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Published on: August 23, 2019
SOX10-dependent CMTM7 expression inhibits cell proliferation and tumor growth in gastric carcinoma
Yongdong Jin1, Xianpeng Qin2, Guiqing Jia2
1Department of Medical Oncology, Sichuan Cancer Hospital & Institute, Sichuan Cancer Center, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Abstract:
Numerous studies have shown that CMTM family members have a variety of important roles in the occurrence and progression of cancer. CMTM7 has also been reported to be down-regulated in some digestive system tumors, but the expression patterns and pathological role of CMTM7 in gastric cancer remains unclear. In this study, we found that both CMTM7 and SOX10 were significantly down-regulated in gastric cancer tissues compared with paracancerous tissues, and the expression pattern of CMTM7 and SOX10 were strongly correlated (r = 0.6455, p < 0.001). Further, through bioinformatics technology and luciferase assay, we identify that SOX10 can be a transcriptional regulator of CMTM7 to mediate the expression of CMTM7 in gastric cancer. In addition, we found silencing the expression of CMTM7 can increase the proliferation and tumorigenesis of gastric cancer cells in vivo and in vitro. More interestingly, overexpression of SOX10 in cell lines stably silencing CMTM7 expression significantly inhibited the proliferation and tumor growth of gastric cancer. Therefore, our results demonstrate that CMTM7 as a tumor suppressor is down-regulated in gastric cancer, and SOX10 can regulate the proliferation and tumor formation of gastric cancer by regulating the expression of CMTM7.
Insights
CMTM7 acts as a tumor suppressor in gastric cancer, with its expression down-regulated alongside SOX10. SOX10 regulates CMTM7, impacting gastric cancer cell proliferation and tumor growth.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The CMTM family plays critical roles in cancer development.
- CMTM7 is downregulated in some digestive tumors, but its role in gastric cancer is unclear.
Purpose of the Study:
- To investigate the expression patterns and pathological role of CMTM7 in gastric cancer.
- To explore the regulatory relationship between SOX10 and CMTM7 in gastric cancer.
Main Methods:
- Analysis of CMTM7 and SOX10 expression in gastric cancer tissues.
- Bioinformatics analysis and luciferase assays to determine SOX10's regulatory role.
- In vitro and in vivo experiments assessing the impact of CMTM7 silencing and SOX10 overexpression on gastric cancer cells.
Main Results:
- Both CMTM7 and SOX10 were significantly downregulated in gastric cancer tissues and correlated positively.
- SOX10 was identified as a transcriptional regulator of CMTM7 in gastric cancer.
- Silencing CMTM7 increased gastric cancer cell proliferation and tumorigenesis, while SOX10 overexpression inhibited these processes.
Conclusions:
- CMTM7 functions as a tumor suppressor, downregulated in gastric cancer.
- SOX10 regulates gastric cancer proliferation and tumor formation by modulating CMTM7 expression, highlighting a novel regulatory pathway.
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