et al., 2020). For example, exogenous BMP-4 induces the differentiation of CSCs within HCC through the activation of the Erk1/2 MAP kinase signaling pathway, inhibiting the self-renewal and tumorigenic capacities of CD133+ CSCs. Simultaneously, the expression of one of the ABC transporters, ATP-binding cassette subfamily G member 2 (ABCG2), is decreased in hepatic cancer stem cells after BMP-4 treatment, which enhances sensitivity to chemotherapeutic agents (Zhang et al., 2012). González-Gómez et al. employed BMP-7-loaded microspheres in a xenograft model and demonstrated that controlled release of BMP-7 potently inhibited the growth of glioblastoma and reduced CSC markers, including CD133, Olig2, and glial fibrillary acidic protein (GFAP)δ (González-Gómez et al., 2015).
However, BMPs are also important for the maintenance of CSCs in HCC. Zhang et al. revealed that high-dose exogenous BMP-4 promotes the differentiation of CD133+ CSCs in HCC, whereas low-dose exogenous BMP-4 upregulates CD133 expression, suggesting a concentration-dependent effect of BMPs on CSC maintenance (Zhang et al., 2012). Silencing of BMP-2 in HCC suppresses Erk MAP kinase and inhibits sphere formation and the expression of stemness-related and EMT markers in CSCs from HCC cell lines (Guo et al., 2021). BMP-9 promotes CSC properties in epithelial cell adhesion molecule (EpCAM)-positive HCC subtypes by enhancing ID1 expression (Chen et al., 2021).
Effect of Bone Morphogenetic Proteins on Cancer Cell Migration, Invasion, and Metastasis
Similar to TGF-β, BMPs enhance the migration and invasion of several types of cancer cells, thereby potentiating their metastatic ability. This pro-metastatic function of BMPs has been supported by numerous recent studies (Guo X et al., 2012; Maegdefrau & Bosserhoff, 2012; Xu et al., 2013; Leinhäuser et al., 2015; Liu et al., 2015; Guan et al., 2019; Huang et al., 2020). The BMP-Smad pathway plays a critical role in the induction of EMT in many cancer cells. For example, BMP-4 induces the expression of the EMT-associated transcription factors SNAI1 and SNAI2, which encode Snail and Slug, respectively, in a Smad4-dependent manner in ovarian and pancreatic cancer cells. This regulatory mechanism is critically dependent on matrix rigidity and Yes-associated protein 1 (YAP1) (Serrao et al., 2018). BMP-4 enhances EMT and stem cell properties via the Smad-dependent pathway in both mammary epithelial and breast cancer cells, which is accompanied by the activation of Notch signaling (Choi et al., 2019). In HCC cell lines, autocrine BMP-9 signaling induces Snail expression via the ALK1- and ALK2-Smad1 pathways (Li et al., 2013).
Non-Smad pathways, including PI3 kinase-Akt, mTOR, and Rock, are involved in BMP-mediated EMT. BMP-2 induces EMT and stemness of breast cancer cells through the Rb and CD44 signaling pathways, which act not only via Smad-dependent pathways but also via the PI3 kinase-Akt signaling pathway (Huang et al., 2017). The mTORC1 inhibitor rapamycin blocks BMP-2-induced EMT in nasopharyngeal carcinoma cells (Wang et al., 2017). In CRC, Smad4-independent BMP signaling induces EMT and invasion via the Rock pathway (Voorneveld et al., 2014). In chondrosarcoma cells, BMP signaling regulates the expression of matrix metalloproteinases (MMPs) and promotes invasiveness via non-Smad signaling pathways, including p38 MAP kinase and Akt pathways (Chen et al., 2014; Yahiro et al., 2019).
Despite these findings, exogenous BMP-2 does not affect the metastatic phenotype of osteosarcoma cells (Gill et al., 2017). Moreover, the suppressive effects of BMPs on metastasis have been documented in breast cancer and osteosarcoma (Ren et al., 2014a; Ren et al., 2014b; Xiong et al., 2018). Overexpression of some BMP antagonists, such as gremlin1 or noggin, promotes metastasis of breast cancer cells (Tarragona et al., 2012; Sung et al., 2020). Although the reason for these conflicting effects remains unclear, the experimental methods employed in each report might have affected the function of BMPs.
Effect of Bone Morphogenetic Proteins on Tumor Angiogenesis
ALK1 is predominantly expressed in proliferating vascular endothelial cells. As BMP-9/10 have been identified as ligands for ALK1, the role of BMP-9/10-ALK1 signaling in vascular angiogenesis has been well established (see Figure 1) (Ehata et al., 2013). The BMP-9/10-ALK-1 signaling pathway activates the proliferation of endothelial cells under certain conditions, and plays an important role in the maintenance of vascular homeostasis. We previously showed that BMP-9 induces tumor angiogenesis in a mouse xenograft model of human pancreatic cancer (Suzuki et al., 2010). However, the effect of BMP-9/10-ALK1 signaling on lymphatic endothelial cells may differ from that on vascular endothelial cells. Yoshimatsu et al. revealed that BMP-9 directly downregulates prospero homeobox 1 (Prox1) expression via ALK1 in human dermal lymphatic endothelial cells (HDLECs) and reduces their proliferation. BMP-9 was shown to inhibit tumor lymphangiogenesis in a mouse breast cancer allograft model (Yoshimatsu et al., 2013).
In contrast to BMP-9/10-ALK1 signaling, the role of ALK2/3/6-mediated BMP signaling in angiogenesis remains controversial. Elevated expression of BMP-2 is found in HCC and is positively correlated to angiogenesis in tumor tissues. A loss-of-function assay using shRNAs revealed that BMP-2 secreted from HCC cells activates the p38 MAP kinase signaling pathway in endothelial cells, thus enhancing the proliferation, migration, and angiogenic abilities of endothelial cells (Feng et al., 2019). BMP-7 exhibits a pro-angiogenic effect through the expression of repulsive guidance molecule family member B (RGMb), a co-receptor for BMPs, in endothelial cells (Sanders et al., 2014). Taken together, the impairment of tumor angiogenesis may be achieved by blocking BMP signaling pathways other than BMP-9/10-ALK1 (Jia et al., 2016). However, under certain conditions, the direct administration of BMPs to tumor-bearing mice exerts an anti-angiogenic effect. Intraperitoneal treatment with BMP-4 suppressed tumor angiogenesis and reduced tumor formation in xenograft and allograft models of some cancer cells. As its mechanism, BMP-4 reduces vascular endothelial growth factor (VEGF) expression in vivo in a thrombospondin 1 (TSP1)-dependent manner (Tsuchida et al., 2014). BMP-7v, a modified BMP-7, is capable of reducing the number of microvessels in CSC-based avatars, resulting in the sensitization of CRC cells to chemotherapeutic reagents (Veschi et al., 2020).
Effect of Bone Morphogenetic Proteins on Other Cellular Components in the Tumor Microenvironment
BMPs mediate the interactions between cancer cells and various cellular components in the tumor microenvironment. BMP-4 expression is upregulated in cancer-associated fibroblasts (CAFs) in HCC tissues compared to non-cancerous liver fibroblasts. BMP-4 overexpression in normal fibroblasts activates these cells to a CAF-like phenotype. Simultaneously, BMP-4 enhances the production of interleukin (IL)-6, IL-8, and chemokine (C-C motif) ligand (CCL)2 and promotes cancer cell invasion (Mano et al., 2019). BMP-2 is upregulated in fibroblasts upon stimulation with conditioned medium from Smad4-deficient CRC cells, which in turn increases the liver metastasis of Smad4-deficient CRC cells, but not that of Smad4-proficient CRC cells. BMP-2 expression in fibroblasts appears to be regulated by tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) derived from Smad4-deficient CRC cells. Thus, a reciprocal loop in which TRAIL from Smad4-deficient CRC cells induces BMP-2 in fibroblasts plays a critical role in cancer progression (Ouahoud et al., 2020). BMPs and hedgehogs mediate the interactions between cancer cells and the tumor microenvironment. We previously reported that BMP-4 induces the production of sonic hedgehog in prostate cancer cells, thereby enhancing osteoblastic differentiation of stromal cells and may account for osteoblastic metastasis of prostate cancer (Nishimori et al., 2012). Hedgehogs secreted from ovarian tumor cells induce BMP-4 expression in carcinoma-associated mesenchymal stem cells. BMP-4 reciprocally increases hedgehog expression in ovarian tumor cells, indicating a positive feedback loop. The interruption of this loop with a hedgehog pathway inhibitor or BMP-4-blocking antibody prevents the enrichment of CSCs and reverses chemotherapy resistance (Coffman et al., 2016).
BMPs suppress anti-tumor immunity (reviewed in Sconocchia & Sconocchia, 2021). Recent studies revealed that BMP signaling is shown to be involved in the activation of macrophages or dendritic cells during cancer progression. Bladder cancer cells produce BMP-4, which enhances the macrophage polarization toward anti-inflammatory M2 phenotype (Martinez et al., 2017). BMP-4 derived from acute lymphoblastic leukemia cells promotes the generation of dendritic cells with immunosuppressive features and polarizes macrophages towards a less pro-inflammatory phenotype (Valencia et al., 2019). Ihle et al. utilized a LysMCre-mediated myeloid-specific Bmpr1a conditional knockout mouse model along with a syngeneic prostate cancer model and demonstrated the pro-tumorigenic role of ALK3 in myeloid cells. They also confirmed that macrophage polarization is altered by ALK3 inhibition in this setting (Ihle et al., 2020). BMP-7 is upregulated in tumors in a mouse model that does not respond to treatment with immune checkpoint inhibitors (Cortez et al., 2020). Mechanistically, tumor cell-derived BMP-7 downregulates MAP kinase (MAPK) 14, which regulates some cytokines and chemokines, including IL1A, IL1B, TNF, and CCL5 via Smad1 activation in macrophages.
The role of BMPs on the lymphocyte functions has recently been investigated. Kuczma et al. extracted Bmpr1a as a gene that regulate the immune suppressive function of regulatory T cells (Treg) (Kuczma et al., 2014). Inactivation of Bmpr1a in T cells resulted in impaired generation of Treg, leading to the reduced tumor growth in mice bearing B16 melanoma cells. BMP-7 decreases CD4+ T-cell activation by downregulating interferon γ and IL-2 expression via Smad/MAPK14 signaling, resulting in resistance to immunotherapy (Cortez et al., 2020). These findings support the idea that inhibition of BMP signaling may be beneficial for cancer treatment.
However, other reports have shown that BMPs suppress the function of tumor-promoting immune cells (Sconocchia & Sconocchia, 2021). BMP-4 reduces the secretion of granulocyte colony-stimulating factor (G-CSF) from mammary tumors, which is likely a critical factor for the expansion of myeloid-derived suppressor cells (MDSCs) and progression of metastasis (Cao et al., 2014). Although the anti-inflammatory effects of TGF-β are well established, the precise role of BMP signaling in the immune system remains fully uncovered.
Applications of Small-Molecule Bone Morphogenetic Protein Inhibitors in Cancer Treatment
Many researchers have attempted to use BMP type I receptor inhibitors to treat various types of cancers. As mutations in the ACVR1 gene are responsible for the pathogenesis of FOP, and such mutations are also found in patients with DIPG, the development of ALK2-specific inhibitors is expected. The current computational approach reveals small changes in the binding site residue type or side-chain orientation in ALKs, as well as subtle structural modifications of the inhibitors, which can be used to improve the specificity of BMP inhibitors (Alsamarah et al., 2015). Dorsomorphin is a prototype BMP type I receptor inhibitor containing a pyrazolo [1,5-a]-pyrimidine scaffold. Subsequently, more ALK2-selective and metabolically stable inhibitors, LDN-193189 and LDN-212854, were developed (Rooney & Jones, 2021). In addition to pyrazolo [1,5-a]-pyrimidine, other scaffolds have also been identified, such as pyridines, quinazolinones, and pyrazoles. M4K2163, a pyridine-based compound, has been shown to have good permeability in the brain (Rooney & Jones, 2021). Our group recently developed the pyrazole-based compounds RK-59638 and RK-71807 (Sato et al., 2020).
These bioavailable inhibitors have allowed examination of their beneficial effects in various types of mouse tumor models. The therapeutic effects of these inhibitors have been documented for DIPG. Treatment of mice bearing ACVR1 R206H mutation-harboring DIPG cells with LDN-193189 or LDN-214117 extended the survival of host mice compared with vehicle controls (Carvalho et al., 2019). Many reports have also shown that ALK2 inhibitors potently inhibit the formation and progression of other cancers. In breast cancer, treatment of a mouse cancer model with LDN-193189 suppressed tumor-initiating capacity and EMT induction, as well as prolonged tumor latency (Balboni et al., 2013). When MMTV.PyVmT-expressing mice were treated with an osmotic pump containing the BMP type I receptor inhibitor, DMH1, the tumors were less proliferative and more apoptotic, reducing lung metastasis. Simultaneously, DMH1 affects fibroblasts, lymphatic vessels, and macrophages, reducing their tumor-promoting effects (Owens et al., 2015). Our group revealed that intraperitoneal administration of LDN-193189 reduced the Erk MAP kinase signaling pathway in CRC cells, attenuating primary tumor formation in mice-bearing CRC cells (Yokoyama et al., 2017). In HCC, treatment with LDN-212854 repressed ID1 and EpCAM expression in cancer cells in vivo, suggesting that the repression of the BMP-9-induced CSC phenotype was attenuated by the inhibitor (Chen et al., 2021). In brain tumors, ovarian cancer, lung cancer, oral squamous cell carcinoma, endometrial cancer, and melanoma, the therapeutic benefits of ALK2 inhibitors are suggested (Langenfeld et al., 2013; Hao et al., 2014; Hover et al., 2015; Peng et al., 2016; Newman et al., 2018; Yin et al., 2018; Mihajlović et al., 2019; Zhou et al., 2020; Fukuda et al., 2021; Kalal et al., 2021). Our research group recently reported that a BMP type I receptor inhibitor, RK-783, inhibited the growth of ovarian cancer cells in vivo (Fukuda et al., 2020).
As the survival of cancer cells is augmented by BMP signaling, BMPs determine the sensitivity to chemotherapeutic drugs (Camara-Clayette et al., 2013; Bach et al., 2018). ALK2 inhibitors are expected to be used in combination with cytotoxic agents to treat cancers. DMH1 enhances the sensitivity of ovarian cancer cells to cisplatin treatment (Hover et al., 2015). DMH1 reduces the growth of cetuximab-resistant oral squamous cell carcinoma (Yin et al., 2018). LDN-193189 augmented the growth-inhibitory effects of carboplatin (Fukuda et al., 2021).
However, these inhibitors are not entirely specific to ALK2. Among the pyrazolo [1,5-a]-pyrimidine-containing inhibitors, dorsomorphin typically induces autophagy in ovarian cancer cells, whereas LDN-193189 induces ROS-mediated apoptosis in the same cell lines. As this discrepancy is thought to be caused by the off-target effects of each inhibitor, the development of more specific ALK2 inhibitors is required (Ali et al., 2015). In addition, as mentioned above, because BMPs have tumor-suppressive functions under certain conditions, tumor formation or metastasis might be promoted through the inhibition of BMP signaling (Vollaire et al., 2019; Sharma et al., 2021). We should clarify which types of cancer ALK2 inhibitors are effective against.
Targeting Angiogenesis via Inhibition of ALK1 Signaling
To suppress tumor angiogenesis, various strategies have been utilized to inhibit BMP-9/10-ALK1 signaling, such as soluble form receptors, neutralizing antibodies, and small-molecule receptor inhibitors. Dalantercept (ACE-041), a soluble form of ALK1, acts as a ligand trap for BMP-9/10, inhibiting the interactions between BMP-9/10 and ALK1. The therapeutic potential of dalantercept has been demonstrated in various mouse tumor models (Mitchell et al., 2010; Cunha et al., 2015; Hawinkel et al., 2016). Notably, dalantercept inhibits tumor angiogenesis by regulating signaling pathways other than VEGF signaling. Thus, dalantercept is considered a promising inhibitor for treating RCC, in which escape from VEGF-mediated tumor angiogenesis is critical (Philips & Atkins, 2014; Wang et al., 2016). Initial studies have shown that dalantercept is well tolerated in humans. However, clinical trials with patients with RCC have failed to show therapeutic benefits (Bendell et al., 2014; Voss et al., 2017; Voss et al., 2019). Clinical studies on patients with other cancers have revealed that dalantercept has insufficient efficacy in HCC, ovarian cancer, endometrial cancer, and head and neck cancer (Makker et al., 2015; Jimeno et al., 2016; Burger et al., 2018; Abou-Alfa et al., 2019). PF-03446962 is a fully humanized monoclonal antibody that targets and neutralizes human ALK1 (van Meeteren et al., 2012). Its pharmacokinetics and therapeutic benefits were evaluated in a preclinical model, followed by evaluations in humans (Hu-Lowe et al., 2011; Luu et al., 2012; Li et al., 2014). Although the results of a phase I study of PF-0334962 in patients with cancer initially supported further evaluation (Doi et al., 2016; Goff et al., 2016; Simonelli et al., 2016), phase II studies have demonstrated insufficient efficacy or unacceptable toxicity in the treatment of CRC, urothelial cancer, and mesothelioma (Necchi et al., 2014; Wheatley et al., 2016; Clarke et al., 2019). The small-molecule kinase inhibitor K02288 inhibits BMP-9-induced phosphorylation of Smad1/5 in human umbilical vein endothelial cells to reduce both Smad- and Notch-dependent transcriptional responses. K02288 caused dysfunctional vessel formation in a chick chorioallantoic membrane angiogenesis assay (Kerr et al., 2015). It is currently unknown why the inhibition of ALK-1 signaling failed to show clinical effects, and further studies on the in vivo effects of ALK-1 inhibitors on tumor angiogenesis are needed. Additional information will be forthcoming.
Conclusion
In the present article, the diverse effects of BMPs are reviewed based on the latest literatures. As BMPs are considered potentially important therapeutic targets in some cancers, treatments with BMP inhibitors have been attempted. However, favorable results have not always been obtained. BMPs act in a context-dependent manner and become tumor suppressors under certain conditions. It is difficult to understand the fact that conflicting data have been obtained for the same cancers, even in the analyses using same cancer cell lines. The key factor(s) that switch the pro-oncogenic or tumor-suppressive functions of BMPs remains unknown. Different BMPs may act differently on each receptor. In addition, BMPs may act not only on many cancer cells but also on cellular components in the tumor microenvironment, leading to different results in different experimental settings. Thus, discovery of biomarkers which can discriminate the responses of certain cancers to BMPs is required.
Finally, the amounts of different BMPs biologically available in the cancer microenvironment should be considered. In the past, to observe cellular responses, many cancer cells were stimulated with ligands or overexpressed with BMPs. Although these evaluations have greatly contributed to our understanding of the diverse effects of BMPs, they do not always reproduce the roles of BMPs under physiological conditions. Notably, some biological effects of BMPs occur in a concentration-dependent or biphasic manner. In addition, crosstalk between BMPs and other signaling pathways may be important. In particular, crosstalk between BMP signaling and TGF-β signaling, which is a strong determinant of the metastatic phenotype of cancer cells, may be important. BMPs often exert their biological functions by enhancing or counteracting the effects of TGF-β. Therefore, evaluating not only the intensity of BMP signaling but also the intensity of TGF-β signaling may be needed.
Statements
Author contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
Funding
This work was supported by a KAKENHI Grant-in-Aid for Scientific Research on Innovative Area on Integrated Analysis and Regulation of Cellular Diversity from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan (17H06326 to SE and KM); a KAKENHI Grant-in-Aid for Scientific Research (C) from the Japan Society for the Promotion of Science (JSPS) (19K07684 to SE) and Scientific Research (A) (20H00513 to KM); a research program of the Japan Agency for Medical Research and Development (AMED) (grant no. 20ek0109325h0003 to KM); and the Princess Takamatsu Cancer Research Fund (to SE).
Acknowledgments
We are grateful to all laboratory members of KM laboratory at The University of Tokyo.
Conflict of interest
SE and KM were partly supported by Eisai, Co., Ltd.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1
Abou-AlfaG. K.MiksadR. A.TejaniM. A.WilliamsonS.GutierrezM. E.OlowokureO. O.et al (2019). A Phase Ib, Open-Label Study of Dalantercept, an Activin Receptor-like Kinase 1 Ligand Trap, Plus Sorafenib in Advanced Hepatocellular Carcinoma. Oncologist24, 161–e70. 10.1634/theoncologist.2018-0654
2
AliJ. L.LagasseB. J.MinukA. J.LoveA. J.MorayaA. I.LamL.et al (2015). Differential Cellular Responses Induced by Dorsomorphin and LDN-193189 in Chemotherapy-Sensitive and Chemotherapy-Resistant Human Epithelial Ovarian Cancer Cells. Int. J. Cancer136, E455–E469. 10.1002/ijc.29220
3
AlsamarahA.LaCuranA. E.OelschlaegerP.HaoJ.LuoY. (2015). Uncovering Molecular Bases Underlying Bone Morphogenetic Protein Receptor Inhibitor Selectivity. PLoS One10, e0132221. 10.1371/journal.pone.0132221
4
AnttonenM.FärkkiläA.TaurialaH.KauppinenM.MaclaughlinD. T.Unkila-KallioL.et al (2011). Anti-Müllerian Hormone Inhibits Growth of AMH Type II Receptor-Positive Human Ovarian Granulosa Cell Tumor Cells by Activating Apoptosis. Lab. Invest.91, 1605–1614. 10.1038/labinvest.2011.116
5
BachD.-H.LuuT.-T.-T.KimD.AnY. J.ParkS.ParkH. J.et al (2018). BMP4 Upregulation Is Associated with Acquired Drug Resistance and Fatty Acid Metabolism in EGFR-Mutant Non-small-cell Lung Cancer Cells. Mol. Ther. Nucleic Acids12, 817–828. 10.1016/j.omtn.2018.07.016
6
BalboniA. L.HutchinsonJ. A.DeCastroA. J.CherukuriP.LibyK.SpornM. B.et al (2013). ΔNp63α-Mediated Activation of Bone Morphogenetic Protein Signaling Governs Stem Cell Activity and Plasticity in Normal and Malignant Mammary Epithelial Cells. Cancer Res.73, 1020–1030. 10.1158/0008-5472.can-12-2862
7
BaoZ.ZhangC.YanW.LiuY.LiM.ZhangW.et al (2013). BMP4, a Strong Better Prognosis Predictor, Has a Subtype Preference and Cell Development Association in Gliomas. J. Transl. Med.11, 100. 10.1186/1479-5876-11-100
8
BendellJ. C.GordonM. S.HurwitzH. I.JonesS. F.MendelsonD. S.BlobeG. C.et al (2014). Safety, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of Dalantercept, an Activin Receptor-like Kinase-1 Ligand Trap, in Patients with Advanced Cancer. Clin. Cancer Res.20, 480–489. 10.1158/1078-0432.ccr-13-1840
9
BrazilD. P.ChurchR. H.SuraeS.GodsonC.MartinF. (2015). BMP Signalling: Agony and Antagony in the Family. Trends Cell Biol.25, 249–264. 10.1016/j.tcb.2014.12.004
10
BuczkowiczP.HoemanC.RakopoulosP.PajovicS.LetourneauL.DzambaM.et al (2014). Genomic Analysis of Diffuse Intrinsic Pontine Gliomas Identifies Three Molecular Subgroups and Recurrent Activating ACVR1 Mutations. Nat. Genet.46, 451–456. 10.1038/ng.2936
11
BuijsJ. T.van der HorstG.van den HoogenC.CheungH.de RooijB.KroonJ.et al (2012). The BMP2/7 Heterodimer Inhibits the Human Breast Cancer Stem Cell Subpopulation and Bone Metastases Formation. Oncogene31, 2164–2174. 10.1038/onc.2011.400
12
BurgerR. A.DengW.MakkerV.CollinsY.GrayH.DebernardoR.et al (2018). Phase II Evaluation of Dalantercept in the Treatment of Persistent or Recurrent Epithelial Ovarian Cancer: an NRG Oncology/Gynecologic Oncology Group Study. Gynecol. Oncol.150, 466–470. 10.1016/j.ygyno.2018.06.017
13
CajaL.TzavlakiK.DadrasM. S.TanE.-J.HatemG.MaturiN. P.et al (2018). Snail Regulates BMP and TGFβ Pathways to Control the Differentiation Status of Glioma-Initiating Cells. Oncogene37, 2515–2531. 10.1038/s41388-018-0136-0
14
Camara-ClayetteV.KoscielnyS.RouxS.LamyT.BosqJ.BernardM.et al (2013). BMP7 Expression Correlates with Secondary Drug Resistance in Mantle Cell Lymphoma. PLoS One8, e73993. 10.1371/journal.pone.0073993
15
CaoY.SlaneyC. Y.BidwellB. N.ParkerB. S.JohnstoneC. N.RautelaJ.et al (2014). BMP4 Inhibits Breast Cancer Metastasis by Blocking Myeloid-Derived Suppressor Cell Activity. Cancer Res.74, 5091–5102. 10.1158/0008-5472.can-13-3171
16
CarvalhoD.TaylorK. R.OlacireguiN. G.MolinariV.ClarkeM.MackayA.et al (2019). ALK2 Inhibitors Display Beneficial Effects in Preclinical Models of ACVR1 Mutant Diffuse Intrinsic Pontine Glioma. Commun. Biol.2, 156. 10.1038/s42003-019-0420-8
17
ChangC. (2016). Agonists and Antagonists of TGF-β Family Ligands. Cold Spring Harb. Perspect. Biol.8, a021923. 10.1101/cshperspect.a021923
18
ChenH.NioK.YamashitaT.OkadaH.LiR.SudaT.et al (2021). BMP9-ID1 Signaling Promotes EpCAM-Positive Cancer Stem Cell Properties in Hepatocellular Carcinoma. Mol. Oncol.15, 2203–2218. 10.1002/1878-0261.12963
19
ChenJ.-C.YangS.-T.LinC.-Y.HsuC.-J.TsaiC.-H.SuJ.-L.et al (2014). BMP-7 Enhances Cell Migration and αvβ3 Integrin Expression via a C-src-dependent Pathway in Human Chondrosarcoma Cells. PLoS One9, e112636. 10.1371/journal.pone.0112636
20
ChiuC.-Y.KuoK.-K.KuoT.-L.LeeK.-T.ChengK.-H. (2012). The Activation of MEK/ERK Signaling Pathway by Bone Morphogenetic Protein 4 to Increase Hepatocellular Carcinoma Cell Proliferation and Migration. Mol. Cancer Res.10, 415–427. 10.1158/1541-7786.mcr-11-0293
21
ChoiS.YuJ.ParkA.DubonM. J.DoJ.KimY.et al (2019). BMP-4 Enhances Epithelial Mesenchymal Transition and Cancer Stem Cell Properties of Breast Cancer Cells via Notch Signaling. Sci. Rep.9, 11724. 10.1038/s41598-019-48190-5
22
ChoiY. J.KimS. T.ParkK. H.OhS. C.SeoJ. H.ShinS. W.et al (2012). The Serum Bone Morphogenetic Protein-2 Level in Non-small-cell Lung Cancer Patients. Med. Oncol.29, 582–588. 10.1007/s12032-011-9852-9
23
ClarkeJ. M.BlobeG. C.StricklerJ. H.UronisH. E.ZafarS. Y.MorseM.et al (2019). A Phase Ib Study of the Combination Regorafenib with PF-03446962 in Patients with Refractory Metastatic Colorectal Cancer (REGAL-1 Trial). Cancer Chemother. Pharmacol.84, 909–917. 10.1007/s00280-019-03916-0
24
CoffmanL. G.ChoiY.-J.McLeanK.AllenB. L.di MaglianoM. P.BuckanovichR. J. (2016). Human Carcinoma-Associated Mesenchymal Stem Cells Promote Ovarian Cancer Chemotherapy Resistance via a BMP4/HH Signaling Loop. Oncotarget7, 6916–6932. 10.18632/oncotarget.6870
25
CorrensA.ZimmermannL.-M. A.BaldockC.SengleG. (2021). BMP Antagonists in Tissue Development and Disease. Matrix Biol. Plus11, 100071. 10.1016/j.mbplus.2021.100071
26
CortezM. A.MasrorpourF.IvanC.ZhangJ.YounesA. I.LuY.et al (2020). Bone Morphogenetic Protein 7 Promotes Resistance to Immunotherapy. Nat. Commun.11, 4840. 10.1038/s41467-020-18617-z
27
CunhaS. I.BocciM.LövrotJ.EleftheriouN.RoswallP.CorderoE.et al (2015). Endothelial ALK1 Is a Therapeutic Target to Block Metastatic Dissemination of Breast Cancer. Cancer Res.75, 2445–2456. 10.1158/0008-5472.can-14-3706
28
DallasN. A.SamuelS.XiaL.FanF.GrayM. J.LimS. J.et al (2008). Endoglin (CD105): a Marker of Tumor Vasculature and Potential Target for Therapy. Clin. Cancer Res.14, 1931–1937. 10.1158/1078-0432.ccr-07-4478
29
DavisH.RajaE.MiyazonoK.TsubakiharaY.MoustakasA. (2016). Mechanisms of Action of Bone Morphogenetic Proteins in Cancer. Cytokine Growth Factor Rev.27, 81–92. 10.1016/j.cytogfr.2015.11.009
30
DengG.ZengS.QuY.LuoQ.GuoC.YinL.et al (2018). BMP4 Promotes Hepatocellular Carcinoma Proliferation by Autophagy Activation through JNK1-Mediated Bcl-2 Phosphorylation. J. Exp. Clin. Cancer Res.37, 156. 10.1186/s13046-018-0828-x
31
DoiT.LeeK. H.KimT. M.OhtsuA.KimT. Y.IkedaM.et al (2016). A Phase I Study of the Human Anti-activin Receptor-like Kinase 1 Antibody PF -03446962 in Asian Patients with Advanced Solid Tumors. Cancer Med.5, 1454–1463. 10.1002/cam4.724
32
EhataS.YokoyamaY.TakahashiK.MiyazonoK. (2013). Bi-directional Roles of Bone Morphogenetic Proteins in Cancer: Another Molecular Jekyll and Hyde?Pathol. Int.63, 287–296. 10.1111/pin.12067
33
FanY.GuoL.ZhengH.JiC.WangW.SunH. (2020). BMP-9 Is a Novel Marker for Colorectal Tumorigenesis Undergoing the Normal Mucosa-Adenoma-Adenocarcinoma Sequence and Is Associated with Colorectal Cancer Prognosis. Oncol. Lett.19, 271–282. 10.3892/ol.2019.11125
34
FeiZ.-H.YaoC.-Y.YangX.-L.HuangX.-E.MaS.-L. (2013). Serum BMP-2 Up-Regulation as an Indicator of Poor Survival in Advanced Non-small Cell Lung Cancer Patients. Asian Pac. J. Cancer Prev.14, 5293–5299. 10.7314/apjcp.2013.14.9.5293
35
FengP.-C.KeX.-F.KuangH.-L.PanL.-L.YeQ.WuJ.-B. (2019). RETRACTED ARTICLE: BMP2 Secretion from Hepatocellular Carcinoma Cell HepG2 Enhances Angiogenesis and Tumor Growth in Endothelial Cells via Activation of the MAPK/p38 Signaling Pathway. Stem Cell Res. Ther.10, 237. 10.1186/s13287-019-1301-2
36
FontebassoA. M.Papillon-CavanaghS.SchwartzentruberJ.NikbakhtH.GergesN.FisetP.-O.et al (2014). Recurrent Somatic Mutations in ACVR1 in Pediatric Midline High-Grade Astrocytoma. Nat. Genet.46, 462–466. 10.1038/ng.2950
37
FukudaT.FukudaR.MiyazonoK.HeldinC.-H. (2021). Tumor Promoting Effect of BMP Signaling in Endometrial Cancer. Int. J. Mol. Sci.22, 7882. 10.3390/ijms22157882
38
FukudaT.FukudaR.TanabeR.KoinumaD.KoyamaH.HashizumeY.et al (2020). BMP Signaling Is a Therapeutic Target in Ovarian Cancer. Cell Death Discov.6, 139. 10.1038/s41420-020-00377-w
39
GengS.SunB.LuR.WangJ. (2014). Coleusin Factor, a Novel Anticancer Diterpenoid, Inhibits Osteosarcoma Growth by Inducing Bone Morphogenetic Protein-2-dependent Differentiation. Mol. Cancer Ther.13, 1431–1441. 10.1158/1535-7163.mct-13-0934
40
GillJ.ConnollyP.RothM.ChungS. H.ZhangW.PiperdiS.et al (2017). The Effect of Bone Morphogenetic Protein-2 on Osteosarcoma Metastasis. PLoS One12, e0173322. 10.1371/journal.pone.0173322
41
GoffL. W.CohenR. B.BerlinJ. D.de BraudF. G.LyshchikA.NoberascoC.et al (2016). A Phase I Study of the Anti-activin Receptor-like Kinase 1 (ALK-1) Monoclonal Antibody PF-03446962 in Patients with Advanced Solid Tumors. Clin. Cancer Res.22, 2146–2154. 10.1158/1078-0432.ccr-15-1622
42
González-GómezP.Crecente-CampoJ.ZahoneroC.de la FuenteM.Hernández-LaínA.MiraH.et al (2015). Controlled Release Microspheres Loaded with BMP7 Suppress Primary Tumors from Human Glioblastoma. Oncotarget6, 10950–10963. 10.18632/oncotarget.3459
43
GotoK.KamiyaY.ImamuraT.MiyazonoK.MiyazawaK. (2007). Selective Inhibitory Effects of Smad6 on Bone Morphogenetic Protein Type I Receptors. J. Biol. Chem.282, 20603–20611. 10.1074/jbc.m702100200
44
GuanH.LiJ.SunR.LiuW.FengM.MaH.et al (2019). Expression of BMP7 in Ovarian Cancer and Biological Effect of BMP7 Knockdown on Ovarian Cancer Cells. Onco Targets Ther.12, 7897–7909. 10.2147/ott.s217975
45
Guo DD.HuangJ.GongJ. (2012). Bone Morphogenetic Protein 4 (BMP4) Is Required for Migration and Invasion of Breast Cancer. Mol. Cell. Biochem.363, 179–190. 10.1007/s11010-011-1170-1
46
GuoJ.GuoM.ZhengJ. (2021). Inhibition of Bone Morphogenetic Protein 2 Suppresses the Stemness Maintenance of Cancer Stem Cells in Hepatocellular Carcinoma via the MAPK/ERK Pathway. Cancer Manag. Res.13, 773–785. 10.2147/cmar.s281969
47
Guo XX.XiongL.ZouL.ZhaoJ. (2012). Upregulation of Bone Morphogenetic Protein 4 Is Associated with Poor Prognosis in Patients with Hepatocellular Carcinoma. Pathol. Oncol. Res.18, 635–640. 10.1007/s12253-011-9488-2
48
HaoJ.LeeR.ChangA.FanJ.LabibC.ParsaC.et al (2014). DMH1, a Small Molecule Inhibitor of BMP Type I Receptors, Suppresses Growth and Invasion of Lung Cancer. PLoS One9, e90748. 10.1371/journal.pone.0090748
49
HatsellS. J.IdoneV.WolkenD. M.HuangL.KimH. J.WangL.et al (2015). ACVR1R206H Receptor Mutation Causes Fibrodysplasia Ossificans Progressiva by Imparting Responsiveness to Activin A. Sci. Transl. Med.7, 303ra137. 10.1126/scitranslmed.aac4358
50
HawinkelsL. J. A. C.de VinuesaA. G.PaauweM.Kruithof-de JulioM.WiercinskaE.PardaliE.et al (2016). Activin Receptor-like Kinase 1 Ligand Trap Reduces Microvascular Density and Improves Chemotherapy Efficiency to Various Solid Tumors. Clin. Cancer Res.22, 96–106. 10.1158/1078-0432.ccr-15-0743
51
HerreraB.García-ÁlvaroM.CruzS.WalshP.FernándezM.RonceroC.et al (2013). BMP9 Is a Proliferative and Survival Factor for Human Hepatocellular Carcinoma Cells. PLoS One8, e69535. 10.1371/journal.pone.0069535
52
HoemanC. M.CorderoF. J.HuG.MisuracaK.RomeroM. M.CardonaH. J.et al (2019). ACVR1 R206H Cooperates with H3.1K27M in Promoting Diffuse Intrinsic Pontine Glioma Pathogenesis. Nat. Commun.10, 1023. 10.1038/s41467-019-08823-9
53
HoverL. D.YoungC. D.BholaN. E.WilsonA. J.KhabeleD.HongC. C.et al (2015). Small Molecule Inhibitor of the Bone Morphogenetic Protein Pathway DMH1 Reduces Ovarian Cancer Cell Growth. Cancer Lett.368, 79–87. 10.1016/j.canlet.2015.07.032
54
HuY.YuL.XiaF.LiangF.ChengC.HuangY.et al (2021). Expression of Bone Morphogenetic Protein 10 in Cases with Endometrial Carcinoma and its Clinical Significance. Clin. Transl. Oncol.23, 1711–1716. 10.1007/s12094-021-02572-2
55
Hu-LoweD. D.ChenE.ZhangL.WatsonK. D.MancusoP.LappinP.et al (2011). Targeting Activin Receptor-like Kinase 1 Inhibits Angiogenesis and Tumorigenesis through a Mechanism of Action Complementary to Anti-VEGF Therapies. Cancer Res.71, 1362–1373. 10.1158/0008-5472.can-10-1451
56
HuangF.CaoY.WuG.ChenJ.CaihongWangLinW.LinW.et al (2020). BMP2 Signalling Activation Enhances Bone Metastases of Non-small Cell Lung Cancer. J. Cell. Mol. Med.24, 10768–10784. 10.1111/jcmm.15702
57
HuangP.ChenA.HeW.LiZ.ZhangG.LiuZ.et al (2017). BMP-2 Induces EMT and Breast Cancer Stemness through Rb and CD44. Cell Death Discov.3, 17039. 10.1038/cddiscovery.2017.39
58
IhleC. L.StraignD. M.ProveraM. D.NovitskiyS. V.OwensP. (2020). Loss of Myeloid BMPR1a Alters Differentiation and Reduces Mouse Prostate Cancer Growth. Front. Oncol.10, 357. 10.3389/fonc.2020.00357
59
JiaY.WangZ.ZangA.JiaoS.ChenS.FuY. (2016). Tetramethylpyrazine Inhibits Tumor Growth of Lung Cancer through Disrupting Angiogenesis via BMP/Smad/Id-1 Signaling. Int. J. Oncol.48, 2079–2086. 10.3892/ijo.2016.3443
60
JimenoA.PosnerM. R.WirthL. J.SabaN. F.CohenR. B.PopaE. C.et al (2016). A Phase 2 Study of Dalantercept, an Activin Receptor-like Kinase-1 Ligand Trap, in Patients with Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck. Cancer122, 3641–3649. 10.1002/cncr.30317
61
JinX.NieE.ZhouX.ZengA.YuT.ZhiT.et al (2017). Fstl1 Promotes Glioma Growth through the BMP4/Smad1/5/8 Signaling Pathway. Biochem.44, 1616–1628. 10.1159/000485759
62
KalalB. S.ModiP. K.UpadhyaD.SahaP.PrasadT. S. K.PaiV. R. (2021). Inhibition of Bone Morphogenetic Proteins Signaling Suppresses Metastasis Melanoma: a Proteomics Approach. Am. J. Transl. Res.13, 11081–11093.
63
KatagiriT.WatabeT. (2016). Bone Morphogenetic Proteins. Cold Spring Harb. Perspect. Biol.8, a021899. 10.1101/cshperspect.a021899
64
KatsunoY.HanyuA.KandaH.IshikawaY.AkiyamaF.IwaseT.et al (2008). Bone Morphogenetic Protein Signaling Enhances Invasion and Bone Metastasis of Breast Cancer Cells through Smad Pathway. Oncogene27, 6322–6333. 10.1038/onc.2008.232
65
KerrG.SheldonH.ChaikuadA.AlfanoI.von DelftF.BullockA. N.et al (2015). A Small Molecule Targeting ALK1 Prevents Notch Cooperativity and Inhibits Functional Angiogenesis. Angiogenesis18, 209–217. 10.1007/s10456-014-9457-y
66
KhammanivongA.GopalakrishnanR.DickersonE. B. (2014). SMURF1 Silencing Diminishes a CD44-High Cancer Stem Cell-like Population in Head and Neck Squamous Cell Carcinoma. Mol. Cancer13, 260. 10.1186/1476-4598-13-260
67
KimS. M.YeS.RahS.-Y.ParkB. H.WangH.KimJ.-R.et al (2016). RhBMP-2 Activates Hippo Signaling through RASSF1 in Esophageal Cancer Cells. Sci. Rep.6, 26821. 10.1038/srep26821
68
KuczmaM.KurczewskaA.KrajP. (2014). Modulation of Bone Morphogenic Protein Signaling in T-Cells for Cancer Immunotherapy. J. Immunotoxicol.11, 319–327. 10.3109/1547691x.2013.864736
69
LangenfeldE.HongC. C.LankeG.LangenfeldJ. (2013). Bone Morphogenetic Protein Type I Receptor Antagonists Decrease Growth and Induce Cell Death of Lung Cancer Cell Lines. PLoS One8, e61256. 10.1371/journal.pone.0061256
70
LeeJ.SonM. J.WoolardK.DoninN. M.LiA.ChengC. H.et al (2008). Epigenetic-mediated Dysfunction of the Bone Morphogenetic Protein Pathway Inhibits Differentiation of Glioblastoma-Initiating Cells. Cancer Cell13, 69–80. 10.1016/j.ccr.2007.12.005
71
LeinhäuserI.RichterA.LeeM.HöfigI.AnastasovN.FendF.et al (2015). Oncogenic Features of the Bone Morphogenic Protein 7 (BMP7) in Pheochromocytoma. Oncotarget6, 39111–39126.
72
LiL.GardnerI.DostalekM.JameiM. (2014). Simulation of Monoclonal Antibody Pharmacokinetics in HumansUsing a Minimal Physiologically Based Model. AAPS J.16, 1097–1109. 10.1208/s12248-014-9640-5
73
LiQ.GuX.WengH.GhafooryS.LiuY.FengT.et al (2013). Bone Morphogenetic Protein-9 Induces Epithelial to Mesenchymal Transition in Hepatocellular Carcinoma Cells. Cancer Sci.104, 398–408. 10.1111/cas.12093
74
LiS.DaiH.HeY.PengS.ZhuT.WuY.et al (2018). BMP9 Inhibits the Growth of Breast Cancer Cells by Downregulation of the PI3K/Akt Signaling Pathway. Oncol. Rep.40, 1743–1751. 10.3892/or.2018.6572
75
LiX.SunB.ZhaoX.AnJ.ZhangY.GuQ.et al (2020). Function of BMP4 in the Formation of Vasculogenic Mimicry in Hepatocellular Carcinoma. J. Cancer11, 2560–2571. 10.7150/jca.40558
76
LiuC.-H.TangW.-C.SiaP.HuangC.-C.YangP.-M.WuM.-H.et al (2015). Berberine Inhibits the Metastatic Ability of Prostate Cancer Cells by Suppressing Epithelial-To-Mesenchymal Transition (EMT)-associated Genes with Predictive and Prognostic Relevance. Int. J. Med. Sci.12, 63–71. 10.7150/ijms.9982
77
LiuY.ChenJ.YangY.ZhangL.JiangW. G. (2012). Μolecular Impact of Bone Morphogenetic Protein 7, on Lung Cancer Cells and its Clinical Significance. Int. J. Mol. Med.29, 1016–1024. 10.3892/ijmm.2012.948
78
LuuK. T.BergqvistS.ChenE.Hu-LoweD.KraynovE. (2012). A Model-Based Approach to Predicting the Human Pharmacokinetics of a Monoclonal Antibody Exhibiting Target-Mediated Drug Disposition. J. Pharmacol. Exp. Ther.341, 702–708. 10.1124/jpet.112.191999
79
MaJ.ZengS.ZhangY.DengG.QuY.GuoC.et al (2017). BMP4 Enhances Hepatocellular Carcinoma Proliferation by Promoting Cell Cycle Progression via ID2/CDKN1B Signaling. Mol. Carcinog.56, 2279–2289. 10.1002/mc.22681
80
MaegdefrauU.BosserhoffA.-K. (2012). BMP Activated Smad Signaling Strongly Promotes Migration and Invasion of Hepatocellular Carcinoma Cells. Exp. Mol. Pathology92, 74–81. 10.1016/j.yexmp.2011.10.004
81
MakkerV.FiliaciV. L.ChenL.-m.DarusC. J.KendrickJ. E.SuttonG.et al (2015). Phase II Evaluation of Dalantercept, a Soluble Recombinant Activin Receptor-like Kinase 1 (ALK1) Receptor Fusion Protein, for the Treatment of Recurrent or Persistent Endometrial Cancer: an NRG Oncology/Gynecologic Oncology Group Study 0229N. Gynecol. Oncol.138, 24–29. 10.1016/j.ygyno.2015.04.006
82
ManoY.YoshioS.ShojiH.TomonariS.AokiY.AoyanagiN.et al (2019). Bone Morphogenetic Protein 4 Provides Cancer-Supportive Phenotypes to Liver Fibroblasts in Patients with Hepatocellular Carcinoma. J. Gastroenterol.54, 1007–1018. 10.1007/s00535-019-01579-5
83
MartínezV. G.RubioC.Martínez-FernándezM.SegoviaC.López-CalderónF.GarínM. I.et al (2017). BMP4 Induces M2 Macrophage Polarization and Favors Tumor Progression in Bladder Cancer. Clin. Cancer Res.23, 7388–7399.
84
MegumiK.IshigamiS.UchikadoY.KitaY.OkumuraH.MatsumotoM.et al (2012). Clinicopathological Significance of BMP7 Expression in Esophageal Squamous Cell Carcinoma. Ann. Surg. Oncol.19, 2066–2071. 10.1245/s10434-011-2024-5
85
MihajlovićJ.DiehlL. A. M.HochhausA.ClementJ. H. (2019). Inhibition of Bone Morphogenetic Protein Signaling Reduces Viability, Growth and Migratory Potential of Non-small Cell Lung Carcinoma Cells. J. Cancer Res. Clin. Oncol.145, 2675–2687. 10.1007/s00432-019-03026-7
86
MitchellD.PobreE. G.MulivorA. W.GrinbergA. V.CastonguayR.MonnellT. E.et al (2010). ALK1-Fc Inhibits Multiple Mediators of Angiogenesis and Suppresses Tumor Growth. Mol. Cancer Ther.9, 379–388. 10.1158/1535-7163.mct-09-0650
87
MitsuiY.HirataH.ArichiN.HirakiM.YasumotoH.ChangI.et al (2015). Inactivation of Bone Morphogenetic Protein 2 May Predict Clinical Outcome and Poor Overall Survival for Renal Cell Carcinoma through Epigenetic Pathways. Oncotarget6, 9577–9591. 10.18632/oncotarget.3445
88
MiuraT.IshiguroM.IshikawaT.OkazakiS.BabaH.KikuchiA.et al (2020). Methylation of Bone Morphogenetic Protein 2 Is Associated with Poor Prognosis in Colorectal Cancer. Oncol. Lett.19, 229–238. 10.3892/ol.2019.11091
89
MiyazakiH.WatabeT.KitamuraT.MiyazonoK. (2004). BMP Signals Inhibit Proliferation and In Vivo Tumor Growth of Androgen-Insensitive Prostate Carcinoma Cells. Oncogene23, 9326–9335. 10.1038/sj.onc.1208127
90
MiyazawaK.MiyazonoK. (2017). Regulation of TGF-β Family Signaling by Inhibitory Smads. Cold Spring Harb. Perspect. Biol.9, a022095. 10.1101/cshperspect.a022095
91
MiyazonoK.KamiyaY.MorikawaM. (2010). Bone Morphogenetic Protein Receptors and Signal Transduction. J. Biochem.147, 35–51. 10.1093/jb/mvp148
92
MockK.PrecaB.-T.BrummerT.BrabletzS.StemmlerM. P.BrabletzT. (2015). The EMT-Activator ZEB1 Induces Bone Metastasis Associated Genes Including BMP-Inhibitors. Oncotarget6, 14399–14412. 10.18632/oncotarget.3882
93
MomoiY.NishidaJ.MiyakuniK.KurodaM.KubotaS. I.MiyazonoK.et al (2021). Heterogenous Expression of Endoglin Marks Advanced Renal Cancer with Distinct Tumor Microenvironment Fitness. Cancer Sci.112, 3136–3149. 10.1111/cas.15007
94
MorikawaM.DerynckR.MiyazonoK. (2016). TGF-β and the TGF-β Family: Context-dependent Roles in Cell and Tissue Physiology. Cold Spring Harb. Perspect. Biol.8, a021873. 10.1101/cshperspect.a021873
95
NayakS.MahenthiranA.YangY.McClendonM.Mania-FarnellB.JamesC. D.et al (2020). Bone Morphogenetic Protein 4 Targeting Glioma Stem-like Cells for Malignant Glioma Treatment: Latest Advances and Implications for Clinical Application. Cancers12, 516. 10.3390/cancers12020516
96
NecchiA.GiannatempoP.MarianiL.FarèE.RaggiD.PennatiM.et al (2014). PF-03446962, a Fully-Human Monoclonal Antibody against Transforming Growth-Factor β (TGFβ) Receptor ALK1, in Pre-treated Patients with Urothelial Cancer: an Open Label, Single-Group, Phase 2 Trial. Invest. New Drugs32, 555–560. 10.1007/s10637-014-0074-9
97
NewmanJ. H.AugeriD. J.NeMoyerR.MalhotraJ.LangenfeldE.ChessonC. B.et al (2018). Novel Bone Morphogenetic Protein Receptor Inhibitor JL5 Suppresses Tumor Cell Survival Signaling and Induces Regression of Human Lung Cancer. Oncogene37, 3672–3685. 10.1038/s41388-018-0156-9
98
NikbakhtH.PanditharatnaE.MikaelL. G.LiR.GaydenT.OsmondM.et al (2016). Spatial and Temporal Homogeneity of Driver Mutations in Diffuse Intrinsic Pontine Glioma. Nat. Commun.7, 11185. 10.1038/ncomms11185
99
NishimoriH.EhataS.SuzukiH. I.KatsunoY.MiyazonoK. (2012). Prostate Cancer Cells and Bone Stromal Cells Mutually Interact with Each Other through Bone Morphogenetic Protein-Mediated Signals. J. Biol. Chem.287, 20037–20046. 10.1074/jbc.m112.353094
100
OlsenO. E.WaderK. F.MisundK.VåtsveenT. K.RøT. B.MylinA. K.et al (2014). Bone Morphogenetic Protein-9 Suppresses Growth of Myeloma Cells by Signaling through ALK2 but Is Inhibited by Endoglin. Blood Cancer J.4, e196. 10.1038/bcj.2014.16
101
OuahoudS.VoorneveldP. W.van der BurgL. R. A.de Jonge-MullerE. S. M.SchoonderwoerdM. J. A.PaauweM.et al (2020). Bidirectional Tumor/stroma Crosstalk Promotes Metastasis in Mesenchymal Colorectal Cancer. Oncogene39, 2453–2466. 10.1038/s41388-020-1157-z
102
OwensP.PickupM. W.NovitskiyS. V.GiltnaneJ. M.GorskaA. E.HopkinsC. R.et al (2015). Inhibition of BMP Signaling Suppresses Metastasis in Mammary Cancer. Oncogene34, 2437–2449. 10.1038/onc.2014.189
103
PengJ.YoshiokaY.MandaiM.MatsumuraN.BabaT.YamaguchiK.et al (2016). The BMP Signaling Pathway Leads to Enhanced Proliferation in Serous Ovarian Cancer-A Potential Therapeutic Target. Mol. Carcinog.55, 335–345. 10.1002/mc.22283
104
PhilipsG. K.AtkinsM. B. (2014). New Agents and New Targets for Renal Cell Carcinoma. Am. Soc. Clin. Oncol. Educ. Book, e222–e227. 10.14694/edbook_am.2014.34.e222
105
PiccirilloS. G. M.ReynoldsB. A.ZanettiN.LamorteG.BindaE.BroggiG.et al (2006). Bone Morphogenetic Proteins Inhibit the Tumorigenic Potential of Human Brain Tumour-Initiating Cells. Nature444, 761–765. 10.1038/nature05349
106
PickupM. W.HoverL. D.GuoY.GorskaA. E.ChytilA.NovitskiyS. V.et al (2015). Deletion of the BMP Receptor BMPR1a Impairs Mammary Tumor Formation and Metastasis. Oncotarget6, 22890–22904. 10.18632/oncotarget.4413
107
RajaE.KomuroA.TanabeR.SakaiS.InoY.SaitoN.et al (2017). Bone Morphogenetic Protein Signaling Mediated by ALK-2 and DLX2 Regulates Apoptosis in Glioma-Initiating Cells. Oncogene36, 4963–4974. 10.1038/onc.2017.112
108
RajaE.MorikawaM.NishidaJ.TanabeR.TakahashiK.SeehermanH. J.et al (2019). Tyrosine Kinase Eph Receptor A6 Sensitizes Glioma-Initiating Cells towards Bone Morphogenetic Protein-Induced Apoptosis. Cancer Sci.110, 3486–3496. 10.1111/cas.14187
109
Reguera-NuñezE.RocaC.HardyE.de la FuenteM.CsabaN.Garcia-FuentesM. (2014). Implantable Controlled Release Devices for BMP-7 Delivery and Suppression of Glioblastoma Initiating Cells. Biomaterials35, 2859–2867. 10.1016/j.biomaterials.2013.12.001
110
RenW.LiuY.WanS.FeiC.WangW.ChenY.et al (2014a). BMP9 Inhibits Proliferation and Metastasis of HER2-Positive SK-BR-3 Breast Cancer Cells through ERK1/2 and PI3K/AKT Pathways. PLoS One9, e96816. 10.1371/journal.pone.0096816
111
RenW.SunX.WangK.FengH.LiuY.FeiC.et al (2014b). BMP9 Inhibits the Bone Metastasis of Breast Cancer Cells by Downregulating CCN2 (Connective Tissue Growth Factor, CTGF) Expression. Mol. Biol. Rep.41, 1373–1383. 10.1007/s11033-013-2982-8
112
RomagnoliM.BelguiseK.YuZ.WangX.Landesman-BollagE.SeldinD. C.et al (2012). The Epithelial-To-Mesenchymal Transition Induced by TGF-β1 Is Mediated by Blimp-1-dependent Repression of BMP-5. Cancer Res.72, 6268–6278. 10.1158/0008-5472.can-12-2270
113
RooneyL.JonesC. (2021). Recent Advances in ALK2 Inhibitors. ACS Omega6, 20729–20734. 10.1021/acsomega.1c02983
114
Sanchez-DuffhuesG.WilliamsE.GoumansM.-J.HeldinC.-H.ten DijkeP. (2020). Bone Morphogenetic Protein Receptors: Structure, Function and Targeting by Selective Small Molecule Kinase Inhibitors. Bone138, 115472. 10.1016/j.bone.2020.115472
115
SandersA. J.YeL.LiJ.MasonM. D.JiangW. G. (2014). Tumour Angiogenesis and Repulsive Guidance Molecule B: A Role in HGF- and BMP-7-Mediated Angiogenesis. Int. J. Oncol.45, 1304–1312. 10.3892/ijo.2014.2508
116
SatoT.SekimataK.SakaiN.WatanabeH.Mishima-TsumagariC.TaguriT.et al (2020). Structural Basis of Activin Receptor-like Kinase 2 (R206H) Inhibition by Bis-Heteroaryl Pyrazole-Based Inhibitors for the Treatment of Fibrodysplasia Ossificans Progressiva Identified by the Integration of Ligand-Based and Structure-Based Drug Design Approaches. ACS Omega5, 11411–11423. 10.1021/acsomega.9b04245
117
SavaryK.CaglayanD.CajaL.TzavlakiK.Bin NayeemS.BergströmT.et al (2013). Snail Depletes the Tumorigenic Potential of Glioblastoma. Oncogene32, 5409–5420. 10.1038/onc.2013.67
118
SconocchiaT.SconocchiaG. (2021). Regulation of the Immune System in Health and Disease by Members of the Bone Morphogenetic Protein Family. Front. Immunol.12, 802346. 10.3389/fimmu.2021.802346
119
SerraoA.JenkinsL. M.ChumanevichA. A.HorstB.LiangJ.GatzaM. L.et al (2018). Mediator Kinase CDK8/CDK19 Drives YAP1-dependent BMP4-Induced EMT in Cancer. Oncogene37, 4792–4808. 10.1038/s41388-018-0316-y
120
SharmaR.GogoiG.SaikiaS.SharmaA.KalitaD. J.SarmaA.et al (2021). BMP4 Enhances Anoikis Resistance and Chemoresistance of Breast Cancer Cells through Canonical BMP Signaling. J. Cell Commun. Signal.16, 191–205. 10.1007/s12079-021-00649-9
121
ShiraiY.-t.EhataS.YashiroM.YanagiharaK.HirakawaK.MiyazonoK. (2011). Bone Morphogenetic Protein-2 and -4 Play Tumor Suppressive Roles in Human Diffuse-type Gastric Carcinoma. Am. J. Pathology179, 2920–2930. 10.1016/j.ajpath.2011.08.022
122
ShoreE. M.XuM.FeldmanG. J.FenstermacherD. A.ChoT.-J.ChoiI. H.et al (2006). A Recurrent Mutation in the BMP Type I Receptor ACVR1 Causes Inherited and Sporadic Fibrodysplasia Ossificans Progressiva. Nat. Genet.38, 525–527. 10.1038/ng1783
123
SimonelliM.ZucaliP.SantoroA.ThomasM. B.de BraudF. G.BorghaeiH.et al (2016). Phase I Study of PF-03446962, a Fully Human Monoclonal Antibody against Activin Receptor-like Kinase-1, in Patients with Hepatocellular Carcinoma. Ann. Oncol.27, 1782–1787. 10.1093/annonc/mdw240
124
SungN. J.KimN. H.SurhY.-J.ParkS.-A. (2020). Gremlin-1 Promotes Metastasis of Breast Cancer Cells by Activating STAT3-MMP13 Signaling Pathway. Int. J. Mol. Sci.21, 9227. 10.3390/ijms21239227
125
SuzukiY.OhgaN.MorishitaY.HidaK.MiyazonoK.WatabeT. (2010). BMP-9 Induces Proliferation of Multiple Types of Endothelial Cells In Vitro and In Vivo. J. Cell Sci.123, 1684–1692. 10.1242/jcs.061556
126
TaeB. S.ChoS.KimH. C.KimC. H.KangS. H.LeeJ. G.et al (2018). Decreased Expression of Bone Morphogenetic Protein-2 Is Correlated with Biochemical Recurrence in Prostate Cancer: Immunohistochemical Analysis. Sci. Rep.8, 10748. 10.1038/s41598-018-28566-9
127
TaguchiL.MiyakuniK.MorishitaY.MorikawaT.FukayamaM.MiyazonoK.et al (2019). c-Ski Accelerates Renal Cancer Progression by Attenuating Transforming Growth Factor β Signaling. Cancer Sci.110, 2063–2074. 10.1111/cas.14018
128
TanabeR.MiyazonoK.TodoT.SaitoN.IwataC.KomuroA.et al (2022). PRRX1 Induced by BMP Signaling Decreases Tumorigenesis by Epigenetically Regulating Glioma-Initiating Cell Properties via DNA Methyltransferase 3A. Mol. Oncol.16, 269–288. 10.1002/1878-0261.13051
129
TarragonaM.PavlovicM.Arnal-EstapéA.UrosevicJ.MoralesM.GuiuM.et al (2012). Identification of NOG as a Specific Breast Cancer Bone Metastasis-Supporting Gene. J. Biol. Chem.287, 21346–21355. 10.1074/jbc.m112.355834
130
TaylorK. R.MackayA.TruffauxN.ButterfieldY. S.MorozovaO.PhilippeC.et al (2014). Recurrent Activating ACVR1 Mutations in Diffuse Intrinsic Pontine Glioma. Nat. Genet.46, 457–461. 10.1038/ng.2925
131
TsaiC.-L.TsaiC.-N.LinC.-Y.ChenH.-W.LeeY.-S.ChaoA.et al (2012). Secreted Stress-Induced Phosphoprotein 1 Activates the ALK2-SMAD Signaling Pathways and Promotes Cell Proliferation of Ovarian Cancer Cells. Cell Rep.2, 283–293. 10.1016/j.celrep.2012.07.002
132
TsuchidaR.OsawaT.WangF.NishiiR.DasB.TsuchidaS.et al (2014). BMP4/Thrombospondin-1 Loop Paracrinically Inhibits Tumor Angiogenesis and Suppresses the Growth of Solid Tumors. Oncogene33, 3803–3811. 10.1038/onc.2013.358
133
TsukamotoS.MizutaT.FujimotoM.OhteS.OsawaK.MiyamotoA.et al (2014). Smad9 Is a New Type of Transcriptional Regulator in Bone Morphogenetic Protein Signaling. Sci. Rep.4, 7596. 10.1038/srep07596
134
ValenciaJ.M. Fernández-SevillaL.SacedónR.JiménezE.VicenteA.et al (2019). Acute Lymphoblastic Leukaemia Cells Impair Dendritic Cell and Macrophage Differentiation: Role of BMP4. Cells8, 722. 10.3390/cells8070722
135
van MeeterenL. A.ThorikayM.BergqvistS.PardaliE.Gallo StampinoC.Hu-LoweD.et al (2012). Anti-human Activin Receptor-like Kinase 1 (ALK1) Antibody Attenuates Bone Morphogenetic Protein 9 (BMP9)-Induced ALK1 Signaling and Interferes with Endothelial Cell Sprouting. J. Biol. Chem.287, 18551–18561. 10.1074/jbc.m111.338103
136
VeschiV.MangiapaneL. R.NicotraA.Di FrancoS.ScavoE.ApuzzoT.et al (2020). Targeting Chemoresistant Colorectal Cancer via Systemic Administration of a BMP7 Variant. Oncogene39, 987–1003. 10.1038/s41388-019-1047-4
137
VollaireJ.Machuca-GayetI.LavaudJ.BellangerA.BouazzaL.El MoghrabiS.et al (2019). The Bone Morphogenetic Protein Signaling Inhibitor LDN-193189 Enhances Metastasis Development in Mice. Front. Pharmacol.10, 667. 10.3389/fphar.2019.00667
138
VoorneveldP. W.KodachL. L.JacobsR. J.LivN.ZonnevylleA. C.HoogenboomJ. P.et al (2014). Loss of SMAD4 Alters BMP Signaling to Promote Colorectal Cancer Cell Metastasis via Activation of Rho and ROCK. Gastroenterology147, 196–208. 10.1053/j.gastro.2014.03.052
139
VossM. H.BhattR. S.PlimackE. R.RiniB. I.AlterR. S.BeckJ. T.et al (2017). The DART Study: Results from the Dose-Escalation and Expansion Cohorts Evaluating the Combination of Dalantercept Plus Axitinib in Advanced Renal Cell Carcinoma. Clin. Cancer Res.23, 3557–3565. 10.1158/1078-0432.ccr-16-2395
140
VossM. H.BhattR. S.VogelzangN. J.FishmanM.AlterR. S.RiniB. I.et al (2019). A Phase 2, Randomized Trial Evaluating the Combination of Dalantercept Plus Axitinib in Patients with Advanced Clear Cell Renal Cell Carcinoma. Cancer125, 2400–2408. 10.1002/cncr.32061
141
WangL.DingQ.ZhaoL.PanY.SongZ.QinY.et al (2018). Decreased BMP-7 and P-Smad1/5/8 Expression, and Increased Levels of Gremlin in Hepatocellular Carcinoma. Oncol. Lett.16, 2113–2118. 10.3892/ol.2018.8918
142
WangL.ParkP.La MarcaF.ThanK. D.LinC.-Y. (2015). BMP-2 Inhibits Tumor-Initiating Ability in Human Renal Cancer Stem Cells and Induces Bone Formation. J. Cancer Res. Clin. Oncol.141, 1013–1024. 10.1007/s00432-014-1883-0
143
WangM.-H.ZhouX.-M.ZhangM.-Y.ShiL.XiaoR.-W.ZengL.-S.et al (2017). BMP2 Promotes Proliferation and Invasion of Nasopharyngeal Carcinoma Cells via mTORC1 Pathway. Aging9, 1326–1340. 10.18632/aging.101230
144
WangX.SolbanN.KhannaP.CalleaM.SongJ.AlsopD. C.et al (2016). Inhibition of ALK1 Signaling with Dalantercept Combined with VEGFR TKI Leads to Tumor Stasis in Renal Cell Carcinoma. Oncotarget7, 41857–41869. 10.18632/oncotarget.9621
145
Wheatley-PriceP.ChuQ.BonomiM.SeelyJ.GuptaA.GossG.et al (2016). A Phase II Study of PF-03446962 in Patients with Advanced Malignant Pleural Mesothelioma. CCTG Trial IND.207. J. Thorac. Oncol.11, 2018–2021. 10.1016/j.jtho.2016.06.024
146
WhissellG.MontagniE.MartinelliP.Hernando-MomblonaX.SevillanoM.JungP.et al (2014). The Transcription Factor GATA6 Enables Self-Renewal of Colon Adenoma Stem Cells by Repressing BMP Gene Expression. Nat. Cell Biol.16, 695–707. 10.1038/ncb2992
147
WozneyJ. M.RosenV.CelesteA. J.MitsockL. M.WhittersM. J.KrizR. W.et al (1988). Novel Regulators of Bone Formation: Molecular Clones and Activities. Science242, 1528–1534. 10.1126/science.3201241
148
WuG.DiazA. K.PaughB. S.RankinS. L.JuB.LiY.et al (2014). The Genomic Landscape of Diffuse Intrinsic Pontine Glioma and Pediatric Non-brainstem High-Grade Glioma. Nat. Genet.46, 444–450. 10.1038/ng.2938
149
XiongQ.WangX.WangL.HuangY.TianX.FanY.et al (2018). BMP-2 Inhibits Lung Metastasis of Osteosarcoma: an Early Investigation Using an Orthotopic Model. Onco Targets Ther.11, 7543–7553. 10.2147/ott.s176724
150
XuG.TangS.YangJ.ChenK.KangJ.ZhaoG.et al (2013). BMP7 Expression in Esophageal Squamous Cell Carcinoma and its Potential Role in Modulating Metastasis. Dig. Dis. Sci.58, 1871–1879. 10.1007/s10620-013-2611-3
151
YahiroY.MaedaS.ShinoharaN.JokojiG.SakumaD.SetoguchiT.et al (2019). PEG10 Counteracts Signaling Pathways of TGF-β and BMP to Regulate Growth, Motility and Invasion of SW1353 Chondrosarcoma Cells. J. Bone Miner. Metab.37, 441–454. 10.1007/s00774-018-0946-8
152
YanG.DaiM.ZhangC.PouletS.MoamerA.WangN.et al (2021). TGFβ/Cyclin D1/Smad-Mediated Inhibition of BMP4 Promotes Breast Cancer Stem Cell Self-Renewal Activity. Oncogenesis10, 21. 10.1038/s41389-021-00310-5
153
YanK.WuQ.YanD. H.LeeC. H.RahimN.TritschlerI.et al (2014). Glioma Cancer Stem Cells Secrete Gremlin1 to Promote Their Maintenance within the Tumor Hierarchy. Genes Dev.28, 1085–1100. 10.1101/gad.235515.113
154
YinJ.JungJ.-E.ChoiS. I.KimS. S.OhY. T.KimT.-H.et al (2018). Inhibition of BMP Signaling Overcomes Acquired Resistance to Cetuximab in Oral Squamous Cell Carcinomas. Cancer Lett.414, 181–189. 10.1016/j.canlet.2017.11.013
155
YokoyamaY.WatanabeT.TamuraY.HashizumeY.MiyazonoK.EhataS. (2017). Autocrine BMP-4 Signaling Is a Therapeutic Target in Colorectal Cancer. Cancer Res.77, 4026–4038. 10.1158/0008-5472.can-17-0112
156
YoshimatsuY.LeeY. G.AkatsuY.TaguchiL.SuzukiH. I.CunhaS. I.et al (2013). Bone Morphogenetic Protein-9 Inhibits Lymphatic Vessel Formation via Activin Receptor-like Kinase 1 during Development and Cancer Progression. Proc. Natl. Acad. Sci. U.S.A.110, 18940–18945. 10.1073/pnas.1310479110
157
YuanY.-M.MaN.ZhangE.-B.ChenT.-W.JiangH.YinF.-F.et al (2019). BMP10 Suppresses Hepatocellular Carcinoma Progression via PTPRS-STAT3 axis. Oncogene38, 7281–7293. 10.1038/s41388-019-0943-y
158
ZhangL.SunH.ZhaoF.LuP.GeC.LiH.et al (2012). BMP4 Administration Induces Differentiation of CD133+ Hepatic Cancer Stem Cells, Blocking Their Contributions to Hepatocellular Carcinoma. Cancer Res.72, 4276–4285. 10.1158/0008-5472.can-12-1013
159
ZhangT.DengL.XiongQ.SuS.GuJ. (2018). Anti-Müllerian Hormone Inhibits Proliferation and Induces Apoptosis in Epithelial Ovarian Cancer Cells by Regulating the Cell Cycle and Decreasing the Secretion of Stem Cell Factor. Oncol. Lett.16, 3260–3266. 10.3892/ol.2018.8985
160
ZhouY.LiuY.ZhangJ.YuD.LiA.SongH.et al (2020). Autocrine BMP4 Signaling Enhances Tumor Aggressiveness via Promoting Wnt/β-Catenin Signaling in IDH1-Mutant Gliomas. Transl. Oncol.13, 125–134. 10.1016/j.tranon.2019.10.019
Summary
Keywords
BMPs, ALKs, Smads, cancer, metastasis, angiogeneis
Citation
Ehata S and Miyazono K (2022) Bone Morphogenetic Protein Signaling in Cancer; Some Topics in the Recent 10 Years. Front. Cell Dev. Biol. 10:883523. doi: 10.3389/fcell.2022.883523
Received
25 February 2022
Accepted
09 May 2022
Published
25 May 2022
Volume
10 - 2022
Edited by
Long Zhang, Zhejiang University, China
Reviewed by
Blanca Herrera González, Complutense University of Madrid, Spain
Yabing Mu, Umeå University, Sweden
Updates
Copyright
© 2022 Ehata and Miyazono.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Shogo Ehata, ehata@wakayama-med.ac.jp
This article was submitted to Signaling, a section of the journal Frontiers in Cell and Developmental Biology
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.