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miR-143 Inhibits Cell Proliferation of Gastric Cancer Cells Through Targeting GATA6
Mao Guoping1, Liu Ran2, Qin Yanru1
1Department of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, P.R. China.
Abstract:
Recent studies have suggested that the dysregulation of microRNAs (miRNAs) plays a critical role in the progression of human cancers, including gastric cancer (GC). miR-143 had been reported to function as a tumor suppressor in GC. However, the exact molecular mechanism of how miR-143 participates in GC progression remains to be determined. In this present study, we revealed that the expression of miR-143 was significantly downregulated in human GC tissues and cell lines compared with normal tissues and a normal gastric epithelium cell line. In addition, upregulation of the expression of miR-143 in a GC cell line inhibited cell proliferation and induced cell cycle arrested in the G0/G1 phase. Furthermore, GATA6 was identified as a direct target of miR-143 in GC using the luciferase reporter assay. Upregulation of miR-143 inhibited the expression of GATA6 in GC cell lines. Moreover, the overexpression of GATA6 could attenuate the effect of miR-143 on cell proliferation in the GC cell lines. Collectively, these data indicated that miR-143 plays a tumor suppressor role partly through regulating the expression of GATA6 in GC. Therefore, targeting miR-143 may be a novel therapeutic method for GC.
Insights
MicroRNAs (miRNAs) are implicated in gastric cancer (GC) progression. This study shows miR-143 suppresses GC by downregulating GATA6, suggesting miR-143 as a potential therapeutic target for gastric cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA (miRNA) dysregulation is linked to human cancer progression, including gastric cancer (GC).
- Previous research indicated miR-143 acts as a tumor suppressor in GC, but its precise mechanism remains unclear.
Purpose of the Study:
- To elucidate the molecular mechanism of miR-143 in gastric cancer progression.
- To investigate the role of miR-143 and its potential targets in GC development.
Main Methods:
- Quantitative real-time PCR to assess miR-143 expression in GC tissues and cell lines.
- Luciferase reporter assay to identify direct targets of miR-143.
- Cell proliferation assays and cell cycle analysis following miR-143 or GATA6 manipulation.
Main Results:
- miR-143 expression was significantly downregulated in human GC tissues and cell lines.
- Overexpression of miR-143 inhibited GC cell proliferation and induced G0/G1 cell cycle arrest.
- GATA6 was identified as a direct target of miR-143, and its overexpression partially reversed miR-143's inhibitory effects on cell proliferation.
Conclusions:
- miR-143 functions as a tumor suppressor in gastric cancer, partly by regulating GATA6 expression.
- Targeting miR-143 presents a potential novel therapeutic strategy for gastric cancer treatment.
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