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MicroRNA-761 is downregulated in colorectal cancer and regulates tumor progression by targeting Rab3D
Yupeng Ren1, Gang Shi1, Peng Jiang1
1Department of Colorectal Surgery, Cancer Hospital of China Medical University, Liaoning Cancer Hospital and Institute, Shenyang, Liaoning 110042, P.R. China.
Abstract:
The purpose of the present study was to investigate the biological role of microRNA-761 (miR-761) in colorectal cancer (CRC) and the underlying mechanisms by which miR-761 regulates CRC cell proliferation and migration. Quantitative polymerase chain reaction was performed to measure miR-761 expression in CRC tumor tissues and cell lines. It was demonstrated that miR-761 expression was dramatically reduced in CRC tumor tissues and cell lines compared with in normal tissues and cell lines. Overexpression of miR-761 significantly decreased CRC cell growth and migration. Using bioinformatics analysis and luciferase reporter assays, Rab3D was identified as a novel target of miR-761. In addition, it was demonstrated that Rab3D expression was negatively correlated with miR-761. Furthermore, overexpression of Rab3D could reverse the inhibitory effects of miR-761 on cell proliferation and migration. Collectively, the present study demonstrated that miR-761 overexpression could inhibit the proliferation and migration of CRC cell lines, partly at least, via directly targeting Rab3D.
Insights
MicroRNA-761 (miR-761) is significantly reduced in colorectal cancer (CRC). Restoring miR-761 inhibits CRC cell growth and migration by targeting Rab3D.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Colorectal cancer (CRC) is a major global health concern.
- Dysregulation of microRNAs is implicated in cancer development and progression.
- The specific role of microRNA-761 (miR-761) in CRC remains largely unexplored.
Purpose of the Study:
- To elucidate the biological function of miR-761 in colorectal cancer.
- To identify the molecular mechanisms underlying miR-761's regulation of CRC cell proliferation and migration.
- To investigate potential therapeutic targets associated with miR-761 in CRC.
Main Methods:
- Quantitative polymerase chain reaction (qPCR) to assess miR-761 expression levels in CRC tissues and cell lines.
- In vitro assays to evaluate the effects of miR-761 overexpression on CRC cell proliferation and migration.
- Bioinformatics analysis and luciferase reporter assays to identify and validate direct targets of miR-761.
- Western blot analysis to confirm protein expression levels of identified targets.
Main Results:
- miR-761 expression was significantly downregulated in colorectal cancer tissues and cell lines compared to normal controls.
- Overexpression of miR-761 markedly suppressed CRC cell proliferation and migration.
- Rab3D was identified as a direct downstream target of miR-761, with inverse correlation in expression.
- Restoration of Rab3D expression attenuated the inhibitory effects of miR-761 on CRC cell behavior.
Conclusions:
- miR-761 functions as a tumor suppressor in colorectal cancer.
- miR-761 inhibits CRC cell proliferation and migration, at least partly, through direct targeting of Rab3D.
- These findings highlight miR-761 as a potential therapeutic agent for colorectal cancer treatment.
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