Abstract
To date, immune checkpoint inhibitors have been successively approved and widely used in clinical cancer treatments, however, the overall response rates are very low and almost all cancer patients eventually progressed to drug resistance, this is mainly due to the intricate tumor microenvironment and immune escape mechanisms of cancer cells. One of the main key mechanisms leading to the evasion of immune attack is the presence of the immunosuppressive microenvironment within tumors. Recently, several studies illustrated that triggering receptor expressed on myeloid cells-2 (TREM2), a transmembrane receptor of the immunoglobulin superfamily, was a crucial pathology-induced immune signaling hub, and it played a vital negative role in antitumor immunity, such as inhibiting the proliferation of T cells. Here, we reviewed the recent advances in the study of TREM2, especially focused on its regulation of tumor-related immune signaling pathways and its role as a novel target in cancer immunotherapy.
Introduction
According to the latest cancer statistics, about 1.9 million new cancer cases and more than 600,000 cancer deaths are projected to occur in the United States in 2021 (), suggesting that malignant tumor is still a major public health problem worldwide. Over the past decade, tumor patients, especially those with advanced cancers witnessed the mushroom growth of cancer immunotherapies including oncolytic viruses, chimeric antigen receptor T cells, tumor vaccine and immune checkpoint inhibitors (ICIs) (, ), among them, ICIs were well on their way to becoming the most promising cancer treatment strategy. To a certain extent, the formerly embarrassing and intractable pattern of cancer therapy has been changed through the use of ICIs, hence Ipilimumab (Yervoy), the first anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) monoclonal antibody (mAb) and Pembrolizumab (Keytruda), the first mAb against programmed death-1 (PD-1) garnered their first global approvals for cancer treatment by United States Food and Drug Administration (FDA) in 2011 and 2014, respectively (, ). Soon afterwards, anti-programmed death-ligand1 (PD-L1) mAbs including Atezolizumab (Tecentriq) (), Avelumab (Bavencio) () and Durvalumab (Imfinzi) () were successively approved to be used in clinical cancer treatments. These ICIs have remarkably improved the outcomes of some malignancy types, for example, the use of ICIs increased the five-year survival rate of patients with advanced non-small cell lung cancer from 5% to 16%-25% (). In addition to the above three common ICIs, several novel immune checkpoint targets such as lymphocyte activation gene 3 (LAG3) (), T cell immunoglobulin and mucin domain 3 (TIM3) (), T cell immunoglobulin and ITIM domain (TIGIT) (), V-Domain Immunoglobulin-Containing Suppressor of T Cell Activation (VISTA) () and B7-H3 (also known as CD276) () were gradually discovered and recognized in recent years, some of them are undergoing clinical trials. However, the overall response rates of ICIs are very low and almost all cancer patients eventually progressed to drug resistance even though the combination therapies (for instance, combining two ICIs (, ), adding ICI to chemotherapy () or radiotherapy () or antiangiogenic therapy () were applied to improve the tricky prognosis, this was mainly due to the intricate tumor microenvironment (TME) and complicated immune escape mechanisms of cancer cells.
An increasing number of studies demonstrate that cancer immune evasion is one of the main obstacles in developing satisfactory anticancer therapeutic strategies, and the two key mechanisms leading to the evasion of immune attack are the abnormal expression and activation of immune checkpoints and the excessive formation of suppressive immune microenvironment within tumors (–). Hence, inhibition of immune checkpoints alone may not be sufficient to achieve desirable antitumor therapeutic effects, but removing the immunosuppressive microenvironment from tumors probable has a great chance to improve the prognosis of cancer patients and can be used in conjunction with ICIs. In recent years, researchers illustrated that triggering receptor expressed on myeloid cells-2 (TREM2), a transmembrane receptor of the immunoglobulin superfamily, was a crucial pathology-induced immune signaling hub, and more and more evidence suggested that TREM2 played a vital role in tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs). In this study, we first review the structure of TREM2 and the pathway of TREM2 signaling, then we focus on the role and potential of the tumor suppressor TREM2 in the regulation of tumor immune system and cancer immunotherapy.
TREM2 and TREM2 Signaling Pathway
Structure of TREM2
TREMs, which were identified as the new activating receptors of immunoglobulin superfamily expressed on human myeloid cells in 2000, include inhibitory and activating isoforms encoded by a gene cluster linked to the major histocompatibility complex (, ). Currently, studies had explored several members of TREM family proteins including TREM1 (also known as CD354), TREM2, TREM3, TREM4, plasmacytoid dendritic cell (pDC)-TREM, TREM-like transcript (TLT-1) and TLT-2, among them, TREM2 was an immunosuppressive receptor (), and it has successfully attracted the attention of oncologists in recent years.
TREM2 gene, which is located on human chromosome 6p21 with a total length of 4676 base pairs (), consists of five exons and encodes the glycoprotein TREM2 contains 230 amino acids (a.a.) (Figure 1) (). As a member of single transmembrane hyper-immunoglobulin family, TREM2 was initially cloned as a novel cDNA encoding a TREM1 homologue in 2000 (). Studies have shown that TREM2 is expressed in some myeloid cells including DCs, monocytes, osteoclasts, Kuppfer cells, alveolar macrophages and microglia (–), and its structure is consisted of the following four regions (Figure 1) (, ) (1): a signal peptide sequence (1~18 a.a.) (2); an extracellular domain (19~173 a.a.): contains an extracellular V-type immunoglobulin domain sequence followed by a short stalk sequence (3); a single transmembrane helix (174~195 a.a.): contains a charged lysine residue (3); a short cytoplasmic tail (196~230 a.a.): lacks signaling motifs.
Figure 1
In addition, TREM2 can be cleaved by sheddases of the metalloprotease family such as a disintegrin and metalloproteases 10 (ADAM10) and ADAM17, and then released as soluble TREM2 (sTREM2) (Figure 1) (, ). Schlepckow et al. found that both ADAM10 and ADAM17 cleaved TREM2 at histidine 157~serine 158 (, ). After being cleaved by ADAMs, the resultant transmembrane segment undergoes further proteolytic cleavage by γ-secretase (). However, whether TREM2 could be cleaved by other proteases is unknown now. Of greater significance, several studies had detected sTREM2 in the biological fluids (for example, cerebrospinal fluid) of patients suffering from Nasu-Hakola disease, multiple sclerosis and other inflammatory neurological diseases, and the level of sTREM2 was significantly related to disease severity (, ), indicating that sTREM2 would not only have a biological function but also a biomarker value.
TREM2 Signaling Pathway
To dates, studies have shown that TREM2 has several biological functions, including but not limited to cell maturation, cell proliferation, cell survival, phagocytosis and the regulation of inflammation (–). This diverse set of functions are mainly regulated by the interaction of TREM2 and a variety of potential TREM2 ligands, which encompass a wide array of anionic molecules including Gram-positive and Gram-negative bacteria (for example, Neisseria gonorrhoeae Escherichia coli and Staphylococcus aureus), DNA, lipoproteins and phospholipids (–). Some ligands such as low-density lipoprotein (LDL) and apolipoproteins E (Apo E) are physiologically present in the body, while some ligands including pathological β-amyloid oligomers (Aβ) are released as a consequence of tissue damage and cell death ().
Once TREM2 ligands bind to TREM2, TREM2 will interact with the adaptor proteins DNAX activation protein 12 (DAP12, also known as TYRO protein tyrosine kinase-binding protein) and DAP10 via oppositely charged residues, and then the TREM2-DAP12/DAP10 heterodimers are formed (, ), for example, the association of TREM2 to DAP12 is induced through a conserved positively-charged lysine in TREM2 (a.a.186) interacts with a negatively-charged aspartic acid residue in DAP12, thus resulting in the tyrosine phosphorylation of DAP12 within its immunoreceptor tyrosine-based activation motifs (ITAMs) by Src tyrosine kinases (, ) (Figure 2). The main kinase recruited by the ITAM region of DAP12 is spleen tyrosine kinase (SYK), which activates downstream signaling molecules such as phosphatidylinositol 3-kinase (PI3K), serine/threonine protein kinase Akt, mammalian target of rapamycin (mTOR), p38 mitogen-activated protein kinase (MAPK), extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK), ultimately leading to cell activation, cell survival and the increase level of intracellular calcium (–) (Figure 2). Moreover, TREM2-DAP10 also promotes signal transmission by recruiting PI3K and activating Akt and ERK (, ). Furthermore, Zheng et al. discovered that TREM2 could stabilize β-catenin by inhibiting its degradation via the Akt/GSK3β signaling pathway ().
Figure 2
Beyond the above signaling pathway, TREM2 also negatively regulates toll-like receptor (TLR) signaling pathways which play crucial roles in the innate immune system by recognizing pathogen-associated molecular patterns (). Long et al. found that TREM2 could attenuate Aβ1−42−mediated neuroinfammation through downregulating TLR signaling pathway (). The results of Zhou et al.’s study suggested that lipopolysaccharide (LPS)-induced hyperactive TLR4 might inhibit the negative effect of TREM2 on regulating inflammation, and the imbalance of microglial TLR4/TREM2 might be a potential link between Alzheimer’s disease and systemic inflammation (58). Moreover, the TREM2/TLR4/nuclear factor-kappa B (NF-κB) signaling pathway was illustrated had the function of inhibiting LPS-induced neuroinflammation by regulating microglial M1/M2 polarization (59).
TREM2: An Emerging Therapeutic Target of Cancer Immunotherapy
TREM2 Acts As a Tumor Suppressor in Cancer Environment
Researches over the past two decades have illustrated that the immune system could not only inhibit the growth of malignant tumors by destroying cancer cells but also promote the progression of malignancies either by selecting for cancer cells those are better suitable to survive in a host with a strong immune system or by establishing favorable condition within TME that facilitate the proliferation, growth, invasion and metastasis of tumors, this means the immune system has a “double-edged sword” effect on the development of cancers (60).
In order to be fit for cancer cell survival, tumors would coopt myeloid cells, which constitute an important cellular fraction of TME, to suppress the immune system through various mechanisms and then negatively regulate anti-tumor immune function (61, 62). It’s worth noting that recent studies have demonstrated that tumor-infiltrating myeloid cells are heterogeneous and may actually contain both immunostimulatory subpopulation and immunosuppressive subpopulation (63, 64), and MDSCs which can be subdivided as macrophages, granulocytes (especially neutrophils but occasionally and less numerous basophils and mast cells), monocytes and DCs are a immunosuppressive myeloid cell population characterized by the function of promoting tumor growth in tumor immune network (63, 65), this subpopulation also has been reported in relation to the resistance to immunotherapy such as ICIs (66). As some studies revealed, MDSCs possess high levels of arginase I (Arg1) which can induce T-cell anergy by depleting L-arginine, and thus impair T-cell proliferation and cytokine production and inhibit the expression of T-cell receptor CD3ζ chain and antigen-specific T-cell responses (67–69). In addition, the activation of MDSCs lead to the upregulated expression of inducible nitric oxide synthase and the increased production of nitric oxide and reactive oxygen species, and then result in the suppression of antitumor immunoactivity (61). Importantly, MDSCs also obtained the ability of promoting the development and induction of regulatory T (Treg) cells (70, 71). On the other hand, according to several high-dimensional profiling studies, immunostimulatory myeloid cells mainly include type I DCs and M1-like interferon (IFN)-γ-induced macrophages (63, 72, 73), and exert pro-inflammatory and antineoplastic functions through secreting some inflammatory factors (74). Therefore, it is strongly necessary to distinguish immunostimulatory myeloid cells and immunosuppressive myeloid cells, thus helping to deplete immunosuppressive myeloid cells from tumors and induce those cells with immunostimulatory properties to improve the therapeutic effect of anti-cancer immunotherapy strategies.
Previously, studies had demonstrated that TREM2 acted as a negative regulator of TLR responses in DCs and macrophages (75, 76). TREM2-deficient bone marrow-derived DCs (BMDCs) produced increased type I IFN (IFN-α4 and IFN-β) and inflammatory cytokines including IL-12, IL-6 and tumor necrosis factor (TNF) in response to TLR ligation, furthermore, compared with wild-type BMDCs, TREM2-deficient BMDCs were more efficient at inducing antigen-specific T cell proliferation upon CpG DNA stimulation (76), and Yao et al. got the similar result, they found that TREM2+ DCs performed a more potent inhibitory effect on the proliferation of T cells than TREM2- DCs (77) (Figure 3). In addition to these, Zhai et al. found that TREM2 had a modulatory effect on the phenotypic conversion of microglia, down-regulation of TREM2 could promote the phenotypic conversion of microglia to M1 phenotype, which induced the secretion of TNF-α, IL-1β and IL-6 and decreased IL-10 and transforming growth factor (TGF)-β (78) (Figure 3). Moreover, Wang and his colleagues illustrated that down-regulation of TREM2 significantly decreased the expression of chemokine ligand-10 (CXCL10), chemokine receptor-3 (CXCR3), matrix metalloproteinase-2 (MMP-2) and MMP-9 which played crucial roles in TME (79) (Figure 3). These results implied that TREM2 might play a similar role in antitumor immunity. In 2016, Yao et al. elucidated that, compared with normal control, TREM2 was dramatically overexpressed on peripheral blood monocytes and TAMs of patients with lung cancer and tumor-bearing mice, and there was a positive correlation between the level of TREM2 on pulmonary macrophages and the pathological staging or lymph nodes metastasis of lung cancer, the reduction of tumor burden by surgery or chemotherapy induced the remarkable decrease of TREM2 on the peripheral blood monocytes of lung cancer patients (77). In 2020, the research team of Colonna M used single-cell RNA sequencing (scRNA-seq) to dig deep into the tumor-suppressor myeloid cells, they innovatively discovered that TREM2 deficiency and anti-TREM2 mAb treatment could trigger remarkable changes in the macrophage populations infiltrating the tumor, the infiltration of immunosuppresssive macrophages labeled by MRC1 and CX3CR1 was reduced, while the novel subsets expressing immunostimulatory molecules were expanded, moreover, TREM2–/– tumor infiltrates contained more CD8+ T cells and CD4+ T cells which expressed PD-1 than wild-type infiltrates, suggesting that TREM2 deficiency might significantly promote the activation of T cells and potentially improve the responsiveness of cancers to anti-PD-1 mAbs (73) (Figure 3). Then, the authors revealed that TREM2 deficiency could modify the TME in a manner that facilitated partial control the growth of tumor by CD8+ T cells (73). At the same time, Amit I’s research team and Weiner A’s research team co-published the parallel excellent and surprising finding, they utilized INs-seq, a new technology for recording scRNA-seq and intracellular protein activity, uncovered a novel Arg1+ TREM2+ myeloid cells, genetic ablation of TREM2 could significantly inhibit the accumulation of myeloid cells within tumors and lead to immune reactivation (80).
Figure 3
In a word, more and more evidence indicate that TREM2 acts as a tumor suppressor in modulating TME, and the purposeful and accurate regulation of TREM2 signaling pathway has the potential to reshape the TME and exert a stronger anti-tumor effect.
Emerging and Novel Roles of TREM2 in Cancer Treatment
Up to now, the role of TREM2 in the treatments of malignant tumors is poorly understood, because relevant studies are relatively few, and most of the results are published in recent years. Initially, Wang et al. found that, compared with noncancerous brain tissues, the expression level of TREM2 was significantly increase in glioma tissues, and the overexpression of TREM2 in human gliomas was closely associated with pathological grade and overall survival of patients, furthermore, silencing TREM2 could inhibit the proliferation, migration and invasion of glioma cells (79). Before long, Zhang et al. demonstrated that TREM2 was abnormally upregulated in renal cell cancer tissues, knockdown of TREM2 significantly inhibited the progression of renal cell cancer via inactivating PI3K/Akt signaling pathway and increasing the expression of PTEN (81). In 2018, Zhang et al. confirmed that the mRNA and protein expression levels of TREM2 in gastric cancer tissues were significantly higher than those in normal gastric tissues, and the expression level of TREM2 was inversely correlated with the prognosis of patients with gastric cancer (82). In addition, by using a druggable genome small interfering RNA screening library, Duggan et al. found that targeting TREM2 triggered the cell death and reduced tumor burden of esophageal adenocarcinoma (83). These results indicated that TREM2 might be an excellent and effective therapeutic target for cancer treatment.
However, the study of Kim et al. suggested that TREM2 might also acted as a tumor suppressor in some human malignancies, because they detected that TREM2 significantly inhibited the proliferation of colon cancer cells by retarding cell cycle progression and suppressed the tumorigenicity of colon cancer cells through reducing the mRNA expression of pro-tumor cytokines (IL-4) and increasing the mRNA expression of anti-tumor cytokines (IL-12 and IL-15) (84). Importantly, compared with normal colon tissues and human colon carcinoma tissues with stage I, the colon carcinoma tissues with stage II, III and IV expressed lower level of TREM2 protein and this decrease was in a tumor stage-dependent manner (84). More interestingly, even though the expression level of TREM2 was upregulated in human hepatocellular carcinoma tissues, after administrating carcinogen diethylnitrosamine, TREM2-/- mice developed more liver tumors and displayed more deteriorative liver damage, inflammation, oxidative stress and hepatocyte proliferation, and then Esparza-Baquer et al. found that TREM2 played a protective role in the biological process of hepatocarcinogenesis via different pleiotropic effects (85). Recently, Wang et al. revealed a novel role of TREM2 in mediating chemoresistance, they found that TREM2 was a potential target of microRNA-149 in gastric cancer, the overexpression of microRNA-149 could decrease the expression of TREM2 and further improve the 5-fluorouracil resistance through β-catenin signaling pathway (86). The above studies show that TREM2 plays different and even opposite roles in the pathogenesis, development and progression of different kind of malignant tumors, and its specific biological functions still need to be further confirmed by a large number of studies.
Application of TREM2 in Cancer Immunotherapy
Now, a lot of outstanding cancer immunotherapy drugs, especially ICIs, have been successfully transformed from the laboratory to the clinical application, the update and summary on ICIs approved by the FDA is shown in Table 1 (, 87, 88). Although ICIs have great promise, only a small population of cancer patients achieve a lasting response to the monotherapy (88). With the use of some predictive biomarkers such as PD-L1 to identify those patients who are more likely to acquire a favorable therapeutic effect from exposure to ICIs, the overall effect of cancer immunotherapy has been improved to a certain extent, but there is still a lot of room for improvement.
Table 1
| Immune checkpoints | ICIs | Cancer types or tissue-agnostic conditions (first approved time, year) |
|---|---|---|
| PD-1 | Pembrolizumab (Keytruda) | (1) Melanoma (2014); (2) Non-small cell lung cancer (2015); (3) Head and neck squamous cell carcinoma (2016); (4) Urothelial carcinoma (2017); (5) Classical Hodgkin’s lymphoma (2017); (6) Gastric cancer (2017); (7) Solid tumor with microsatellite instability (MSI-H) or mismatch repair-deficient (dMMR) status (2017); (8) Cervical cancer (2018); (9) Hepatocellular carcinoma (2018); (10) Merkel cell carcinoma (2018); (11) Primary mediastinal large B cell lymphoma (2018); (12) Renal cell cancer (2019); (13) Small cell lung cancer (2019); (14) Esophageal squamous cell carcinoma (2019); (15) Endometrial carcinoma (2019); (16) Bacillus Calmette-Guérin bladder cancer (2020); (17) Colorectal cancer (2020); (18) Cutaneous squamous cell carcinoma (2020); (19) Triple-negative breast cancer (2020); (20) Tumor mutational burden high cancer as determined by an FDA approved test (2020). |
| PD-1 | Nivolumab (Opdivo) | (1) Melanoma (2014); (2) Non-small cell lung cancer (2015); (3) Renal cell cancer (2015); (4) Head and neck squamous cell carcinoma (2016); (5) Classical Hodgkin’s lymphoma (2016); (6) Urothelial carcinoma (2017); (7) Solid tumor with MSI-H or dMMR status (2017); (8) Hepatocellular carcinoma (2017); (9) Small cell lung cancer (2018); (10) Esophageal squamous cell carcinoma (2020); (11) Pleural mesothelioma (2020). |
| Cemiplimab (Libtayo) | Cutaneous squamous cell carcinoma (2018). | |
| PD-L1 | Atezolizumab (Tecentriq) | (1) Non-small cell lung cancer (2016); (2) Urothelial carcinoma (2016); (3) Small cell lung cancer (2019); (4) Triple-negative breast cancer (2019); (5) Melanoma (2020); (6) Hepatocellular carcinoma (2020). |
| PD-L1 | Durvalumab (Imfinzi) | (1) Urothelial carcinoma (2017); (2) Non-small cell lung cancer (2018); (3) Small cell lung cancer (2020). |
| Avelumab (Bavencio). | (1) Urothelial carcinoma (2017); (2) Merkel cell carcinoma (2017); (3) Renal cell cancer (2019). | |
| CTLA-4 | Ipilimumab (Yervoy) | Melanoma (2011). |
| Tremelimumab | Malignant mesothelioma (2015). |
Update and summary of ICIs approved by FDA for cancer treatments.
In terms of TREM2, the above content has implied that it plays a vital role in immune responses to tumors and is emerging as a novel immunotherapy target. Molgora et al. found that constitutive lack of TREM2 or anti-TREM2 mAb significantly curbed the growth of tumors and led to complete tumor regression when associated with suboptimal PD-1 immunotherapy (73), the encouraging results indicate that therapeutic strategies targeting TREM2 could keep pace with ICIs in cancer immunotherapy. In addition, Xiong et al. re-analyzed a publicly available scRNA-seq dataset of melanoma samples of patients subjected to ICIs and identified a subpopulation of macrophages overexpressing TREM2 that were overrepresented in the non-responding tumors, and this subpopulation of macrophages might contribute to the resistance of ICIs (89). In order to systematically explore the potential immunological functions and the potential prognostic value of TREM2 across 33 cancer types, Cheng et al. conducted a pan-cancer analysis based on datasets from The Cancer Genome Atlas, the Cancer Cell Line Encyclopedia, Genotype Tissue-Expression, cBioPortal and Human Protein Atlas, they used the ESTIMATE algorithm to calculate the immune scores across the 33 types of cancers, their results showed that the expression level of TREM2 was significantly positively correlated with immune scores in diffuse large B-cell lymphoma, acute myeloid leukemia and thymoma, and the levels of immune cell infiltration were significantly correlated with TREM2 expression in most types of malignancies (90), this indicated that TREM2 could function as a prognostic marker in various cancers because of its especial role in tumorigenesis and tumor immunity. Lately, Lee et al. demonstrated for the first time that precursor natural killer (pNK) cells expressed TREM2, compared with wild type mice, the population of pNK cells and the expression levels of NK cell-activating receptors and NK cell-associated genes were all increased in TREM2-overexpressing transgenic mice, on the contrary, the inhibition of TREM2 signaling pathway by TREM2-immunoglobulin or PI3K inhibitor impacted the expression of NK cell receptor repertoire and downregulated the expression levels of NK cell-associated genes, thus significantly impaired the differentiation of NK cells, the results of this study collectively suggested again that TREM2 might act as a novel candidate for cancer immunotherapy (91).
Because of the outstanding function in regulating the immune system, there is currently a clinical trial investigating the effect of a drug named PY314 which targets TREM2 in the treatment of solid malignancies (Clinical Trials No.: NCT04691375), it is a phase 1a/1b open-label study aims to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of PY314 as a single agent and in combination with Pembrolizumab in subjects with advanced solid tumors, the drug PY314 was designed to selectively consume immunosuppressive cells and promote the rebalance of TME that facilitates anti-tumor immunity, we expect that satisfactory results would be obtained from this clinical study, and thus further promotes the clinical transformation and application of therapeutic strategies targeting TREM2.
Even though few clinical studies about targeting TREM2 in cancer treatment are conducting now, the potential for clinical translation of TREM2-targeted therapies remains high in the future, and numerous possible interventions are existed to tackle the TREM2 and its signaling pathway (). The most prominent and direct intervention is to deplete TREM2 genes or target the active domain of TREM2 through using a specific mAb or small molecule which would block the downstream pathways (73). Another potential approach is to target TREM2 ligands, especially condition-specific and/or tissue-specific ligands, but relevant studies is rare now (). Furthermore, TREM2 is shed by the ADAMs, so the inhibition of the cleaved process is possible to become another feasible intervention (92), but it is noteworthy that the incidence rate of unwanted and inevitable side effects may be high, because ADAM10 and ADAM17 have a wide range of substrates such as junction molecules, adhesion molecules and chemokines and cytokines (93). In order to selectively compete for α-secretase-mediated shedding, Schlepckow et al. identified a mAb named 4D9, which had a stalk region epitope close to the cleavage site, not only stabilized TREM2 on the surface of cells and reducing its proteolytic shedding by ADAMs, but also concomitantly activated the phosphorylation of SYK (94). Finally, the inhibition of the specific intracellular signaling cascade downstream molecules of TREM2 is another different strategy, however, as we all know, DAP12, DAP10, SYK, PI3K, Akt, mTOR and MAPK are also involved in lots of other signal transduction pathways, hence targeting the above molecules may be an ineffective therapeutic method in the context of TREM2-specific treatment.
In conclusion, a growing body of evidence suggests that TREM2 acts as a key signaling hub in tumorigenesis, tumor progression and oncotherapy, and TREM2 may play different or even opposite roles in different malignancies. Therefore, there is still a long and difficult road ahead to explore the exact roles of TREM2 in each malignancy type with different pathologic category and histological origin. More importantly, because TREM2 has been demonstrated by some basic research as an excellent and effective therapeutic target for cancer immunotherapy, more clinical studies or clinical trials are urgently needed to confirm its roles in the treatment of cancer, and promoted the clinical transformation of TREM2 as soon as possible so as to benefit more cancer patients.
Funding
This research was funded by National Natural Science Foundation of China, grant number 81972845; Introduction of Specialist Team in Clinical Medicine of Xuzhou, grant number 2019TD003; Graduate Research and Practice Innovation Plan of Jiangsu Province, grant number KYCX21_2660.
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.
Statements
Author contributions
Conceptualization, LZ and XD. Data curation, HQ, XW, JJ, and LH. Writing—original draft preparation, HQ, ZS, QM, and YW. Writing—review and editing, LZ, HQ, and ZS. Visualization, HQ and XW. Supervision, LZ and XD. All authors contributed to the article and approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
References
1
SiegelRLMillerKDFuchsHEJemalA. Cancer Statistics, 2021. CA Cancer J Clin (2021) 71(1):7–33. doi: 10.3322/caac.21654
2
MellmanICoukosGDranoffG. Cancer Immunotherapy Comes of Age. Nature (2011) 480(7378):480–9. doi: 10.1038/nature10673
3
FinckAGillSIJuneCH. Cancer Immunotherapy Comes of Age and Looks for Maturity. Nat Commun (2020) 11(1):3325. doi: 10.1038/s41467-020-17140-5
4
CameronFWhitesideGPerryC. Ipilimumab: First Global Approval. Drugs (2011) 71(8):1093–104. doi: 10.2165/11594010-000000000-00000
5
PooleRM. Pembrolizumab: First Global Approval. Drugs (2014) 74(16):1973–81. doi: 10.1007/s40265-014-0314-5
6
MarkhamA. Atezolizumab: First Global Approval. Drugs (2016) 76(12):1227–32. doi: 10.1007/s40265-016-0618-8
7
KimES. Avelumab: First Global Approval. Drugs (2017) 77(8):929–37. doi: 10.1007/s40265-017-0749-6
8
SyedYY. Durvalumab: First Global Approval. Drugs (2017) 77(12):1369–76. doi: 10.1007/s40265-017-0782-5
9
FriedlaenderAAddeoABannaG. New Emerging Targets in Cancer Immunotherapy: The Role of TIM3. ESMO Open (2019) 4(Suppl 3):e000497. doi: 10.1136/esmoopen-2019-000497
10
RuffoEWuRCBrunoTCWorkmanCJVignaliDAA. Lymphocyte-Activation Gene 3 (LAG3): The Next Immune Checkpoint Receptor. Semin Immunol (2019) 42:101305. doi: 10.1016/j.smim.2019.101305
11
HarjunpaaHGuillereyC. TIGIT as an Emerging Immune Checkpoint. Clin Exp Immunol (2020) 200(2):108–19. doi: 10.1111/cei.13407
12
TagliamentoMBironzoPNovelloS. New Emerging Targets in Cancer Immunotherapy: The Role of VISTA. ESMO Open (2020) 4(Suppl 3):e000683. doi: 10.1136/esmoopen-2020-000683
13
YangSWeiWZhaoQ. B7-H3, A Checkpoint Molecule, as a Target for Cancer Immunotherapy. Int J Biol Sci (2020) 16(11):1767–73. doi: 10.7150/ijbs.41105
14
HellmannMDCiuleanuTEPluzanskiALeeJSOttersonGAAudigier-ValetteCet al. Nivolumab Plus Ipilimumab in Lung Cancer With a High Tumor Mutational Burden. N Engl J Med (2018) 378(22):2093–104. doi: 10.1056/NEJMoa1801946
15
MotzerRJTannirNMMcDermottDFAren FronteraOMelicharBChoueiriTKet al. Nivolumab Plus Ipilimumab Versus Sunitinib in Advanced Renal-Cell Carcinoma. N Engl J Med (2018) 378(14):1277–90. doi: 10.1056/NEJMoa1712126
16
GandhiLRodriguez-AbreuDGadgeelSEstebanEFelipEDe AngelisFet al. Pembrolizumab Plus Chemotherapy in Metastatic Non-Small-Cell Lung Cancer. N Engl J Med (2018) 378(22):2078–92. doi: 10.1056/NEJMoa1801005
17
BahigHAubinFStaggJGologanOBallivyOBissadaEet al. Phase I/II Trial of Durvalumab Plus Tremelimumab and Stereotactic Body Radiotherapy for Metastatic Head and Neck Carcinoma. BMC Cancer (2019) 19(1):68. doi: 10.1186/s12885-019-5266-4
18
DudekAZLiuLCGuptaSLoganTFSingerEAJoshiMet al. Phase Ib/II Clinical Trial of Pembrolizumab With Bevacizumab for Metastatic Renal Cell Carcinoma: BTCRC-GU14-003. J Clin Oncol (2020) 38(11):1138–45. doi: 10.1200/JCO.19.02394
19
VinayDSRyanEPPawelecGTalibWHStaggJElkordEet al. Immune Evasion in Cancer: Mechanistic Basis and Therapeutic Strategies. Semin Cancer Biol (2015) 35 Suppl:S185–98. doi: 10.1016/j.semcancer.2015.03.004
20
AlsaabHOSauSAlzhraniRTatipartiKBhiseKKashawSKet al. PD-1 and PD-L1 Checkpoint Signaling Inhibition for Cancer Immunotherapy: Mechanism, Combinations, and Clinical Outcome. Front Pharmacol (2017) 8:561. doi: 10.3389/fphar.2017.00561
21
De CiccoPErcolanoGIanaroA. The New Era of Cancer Immunotherapy: Targeting Myeloid-Derived Suppressor Cells to Overcome Immune Evasion. Front Immunol (2020) 11:1680. doi: 10.3389/fimmu.2020.01680
22
BouchonADietrichJColonnaM. Cutting Edge: Inflammatory Responses Can Be Triggered by TREM-1, A Novel Receptor Expressed on Neutrophils and Monocytes. J Immunol (2000) 164(10):4991–5. doi: 10.4049/jimmunol.164.10.4991
23
ColonnaM. TREMs in the Immune System and Beyond. Nat Rev Immunol (2003) 3(6):445–53. doi: 10.1038/nri1106
24
PelhamCJPandyaANAgrawalDK. Triggering Receptor Expressed on Myeloid Cells Receptor Family Modulators: A Patent Review. Expert Opin Ther Pat (2014) 24(12):1383–95. doi: 10.1517/13543776.2014.977865
25
AllcockRJBarrowADForbesSBeckSTrowsdaleJ. The Human TREM Gene Cluster at 6p21.1 Encodes Both Activating and Inhibitory Single IgV Domain Receptors and Includes Nkp44. Eur J Immunol (2003) 33(2):567–77. doi: 10.1002/immu.200310033
26
BouchonAHernandez-MunainCCellaMColonnaM. A DAP12-Mediated Pathway Regulates Expression of CC Chemokine Receptor 7 and Maturation of Human Dendritic Cells. J Exp Med (2001) 194(8):1111–22. doi: 10.1084/jem.194.8.1111
27
HumphreyMBDawsMRSpustaSCNiemiECTorchiaJALanierLLet al. TREM2, A DAP12-Associated Receptor, Regulates Osteoclast Differentiation and Function. J Bone Miner Res (2006) 21(2):237–45. doi: 10.1359/JBMR.051016
28
NeumannHTakahashiK. Essential Role of the Microglial Triggering Receptor Expressed on Myeloid Cells-2 (TREM2) for Central Nervous Tissue Immune Homeostasis. J Neuroimmunol (2007) 184(1-2):92–9. doi: 10.1016/j.jneuroim.2006.11.032
29
KothLLCambierCJEllwangerASolonMHouLLanierLLet al. DAP12 is Required for Macrophage Recruitment to the Lung in Response to Cigarette Smoke and Chemotaxis Toward CCL2. J Immunol (2010) 184(11):6522–8. doi: 10.4049/jimmunol.0901171
30
ForaboscoPRamasamyATrabzuniDWalkerRSmithCBrasJet al. Insights Into TREM2 Biology by Network Analysis of Human Brain Gene Expression Data. Neurobiol Aging (2013) 34(12):2699–714. doi: 10.1016/j.neurobiolaging.2013.05.001
31
GoncalvesLARodrigues-DuarteLRodoJVieira de MoraesLMarquesIPenha-GoncalvesC. TREM2 Governs Kupffer Cell Activation and Explains Belr1 Genetic Resistance to Malaria Liver Stage Infection. Proc Natl Acad Sci USA (2013) 110(48):19531–6. doi: 10.1073/pnas.1306873110
32
HuNTanMSYuJTSunLTanLWangYLet al. Increased Expression of TREM2 in Peripheral Blood of Alzheimer's Disease Patients. J Alzheimers Dis (2014) 38(3):497–501. doi: 10.3233/JAD-130854
33
LiJTZhangY. TREM2 Regulates Innate Immunity in Alzheimer's Disease. J Neuroinflamm (2018) 15(1):107. doi: 10.1186/s12974-018-1148-y
34
YangJFuZZhangXXiongMMengLZhangZ. TREM2 Ectodomain and Its Soluble Form in Alzheimer's Disease. J Neuroinflamm (2020) 17(1):204. doi: 10.1186/s12974-020-01878-2
35
WunderlichPGlebovKKemmerlingNTienNTNeumannHWalterJ. Sequential Proteolytic Processing of the Triggering Receptor Expressed on Myeloid Cells-2 (TREM2) Protein by Ectodomain Shedding and Gamma-Secretase-Dependent Intramembranous Cleavage. J Biol Chem (2013) 288(46):33027–36. doi: 10.1074/jbc.M113.517540
36
LichtenthalerSFLembergMKFluhrerR. Proteolytic Ectodomain Shedding of Membrane Proteins in Mammals-Hardware, Concepts, and Recent Developments. EMBO J (2018) 37(15):e99456. doi: 10.15252/embj.201899456
37
FeuerbachDSchindlerPBarskeCJollerSBeng-LoukaEWorringerKAet al. ADAM17 Is the Main Sheddase for the Generation of Human Triggering Receptor Expressed in Myeloid Cells (Htrem2) Ectodomain and Cleaves TREM2 After Histidine 157. Neurosci Lett (2017) 660:109–14. doi: 10.1016/j.neulet.2017.09.034
38
SchlepckowKKleinbergerGFukumoriAFeederleRLichtenthalerSFSteinerHet al. An Alzheimer-Associated TREM2 Variant Occurs at the ADAM Cleavage Site and Affects Shedding and Phagocytic Function. EMBO Mol Med (2017) 9(10):1356–65. doi: 10.15252/emmm.201707672
39
PalonevaJManninenTChristmanGHovanesKMandelinJAdolfssonRet al. Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotype. Am J Hum Genet (2002) 71(3):656–62. doi: 10.1086/342259
40
PiccioLBuonsantiCCellaMTassiISchmidtREFenoglioCet al. Identification of Soluble TREM-2 in the Cerebrospinal Fluid and Its Association With Multiple Sclerosis and CNS Inflammation. Brain (2008) 131(Pt 11):3081–91. doi: 10.1093/brain/awn217
41
HsiehCLKoikeMSpustaSCNiemiECYenariMNakamuraMCet al. A Role for TREM2 Ligands in the Phagocytosis of Apoptotic Neuronal Cells by Microglia. J Neurochem (2009) 109(4):1144–56. doi: 10.1111/j.1471-4159.2009.06042.x
42
KawaboriMKacimiRKauppinenTCalosingCKimJYHsiehCLet al. Triggering Receptor Expressed on Myeloid Cells 2 (TREM2) Deficiency Attenuates Phagocytic Activities of Microglia and Exacerbates Ischemic Damage in Experimental Stroke. J Neurosci (2015) 35(8):3384–96. doi: 10.1523/JNEUROSCI.2620-14.2015
43
DeczkowskaAWeinerAAmitI. The Physiology, Pathology, and Potential Therapeutic Applications of the TREM2 Signaling Pathway. Cell (2020) 181(6):1207–17. doi: 10.1016/j.cell.2020.05.003
44
DawsMRSullamPMNiemiECChenTTTchaoNKSeamanWE. Pattern Recognition by TREM-2: Binding of Anionic Ligands. J Immunol (2003) 171(2):594–9. doi: 10.4049/jimmunol.171.2.594
45
QuanDNCooperMDPotterJLRobertsMHChengHJarvisGA. TREM-2 Binds to Lipooligosaccharides of Neisseria Gonorrhoeae and Is Expressed on Reproductive Tract Epithelial Cells. Mucosal Immunol (2008) 1(3):229–38. doi: 10.1038/mi.2008.1
46
KoberDLBrettTJ. TREM2-Ligand Interactions in Health and Disease. J Mol Biol (2017) 429(11):1607–29. doi: 10.1016/j.jmb.2017.04.004
47
PengQMalhotraSTorchiaJAKerrWGCoggeshallKMHumphreyMB. TREM2- and DAP12-Dependent Activation of PI3K Requires DAP10 and Is Inhibited by SHIP1. Sci Signal (2010) 3(122):ra38. doi: 10.1126/scisignal.2000500
48
CallMEWucherpfennigKWChouJJ. The Structural Basis for Intramembrane Assembly of an Activating Immunoreceptor Complex. Nat Immunol (2010) 11(11):1023–9. doi: 10.1038/ni.1943
49
GratuzeMLeynsCEGHoltzmanDM. New Insights Into the Role of TREM2 in Alzheimer's Disease. Mol Neurodegener (2018) 13(1):66. doi: 10.1186/s13024-018-0298-9
50
SadaKTakanoTYanagiSYamamuraH. Structure and Function of Syk Protein-Tyrosine Kinase. J Biochem (2001) 130(2):177–86. doi: 10.1093/oxfordjournals.jbchem.a002970
51
MocsaiARulandJTybulewiczVL. The SYK Tyrosine Kinase: A Crucial Player in Diverse Biological Functions. Nat Rev Immunol (2010) 10(6):387–402. doi: 10.1038/nri2765
52
SunMZhuMChenKNieXDengQHazlettLDet al. TREM-2 Promotes Host Resistance Against Pseudomonas Aeruginosa Infection by Suppressing Corneal Inflammation via a PI3K/Akt Signaling Pathway. Invest Ophthalmol Vis Sci (2013) 54(5):3451–62. doi: 10.1167/iovs.12-10938
53
UllandTKSongWMHuangSCUlrichJDSergushichevABeattyWLet al. TREM2 Maintains Microglial Metabolic Fitness in Alzheimer's Disease. Cell (2017) 170(4):649–63.e613. doi: 10.1016/j.cell.2017.07.023
54
ZhangJLiuYZhengYLuoYDuYZhaoYet al. TREM-2-P38 MAPK Signaling Regulates Neuroinflammation During Chronic Cerebral Hypoperfusion Combined With Diabetes Mellitus. J Neuroinflamm (2020) 17(1):2. doi: 10.1186/s12974-019-1688-9
55
ZhengHJiaLLiuCCRongZZhongLYangLet al. TREM2 Promotes Microglial Survival by Activating Wnt/beta-Catenin Pathway. J Neurosci (2017) 37(7):1772–84. doi: 10.1523/JNEUROSCI.2459-16.2017
56
KawasakiTKawaiT. Toll-Like Receptor Signaling Pathways. Front Immunol (2014) 5:461. doi: 10.3389/fimmu.2014.00461
57
LongHZhongGWangCZhangJZhangYLuoJet al. TREM2 Attenuates Abeta1-42-Mediated Neuroinflammation in BV-2 Cells by Downregulating TLR Signaling. Neurochem Res (2019) 44(8):1830–9. doi: 10.1007/s11064-019-02817-1
58
ZhouJYuWZhangMTianXLiYLuY. Imbalance of Microglial TLR4/TREM2 in LPS-Treated APP/PS1 Transgenic Mice: A Potential Link Between Alzheimer's Disease and Systemic Inflammation. Neurochem Res (2019) 44(5):1138–51. doi: 10.1007/s11064-019-02748-x
59
ZhangJZhengYLuoYDuYZhangXFuJ. Curcumin Inhibits LPS-Induced Neuroinflammation by Promoting Microglial M2 Polarization via TREM2/ TLR4/ NF-kappaB Pathways in BV2 Cells. Mol Immunol (2019) 116:29–37. doi: 10.1016/j.molimm.2019.09.020
60
SchreiberRDOldLJSmythMJ. Cancer Immunoediting: Integrating Immunity's Roles in Cancer Suppression and Promotion. Science (2011) 331(6024):1565–70. doi: 10.1126/science.1203486
61
GabrilovichDINagarajS. Myeloid-Derived Suppressor Cells as Regulators of the Immune System. Nat Rev Immunol (2009) 9(3):162–74. doi: 10.1038/nri2506
62
UckunFM. Overcoming the Immunosuppressive Tumor Microenvironment in Multiple Myeloma. Cancers (Basel) (2021) 13(9):2018. doi: 10.3390/cancers13092018
63
BrozMLKrummelMF. The Emerging Understanding of Myeloid Cells as Partners and Targets in Tumor Rejection. Cancer Immunol Res (2015) 3(4):313–9. doi: 10.1158/2326-6066.CIR-15-0041
64
GubinMMEsaulovaEWardJPMalkovaONRunciDWongPet al. High-Dimensional Analysis Delineates Myeloid and Lymphoid Compartment Remodeling During Successful Immune-Checkpoint Cancer Therapy. Cell (2018) 175(4):1014–30.e1019. doi: 10.1016/j.cell.2018.09.030
65
CaiJCuiYYangJWangS. Epithelial-Mesenchymal Transition: When Tumor Cells Meet Myeloid-Derived Suppressor Cells. Biochim Biophys Acta Rev Cancer (2021) 1876(1):188564. doi: 10.1016/j.bbcan.2021.188564
66
Olivares-HernandezAFiguero-PerezLTeran-BrageELopez-GutierrezAVelascoATSarmientoRGet al. Resistance to Immune Checkpoint Inhibitors Secondary to Myeloid-Derived Suppressor Cells: A New Therapeutic Targeting of Haematological Malignancies. J Clin Med (2021) 10(9):1919. doi: 10.3390/jcm10091919
67
SchmielauJFinnOJ. Activated Granulocytes and Granulocyte-Derived Hydrogen Peroxide Are the Underlying Mechanism of Suppression of T-Cell Function in Advanced Cancer Patients. Cancer Res (2001) 61(12):4756–60.
68
RodriguezPCQuicenoDGZabaletaJOrtizBZeaAHPiazueloMBet al. Arginase I Production in the Tumor Microenvironment by Mature Myeloid Cells Inhibits T-Cell Receptor Expression and Antigen-Specific T-Cell Responses. Cancer Res (2004) 64(16):5839–49. doi: 10.1158/0008-5472.CAN-04-0465
69
ZeaAHRodriguezPCAtkinsMBHernandezCSignorettiSZabaletaJet al. Arginase-Producing Myeloid Suppressor Cells in Renal Cell Carcinoma Patients: A Mechanism of Tumor Evasion. Cancer Res (2005) 65(8):3044–8. doi: 10.1158/0008-5472.CAN-04-4505
70
HuangBPanPYLiQSatoAILevyDEBrombergJet al. Gr-1+CD115+ Immature Myeloid Suppressor Cells Mediate the Development of Tumor-Induced T Regulatory Cells and T-Cell Anergy in Tumor-Bearing Host. Cancer Res (2006) 66(2):1123–31. doi: 10.1158/0008-5472.CAN-05-1299
71
YangRCaiZZhangYYutzyWHTRobyKFRodenRB. CD80 in Immune Suppression by Mouse Ovarian Carcinoma-Associated Gr-1+CD11b+ Myeloid Cells. Cancer Res (2006) 66(13):6807–15. doi: 10.1158/0008-5472.CAN-05-3755
72
CassettaLPollardJW. Targeting Macrophages: Therapeutic Approaches in Cancer. Nat Rev Drug Discov (2018) 17(12):887–904. doi: 10.1038/nrd.2018.169
73
MolgoraMEsaulovaEVermiWHouJChenYLuoJet al. TREM2 Modulation Remodels the Tumor Myeloid Landscape Enhancing Anti-PD-1 Immunotherapy. Cell (2020) 182(4):886–900 e817. doi: 10.1016/j.cell.2020.07.013
74
CuiJShanKYangQQiYQuHLiJet al. Prostaglandin E3 Attenuates Macrophage-Associated Inflammation and Prostate Tumour Growth by Modulating Polarization. J Cell Mol Med (2021) 25(12):5586–601. doi: 10.1111/jcmm.16570
75
HamermanJAJarjouraJRHumphreyMBNakamuraMCSeamanWELanierLL. Cutting Edge: Inhibition of TLR and FcR Responses in Macrophages by Triggering Receptor Expressed on Myeloid Cells (TREM)-2 and DAP12. J Immunol (2006) 177(4):2051–5. doi: 10.4049/jimmunol.177.4.2051
76
ItoHHamermanJA. TREM-2, Triggering Receptor Expressed on Myeloid Cell-2, Negatively Regulates TLR Responses in Dendritic Cells. Eur J Immunol (2012) 42(1):176–85. doi: 10.1002/eji.201141679
77
YaoYLiHChenJXuWYangGBaoZet al. TREM-2 Serves as a Negative Immune Regulator Through Syk Pathway in an IL-10 Dependent Manner in Lung Cancer. Oncotarget (2016) 7(20):29620–34. doi: 10.18632/oncotarget.8813
78
ZhaiQLiFChenXJiaJSunSZhouDet al. Triggering Receptor Expressed on Myeloid Cells 2, A Novel Regulator of Immunocyte Phenotypes, Confers Neuroprotection by Relieving Neuroinflammation. Anesthesiology (2017) 127(1):98–110. doi: 10.1097/ALN.0000000000001628
79
WangXQTaoBBLiBWangXHZhangWCWanLet al. Overexpression of TREM2 Enhances Glioma Cell Proliferation and Invasion: A Therapeutic Target in Human Glioma. Oncotarget (2016) 7(3):2354–66. doi: 10.18632/oncotarget.6221
80
KatzenelenbogenYShebanFYalinAYofeISvetlichnyyDJaitinDAet al. Coupled scRNA-Seq and Intracellular Protein Activity Reveal an Immunosuppressive Role of TREM2 in Cancer. Cell (2020) 182(4):872–85.e819. doi: 10.1016/j.cell.2020.06.032
81
ZhangHShengLTaoJChenRLiYSunZet al. Depletion of the Triggering Receptor Expressed on Myeloid Cells 2 Inhibits Progression of Renal Cell Carcinoma via Regulating Related Protein Expression and PTEN-PI3K/Akt Pathway. Int J Oncol (2016) 49(6):2498–506. doi: 10.3892/ijo.2016.3740
82
ZhangXWangWLiPWangXNiK. High TREM2 Expression Correlates With Poor Prognosis in Gastric Cancer. Hum Pathol (2018) 72:91–9. doi: 10.1016/j.humpath.2017.10.026
83
DugganSPGarryCBehanFMPhippsSKudoHKircaMet al. siRNA Library Screening Identifies a Druggable Immune-Signature Driving Esophageal Adenocarcinoma Cell Growth. Cell Mol Gastroenterol Hepatol (2018) 5(4):569–90. doi: 10.1016/j.jcmgh.2018.01.012
84
KimSMKimEMJiKYLeeHYYeeSMWooSMet al. TREM2 Acts as a Tumor Suppressor in Colorectal Carcinoma Through Wnt1/beta-Catenin and Erk Signaling. Cancers (Basel) (2019) 11(9):1315. doi: 10.3390/cancers11091315
85
Esparza-BaquerALabianoISharifOAgirre-LizasoAOakleyFRodriguesPMet al. TREM-2 Defends the Liver Against Hepatocellular Carcinoma Through Multifactorial Protective Mechanisms. Gut (2020) 70(7):1345–61. doi: 10.1136/gutjnl-2019-319227
86
WangXYZhouYCWangYLiuYYWangYXChenDDet al. miR-149 Contributes to Resistance of 5-FU in Gastric Cancer via Targeting TREM2 and Regulating Beta-Catenin Pathway. Biochem Biophys Res Commun (2020) 532(3):329–35. doi: 10.1016/j.bbrc.2020.05.135
87
GuazzelliAHussainMKrstic-DemonacosMMuttiL. Tremelimumab for the Treatment of Malignant Mesothelioma. Expert Opin Biol Ther (2015) 15(12):1819–29. doi: 10.1517/14712598.2015.1116515
88
TwomeyJDZhangB. Cancer Immunotherapy Update: FDA-Approved Checkpoint Inhibitors and Companion Diagnostics. AAPS J (2021) 23(2):39. doi: 10.1208/s12248-021-00574-0
89
XiongDWangYYouM. A Gene Expression Signature of TREM2(hi) Macrophages and Gammadelta T Cells Predicts Immunotherapy Response. Nat Commun (2020) 11(1):5084. doi: 10.1038/s41467-020-18546-x
90
ChengXWangXNieKChengLZhangZHuYet al. Systematic Pan-Cancer Analysis Identifies TREM2 as an Immunological and Prognostic Biomarker. Front Immunol (2021) 12:646523. doi: 10.3389/fimmu.2021.646523
91
LeeHYLeeEHYiJJiKYKimSMChoiHRet al. TREM2 Promotes Natural Killer Cell Development in CD3(-)CD122(+)NK1.1(+) pNK Cells. BMC Immunol (2021) 22(1):30. doi: 10.1186/s12865-021-00420-0
92
VoytyukIDe StrooperBChavez-GutierrezL. Modulation of Gamma- and Beta-Secretases as Early Prevention Against Alzheimer's Disease. Biol Psychiatry (2018) 83(4):320–7. doi: 10.1016/j.biopsych.2017.08.001
93
AljohmaniAYildizD. A Disintegrin and Metalloproteinase-Control Elements in Infectious Diseases. Front Cardiovasc Med (2020) 7:608281. doi: 10.3389/fcvm.2020.608281
94
SchlepckowKMonroeKMKleinbergerGCantuti-CastelvetriLParhizkarSXiaDet al. Enhancing Protective Microglial Activities With a Dual Function TREM2 Antibody to the Stalk Region. EMBO Mol Med (2020) 12(4):e11227. doi: 10.15252/emmm.201911227
Summary
Keywords
TREM2, immune checkpoint inhibitor, immunosuppressive myeloid cell, cancer immunotherapy, immune microenvironment
Citation
Qiu H, Shao Z, Wen X, Jiang J, Ma Q, Wang Y, Huang L, Ding X and Zhang L (2021) TREM2: Keeping Pace With Immune Checkpoint Inhibitors in Cancer Immunotherapy. Front. Immunol. 12:716710. doi: 10.3389/fimmu.2021.716710
Received
01 June 2021
Accepted
18 August 2021
Published
03 September 2021
Volume
12 - 2021
Edited by
Ignacio Melero, University of Navarra, Spain
Reviewed by
Cristina Maccalli, Sidra Medicine, Qatar; Jinyang Li, The Rockefeller University, United States
Updates
Copyright
© 2021 Qiu, Shao, Wen, Jiang, Ma, Wang, Huang, Ding and Zhang.
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: Longzhen Zhang, jsxyfyzlz@126.com; Xin Ding, dingxin81@163.com
†These authors have contributed equally to this work and share first authorship
This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology
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.