ORIGINAL RESEARCH article
MicroRNA (miR)-597-5p Inhibits Colon Cancer Cell Migration and Invasion by Targeting FOS-Like Antigen 2 (FOSL2)
- 1Department of Hepatobiliary and Pancreatic Surgery, China-Japan Union Hospital of Jilin University, Changchun, China
- 2Department of Gastrointestinal Colorectal and Anal Surgery, China-Japan Union Hospital of Jilin University, Changchun, China
- 3Medical Record Department, China Japan Union Hospital of Jilin University, Changchun, China
Our previous work had shown that FOS-like antigen 2 (FOSL2) is regulated by miR-143-5p in colorectal cancer (CRC). Given that it has been shown by others that FOSL2 is also a target of miR-597-5p in breast adenocarcinoma, the objective of the current work was to determine whether FOSL2 is regulated by miR-597-5p in CRC and the role of miR-597-5p in CRC. MiR-597-5p expression was determined in RNA obtained from 30 paired samples of colon cancer and tumor adjacent normal tissue, as well as in the LoVo (CRC cell line) and FHC (normal colonic epithelial cells) by quantitative real time polymerase chain reaction (qRT-PCR). MiR-597-5p expression was significantly downregulated in both CRC tissue and LoVo cells. Reporter assays using wild-type and miR-597-5p seed mutant FOSL2 confirmed that FOSL2 is a bona fide target of miR-597-5p. Modulating miR-597-5p expression levels in FHC and LoVo cells using antagomir and mimic, respectively, impacted expression of epithelial and mesenchymal cell markers as well as in vitro migration and invasion, without any effect on cell proliferation, showing that miR-597-5p functions as a suppressor of epithelial to mesenchymal transition. Restoration of FOSL2 expression rescued pro-metastatic functional properties of LoVo cells conforming that effect of miR-597-5p was being mediated by targeting FOSL2. Xenograft assays in athymic nude mice showed that miR-597-5p mimic did not reduce tumor incidence or growth in LoVo cells. However, using a hepatic metastasis model showed that miR-597-5p mimic can significantly prevent hepatic metastatic nodule formation as well as FOSL2 expression in these metastatic nodules. Importantly, FOSL2 mRNA and miR-597-5p expression was found to be inversely correlated in an independent cohort of 21 CRC patients Cumulatively our results show that miR-597-5p functions as a suppressor of metastatic progression in CRC by targeting FOSL2. Replenishment of miR-597-5p can be a potential therapeutic target where its expression along with FOSL2 can serve as potential diagnostic markers in CRC.
Development of chemotherapy resistance is responsible for majority of the fatalities in colorectal cancer (CRC), which contributes to ~9% of cancer mortality (1, 2). Surgical excision is the first line of treatment (3); however there is already onset of metastatic disease during diagnosis making surgical resection ineffective. Hence, additional markers for metastatic disease needs to be defined which can be potentially used for diagnosis and as therapeutic targets in CRC.
Sensitivity to pre-operative chemotherapy in CRC patients is linked to KRAS gene mutation (3, 4). Approximately 35–45% of CRC patients harbor mutations in KRAS (4–11), with exon 12 mutations accounting for 4/5th of total mutations (4). The response to neoadjuvant chemotherapy is poor when KRAS mutation is present. MicroRNAs (miRNAs) are non-coding RNAs that can bind target mRNA by complementary base pairing and inhibit translation of the mRNA. MiRNAs function as tumor suppressors and as oncogenes in CRC (12, 13). MiR-143-5p has been shown to target KRAS in CRC and prostate cancer (14, 15).
Previous work by us has shown that sensitivity of CRC cell lines to paclitaxel (PTX) treatment is dependent on KRAS mutation status and expression of miR-143-5p. LoVo cells that harbor KRAS mutation, but not SW480 cells with wild-type KRAS, were found to be sensitive to PTX treatment when miR-143-5p levels were restored by transfection of miR-143-5p mimic (16). Apart from this increased sensitivity, restoration of the miR-143-5p also caused inhibition of in vitro migration and invasion in LoVo cells (16), indicating that miR-143-5p regulates a pro-mesenchymal switch in these cells. Subsequent work by us showed that FOSL2 was downregulated in LoVo cells when miR-143-5p was restored (17).
It has been recently shown that miR-597-5p targets FOSL2 in normal breast epithelial cells and downregulation of miR-597-5p during breast cancer prognosis promote migratory behavior in breast cancer cells (18). Hence, the objective of the current study was to determine of miR-597-5p targets FOSL2 in the context of CRC.
Patient Samples, Tissue Storage, Isolation of RNA, and Quantitative Real Time PCR (qRT-PCR)
The China Japan Union Hospital of Jilin University was the source of 30 paired samples (tumor samples from surgical resection and surrounding healthy tissues) collected retrospectively. Informed consent for using tissues for research was obtained from all enrolled patients. The Institutional Review Board of the China Japan Union Hospital approved the study. This study utilized samples from patients who did not display any co-morbid manifestations; tissues were subjected to snap freezing and liquid nitrogen storage. For the independent testing, paired samples were collected from 21 CRC patients undergoing surgical resection who did not have any comorbidities or did not undergo any neoadjuvant chemotherapy. Total RNA from the samples was isolated with TriZol as per instructions of the manufacturer (ThermoFisher Scientific, Shanghai, China). Quantitative RT-PCR was done using TaqMan miRNA or TaqMan gene expression probes (ThermoFisher Scientific) for FOSL2, miR-597-5p (Assay ID: 001551), and miR-143-5p (Assay ID: 002146) as described before (16). Internal controls were RNU6B (Assay ID: 001093) and ACTB (Assay ID: Hs03023943_g1) for data normalization for miRNA and mRNA expressions, respectively. –ΔΔCt method was utilized for data analysis that was expressed as mean ± standard deviation (SD).
LoVo (mutant KRAS—G13D, A14V, wild-type BRAF, PIK3CA, PTEN, and TP53) (19) and the FHC (normal colonic epithelial cells) were obtained from the ATCC (Manassas, VA, USA) kept in a CO2 incubator at 37°C. Dulbecco's modified Eagle's media (DMEM) containing 10% fetal bovine serum (FBS) and penicillin-streptomycin (1%) was used to culture LoVo cells. The FHC was cultured using in DMEM/F12 media containing 10% FBS, 10 ng/ml cholera toxin, 10 mM HEPES, insulin and transferrin both at 0.005 mg/ml plus 100 ng/ml hydrocortisone.
Reporter and Expression Constructs
The 3′ UTR of the endogenous FOSL2 was amplified from genomic DNA using 5′- gtcctcctcgctcctcctt−3′ and 5′–tgctactcaactgaaagtggaaa−3′ forward and reverse primer, respectively. The amplified 4,869 bp product was cloned into pRL vector (Promega) to construct the 3′ UTR reporter. Mutant construct of FOSL2 3′UTR was generated using deletion of the site that binds miR-597-5p seed region using site-directed mutagenesis using QuickChange II kit (Agilent) and the following primers: 5′-ccccgtggagaaagcaattcacacagctgttc-3′ and 5′-gaacagctgtgtgaattgctttctccacgggg-3′. Assays involving luciferase involved a control for transfection as well as normalization with a firefly luciferase vector (Promega). UCSC human genome reference version hg19 was used to verify sequences of all the constructs. pcDNA3-FOSL2 overexpression plasmid was described before (16).
Cell Transfection and Luciferase Assay
MiR-597-5p mimic and anti-miR-597-5p antagomir were obtained from ThermoFisher Scientific. 50 nM of the mimic or antagomir, or luciferase reporter plasmids was used for transient transfection of FHC or LoVo as shown using Lipofectamine LTX in accordance to an earlier protocol (16). Luciferase assay was performed with the Dual Luciferase Assay kit (Promega). The expression of Renilla luciferase was subjected to normalization with respect to expression of Firefly luciferase. Mean ± standard deviation (SD) was used to represent data of three independent experiments.
Preparation of Whole Cell Lysates and Immunoblot Analysis
Immunoblot analysis was done as described previously (16). Blots were probed with the following antibodies as indicated: E-cadherin (clone 4A2; catalog # 231303), Fibronectin (catalog # 2413), Vimentin (catalog # 24525), GAPDH (catalog # 9485) (Abcam, Cambridge, MA, USA), and FOSL2 (catalog # LS-C116891, Seattle, WA, USA).
MTT Assay for Cell Proliferation
Ninety-six well plates with clear bottom were used to culture cells. An assay based on colorimetry (MTT assay, Sigma-Aldrich, St. Louis, MO, USA) was used to determine cell proliferation according to manufacturer guidelines. Absorbance value at 570 nm was subjected to correction by using absorbance at 690 nm (reference) that was subtracted from the former. The relative corrected absorbance was used to determine relative proliferation, Data is represented as mean ± SD.
Transwell Migration and Invasion Assays
CytoSelect 24-Well Cell Migration and Invasion Assay (8 μm) (Cell BioLabs, San Diego, CA, USA) was utilized for these assays in accordance to instructions of the manufacturer. Images were obtained at 10X magnification. Data obtained were used to analyze percent migration and invasion and were expressed as mean ± standard deviation.
All animal experiments reported in the current study was approved by the Institutional Animal Care and Use Committee of China Japan Union Hospital of Jilin University. Xenograft assay was performed as described previously (17). For xenograft assays, 106 LoVo cells, subcutaneously injected into 8 weeks old nude mice (n = 12). Half of the animals received weekly injections of miR-597-5p mimic (13 μg/week in 100 μl volume) along with an equal volume of Lipofectamine 2000 at the original injection site. The mock group received equal volume of phosphate buffered saline instead of the miR-597-5p mimic. Tumor diameters were measured every 5 days, and volumes calculated using the estimation: width2 × length × 0.5. Animals were sacrificed on day 42 and tumor weight was measured off excised tumors. To measure metastatic potential, 5 × 105 LoVo cells were injected into the right lower lobe of the liver in mice (n = 16) as described before (17). For half of the animals, miR-597-5p mimic (13 μg/week in 100 μl volume) were administered by tail-vein injection, using equal volume mixtures of Lipofectamine 2000. The other mock group received equal volume of phosphate buffered saline instead of the miR-597-5p mimic. Animals were sacrificed on day 28 and all metastatic nodules were counted in the left lobe and data represented as mean ± SD. The liver tissues were carefully excised and fixed with 10% formalin solution. Paraffin sections (5 μm thickness) were prepared for hematoxylin-eosin (H&E) staining and immunohistochemistry (IHC) staining using anti-FOSL2 antibody using DAB chromogenic method.
Mean ± SD is the mode of expressing all the quantitative data unless specified otherwise. ANOVA with Tukey's post-hoc test was used to measure difference between groups using Origin Pro (OriginLab Corporation) with a significance level of *P < 0.05.
All patient samples collected were from Stage II and III CRC patients who had undergone surgical resection and did not have any co-morbidities. We initially determined the expression of miR-597-5p and miR-143-5p expression levels in these 30 paired samples. Expression of both miR-143-5p and miR-597-5p were downregulated compared to tumor adjacent normal tissue (P < 0.05 in each case; Figure 1A). We did not find any significant correlation of miR-597-5p expression and clinicopathological features, inclusive of age, gender, disease stage, and survival (data not shown). This can potentially be attributed to the small sample size of our study cohort. Whether miR-143-5p and miR-597-5p have redundant or overlapping roles in preventing colon cancer remains to be evaluated.
Figure 1. Down regulation of MiR-597-5p in colon cancer cells. (A) qRT-PCR analysis of miR-597-5p and miR-143-5p using RNA isolated from 30 paired cancer and tumor adjacent normal colon tissue specimens. (B) qRT-PCR analysis of miR-597-5p in LoVo and FHC cells (normal colonic epithelium). Data in (A,B) were normalized based on RNU6B expression. Data expressed as mean ± SD of three independent experiments. *P < 0.05.
We next determined the relative expression of miR-597-5p in the colon cancer cell line LoVo and the normal colonic epithelium cell line FHC cells. Similar to what was observed in CRC patient samples, expression of miR-597-5p was significantly down regulated in the LoVo cells in comparison to that of the FHC cells (P < 0.05; Figure 1B). Cumulatively, these results indicated that the expression of miR-597-5p is downregulated in colon cancer.
We next assessed whether FOSL2 is a true target of miR-597-5p in the context of colon cancer. FHC and LoVo cell lines were transfected using Renilla luciferase reporter plasmids harboring either wild-type FOSL2 3′ UTR or miR-597-5p seed mutant 3′ UTR (Figure 2A). Renilla luciferase expression was significantly inhibited in the FHC cells compared to the LoVo cells (2.5 ± 0.05 fold; P = 0.006) (Figure 2B). Of note, miR-597-5p expression is higher in FHC cells compared to the LoVo cells (Figure 1B).
Figure 2. FOSL2 is targeted by miR-597-5p in colon cells. (A) Schematic representation of complementarity of FOSL2 3′ UTR and miR-597-5p seed sequence. (B) Relative Renilla luciferase activity of constructs with wild type 3′ UTR of FOSL2 or its mutant (with deletion of miR-597-5p binding site) in FHC and LoVo cells. (C) QRT-PCR analysis of miR-597-5p in FHC and LoVo cells transfected with miR-597-5p antagomir and mimic, respectively. (D) Relative Renilla luciferase activity of constructs with wild type or mutant FOSL2 3′ UTR of in FHC and LoVo cells, alone or in combination with anti-miR-597-5p antagomir or miR-597-5p mimic, respectively. All data in (B–D) are expressed as mean ± SD of three independent experiments. *P < 0.05; NS, non-significant.
In order to confirm that the observed differential luciferase activity of the wild-type reporter was caused by targeting of the FOSL2 3′ UTR by miR-597-5p in the FHC cells, a miR-597-5p seed mutant FOSL2 reporter plasmid was generated and tested. There was no statistically significant difference between the LoVo and FHC cells in the case of the mutant construct (P > 0.05; Figure 2B). This indicated that FOSL2 is a potential target of miR-597-5p. To further confirm this observation, FHC cells were transfected with anti-miR-597-5p antagomir and LoVo cells were transfected with miR-597-5p mimic. Successful overexpression and downregulation of miR-597-5p in LoVo and FHC cells, respectively, were verified by qRT-PCR (Figure 2C). Transfection of miR-597-5p antagomir in FHC cells significantly de-repressed Renilla luciferase expression, whereas miR-597-5p mimic transfection in LoVo cells significantly attenuated Renilla luciferase expression (Figure 2D; P < 0.05 in each case compared to mock transfection). This confirmed that FOSL2 is a bona fide target of miR-597-5p in this context. Collectively, these observations are a confirmation that miR-597-5p targets FOSL2 in normal colonic epithelial cells and that its down regulation in tumorigenic colon cells results in the induction of FOSL2 expression in colon cancer cells.
We next determined expression of FOSL2 and epithelial (E-cadherin) and mesenchymal cell (Vimentin and Fibronectin) markers in FHC and LoVo cells transfected with miR-597-5p antagomir and mimic, respectively. MiR-597-5p antagomir increased FOSL2 expression in FHC cells (Figure 3A) and induced mesenchymal cell markers and downregulated E-cadherin (Figures 3A,B). Conversely, miR-597-5p mimic decreased FOSL2 protein expression in LoVo cells (Figure 3A) and induced E-cadherin, while suppressing Fibronectin and Vimentin (Figures 3A,B). Cumulatively, these results suggest that miR-597-5p inhibits epithelial to mesenchymal transition (EMT) in normal colon epithelial cells and its downregulation in CRC cells promotes EMT.
Figure 3. MiR-597-5p replenishment in the LoVo cells downregulates mesenchymal cell markers. (A) Immunoblot analysis to determine the effect of miR-597-5p replenishment in LoVo cells and inhibition in the FHC cells on FOSL2 and epithelial (E-Cadherin) and mesenchymal cell (Fibronectin and Vimentin) markers. Following stripping of blots, GAPDH was used to probe for equal loading of samples. From among three independent experiments, one representative blot is shown here. (B) Representative immunofluorescence images of E-cadherin and Vimentin in LoVo cells and FHC cells, mock transfected or co-transfected with miR-597-5p mimic and antagomir, respectively. Scale bar, 30 μm.
However, effect of modulating miR-597-5p on FOSL2 expression and EMT in FHC and LoVo cells were independent of any significant changes in proliferation (Figure 4A), indicating that miR-597-5p exclusively suppresses pro-metastatic pathways in CRC cells. To confirm the same, we performed in vitro migration and invasion assay, two prominent functional readouts of mesenchymal cells. Mir-597-5p antagomir significantly increased in vitro migration and invasion in FHC cells (Figures 4B,C; P < 0.05 in each case compared to mock transfection). Conversely, miR-597-5p antagomir significantly inhibited in vitro migration and invasion in the LoVo cells (Figures 4B,C; P < 0.05 in each case compared to mock transfection). These results cumulatively confirmed that expression of miR-597-5p has an inverse correlation with expression of EMT marker expression as well as invasion and migration of CRC cells in vitro.
Figure 4. Manipulation of miR-597-5p expression affects in vitro migration and invasion via FOSL2. (A) Proliferation of indicated cells was examined with MTT assay. Every experiment was conducted for a minimum of three times. (B,C) Representative images (B) and quantification (C) of in vitro migration and invasion, in indicated cell variants; *P < 0.05; NS, non-significant. (D) Immunoblot analysis of FOSL2 in mock transfected LoVo cells, and LoVo cells transfected with miR-597-5p mimic alone or in combination with expression plasmid encoding FOSL2. GAPDH was used as a loading control. Shown are representative blots from three experiments. (E,F) Representative images (E) and quantification (F; *P < 0.05; NS, non-significant) of in vitro migration and invasion, in mock transfected LoVo cells, and in LoVo cells transfected with miR-597-5p mimic alone or in combination with expression plasmid encoding FOSL2. Data in (A,C,E) are represented as mean ± SD.
MiRNAs have multiple mRNA targets. Hence, to determine if the effect of modulating miR-597-5p expression on EMT and in vitro migration and invasion is being mediated via FOSL2, we performed rescue experiment in the LoVo cells. LoVo cells transfected with miR-597-5p mimic were co-transfected with FOSL2 expression plasmid lacking the 3′ UTR. Successful overexpression of FOSL2 protein expression was confirmed by western blot (Figure 4D). Next, we determined the effect of FOSL2 overexpression in LoVo cells transfected with miR-507-5p mimic on in vitro migration and invasion. As shown in Figures 4B,C, miR-597-5p transfection in LoVo cells significantly downregulated in vitro migration and invasion (Figures 4D–F). However, overexpression of FOSL2 rescued both in vitro migration and invasion capacity in LoVo cells transfected with miR-597-5p (Figures 4D–F), confirming that miR-597-5p is regulating EMT and in vitro migration and invasion via targeting FOSL2.
To determine if the in vitro effect of miR-597-5p modulation on in vitro migration and invasion in LoVo cells is operant in vivo, we performed xenograft assays. LoVo cells were subcutaneously injected into athymic nude mice. Half of the animals received weekly injection of miR-597-5p mimic at the original injection sire. Tumor formation and growth was monitored. Both experimental groups formed tumors within 12 days but there was no significant difference in tumor volume after 42 days (Figure 5A), indicating that modulating miR-597-5p expression perhaps do not affect in vivo proliferation of LoVo cells. To determine if miR-597-5p mimic will affect in vivo metastasis, we used a hepatic tumor growth model. MiR-597-5p mimic significantly inhibited hepatic metastasis (Figure 5B; P < 0.05 compared to the no-mimic group) and FOSL2 expression in the non-injected liver lobes (Figures 5C,D). These results confirm that miR-597-5p is an inhibitor of metastatic progression of CRC and its downregulation promotes CRC metastasis, and that this effect is mediated by miR-597-5p-mediated regulation of FOSL2 protein expression.
Figure 5. MiR-597-5p can suppress metastatic hepatic burden but not tumor growth rate in vivo. (A) Restoration of miR-597-5p expression by mimic did not affect tumor growth as assayed in a subcutaneous tumor model (n = 12). (B,C) Mice in the miR-597-5p mimic group, compared to the mock group, had significant less hepatic tumor burden as assayed by the presence of hepatic nodules in non-injected liver lobes. (B) shows representative H&E staining (scale bar, 1 mm) and (C) is quantification of (B) (n = 8 mice/group; *P < 0.05; NS, non-significant). (D) IHC analysis of FOSL2 in non-injected hepatic lobes showed downregulation of FOSL2 expression and hepatic nodes in mice getting tail vein injection of miR-597-5p mimic. Representative images from six mice are shown. Scale bar, 10 μm.
Given that our current experiments and earlier results (17) indicated that miR-597-5p and FOSL2 have an inverse effect on EMT markers and in vitro motility in LoVo cells, we put forth a hypothesis that human colon cancer may have suppressed levels of miR-597-5p leading to FOSL2 upregulation. In order to study the association between miR-597-5p and FOSL2 in human colon cancer, we checked the expression of miR-597-5p and FOSL2 in an independent cohort of 21 CRC patients. We observed an inverse correlation between up regulation of FOSL2 levels and decreased miR-597-5p levels (R2 = 0.7478; Figure 6).
Figure 6. MiR-597-5p and FOSL2 mRNA expression show inverse correlation in colorectal cancer patients. Pearson correlation of 21 paired CRC tumor tissue and adjacent normal tissue was used to check correlation between FOSL2 and miR-597-5p. Expression was determined by qRT-PCR as described in Methods section and Figure 1 legend.
The expression of FOS and JUN isoforms is regulated by FOS-like antigen 2 (FOSL2: another name is FRA-2), FRA-2, a member of AP-1 transcription factor family (20). This protein is also crucially involved in cancer, fibrosis, differentiation of T cells, development of bones, and circadian rhythm (21–26). Another point of interest is the potential regulation of TGF-beta signaling pathway by FOSL2 (27). This pathway is involved actively in metastasis of colon cancer (28) as well as, preservation of the stem cell niche inside the tumor (29), that in turn contributes to adjuvant chemotherapy resistance. This could account for the direct effect of FOSL2 expression on motility and in vivo metastasis of the LoVo cells. Resistance to chemotherapy shows an intimate association with epithelial to mesenchymal transition (30, 31). As FOSL2 favors a mesenchymal phenotype, it is not unexpected that the expression of this factor can influence the sensitivity of colon cancer cells to PTX (16).
An engaging point is that LoVo cells that were transfected with miR-143-5p mimic showed downregulated levels of solely FOSL2 among 10 putative targets. The role of involvements of other gene(s) in resistance or sensitivity to PTX should be determined by studying tall the RNA molecules that are expressed differentially in the presence of miR-143-5p mimic. The effect of expression of FOSL2 and colon cancer cells possessing wild-type KRAS in terms of sensitivity is yet to be studied. As migration and invasion of epithelial cells of the human colon (FHC cell line) in vitro was influenced by changing levels of FOSL2, we can hypothesize that regardless of the KRAS (wild-type or mutant), the sensitivity of colon cancer cells is influenced by the expression of FOSL2.
Role of miRNAs in the pathogenesis of different cancers is being increasingly appreciated. However, to the best of our knowledge, this study is a first that shows differential regulation of FOSL2 by miR-597-5p in normal and tumorigenic colon cancer cells. It has been earlier shown that miR-597-5p is downregulated in breast cancer patients and targets FOSL2 in normal breast epithelial cells (18). It has been shown that miR-597-5p is downregulated in epithelial ovarian cancer (32) and glioblastoma (33). It has also been shown that replenishment of miR-597-5p in ovarian cancer cells sensitizes them to cisplatin treatment by targeting ABCB1 (34). Whether FOSL2 are also being targeted by miR-597-5p in normal ovarian or brain cell remains to be determined.
Our earlier work has shown that miR-143-5p replenishment in LoVo cells sensitizes them to PTX treatment by targeting FOSL2 (16). This represents a unique regulatory role of the same gene required for metastatic progression by multiple miRNAs. The regulation of FOSL2 in the context of breast cancer (18) and ABCB1 in the context of ovarian cancer (34) by miR-143-5p is yet to be studied. It will be important to establish if concomitant downregulated levels of FOSL2 along with replenishment of miR-597-5p will synergize and chemosensitizes CRC cells to PTX-mediated cytotoxicity.
Informed consent for using tissues for research duly signed from the patients was collected. The Institutional Review Board of the Hospital gave approval for the study.
SL designed the experiment. ZL and XF performed the experiments and analyzed the data. XW and BF prepared the manuscript. All authors have read the manuscript.
Conflict of Interest Statement
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.
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Keywords: colorectal cancer, CRC, FOSL2, miR-143-5p, FOS-like antigen 2
Citation: Li S, Liu Z, Fang X, Wang X and Fei B (2019) MicroRNA (miR)-597-5p Inhibits Colon Cancer Cell Migration and Invasion by Targeting FOS-Like Antigen 2 (FOSL2). Front. Oncol. 9:495. doi: 10.3389/fonc.2019.00495
Received: 08 January 2019; Accepted: 24 May 2019;
Published: 12 June 2019.
Edited by:Valeria Poli, University of Turin, Italy
Copyright © 2019 Li, Liu, Fang, Wang and Fei. 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.
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