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Updated: Mar 13, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-561 inhibits gastric cancercell proliferation and invasion by downregulating c-Myc expression
Kun Qian1, Binglang Mao2, Wei Zhang1
1Department of Gastrointestinal Surgery, The First Affiliated Hospital of Chongqing Medical University Chongqing 400016, China.
Abstract:
Gastric cancer (GC) causes nearly one million deaths worldwide each year. However, the molecular pathway of GC development remains unclear. Increasing evidences have shown that microRNAs (miRNAs) are highly associated with tumor development. However, relative little is known about the potential role of miRNAs in gastric cancer development. In the present study, we showed that miR-561 was down-regulated frequently in human GCs cell lines and tissues, and its expression was associated with tumor-node-metastasis (pTNM) stage. Enforced expression of miR-561 in GC cells inhibited cell proliferation and invasion in vitro. In contrast, knockdown of miR-561 had the opposite effect on cell proliferation and invasion. Moreover, c-Myc was identified as a potential miR-561 target. Further studies confirmed that miR-561 suppressed the expression of c-Myc by directly binding to its 3'-untranslated region. Restoration of c-Myc in miR-561-overexpressed GC cells reversed the suppressive effects of miR-561 and c-Myc was inversely correlated with miR-561 expression in GC tissues. These results demonstrate that miR-561 acts as a novel tumor suppressor in GC by targeting c-Myc gene and inhibiting GC cells proliferation and invasion. These findings contribute to current understanding of the functions of miR-561 in GC.
Insights
MicroRNA-561 (miR-561) is frequently down-regulated in gastric cancer (GC). This study reveals miR-561 acts as a tumor suppressor by inhibiting GC cell proliferation and invasion through targeting the c-Myc gene.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer (GC) is a leading cause of cancer mortality worldwide, with its molecular pathogenesis incompletely understood.
- MicroRNAs (miRNAs) are increasingly recognized for their roles in tumorigenesis, yet their specific involvement in GC requires further elucidation.
Purpose of the Study:
- To investigate the role of miR-561 in the development and progression of gastric cancer.
- To identify the molecular targets and mechanisms through which miR-561 exerts its effects in GC.
Main Methods:
- Analysis of miR-561 expression in human GC cell lines and tissues.
- In vitro experiments assessing the effects of miR-561 modulation on GC cell proliferation and invasion.
- Identification and validation of c-Myc as a direct target of miR-561 using luciferase reporter assays and Western blotting.
Main Results:
- miR-561 expression was significantly down-regulated in GC tissues and cell lines, correlating with advanced tumor-node-metastasis (pTNM) stage.
- Overexpression of miR-561 inhibited GC cell proliferation and invasion, while its knockdown promoted these processes.
- miR-561 directly targets and suppresses c-Myc expression; restoration of c-Myc reversed the anti-proliferative and anti-invasive effects of miR-561.
Conclusions:
- miR-561 functions as a novel tumor suppressor in gastric cancer.
- The miR-561/c-Myc axis plays a critical role in regulating GC cell proliferation and invasion, offering potential therapeutic targets.
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