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miR-148a promoted cell proliferation by targeting p27 in gastric cancer cells.

Shui-Long Guo | Zheng Peng | Xue Yang | Kai-Ji Fan | Hui Ye | Zhen-Hua Li | Yan Wang | Xiao-Li Xu | Jun Li | You-Liang Wang | Yan Teng | Xiao Yang
International journal of biological sciences | 2011

Accumulating evidence has shown that miRNAs are aberrantly expressed in human gastric cancer and crucial to tumorigenesis. Herein, we identified the role of miR-148a in gastric cell proliferation. miR-148a knockdown inhibited cell proliferation in gastric cancer cell lines. Conversely, miR-148a overexpression promoted cell proliferation and cell cycle progression. p27, a key inhibitor of cell cycle, was verified as the target of miR-148a, indicating miR-148a might downregulate p27 expression to promote gastric cell proliferation. Moreover, we confirmed that miR-148a expression was frequently and dramatically downregulated in human advanced gastric cancer tissues, and observed a good inverse correlation between miR-148a and p27 expression in tumor samples. Thus, our results demonstrated that miR-148a downregulation might exert some sort of antagonistic function in cell proliferation, rather than promote cell proliferation in gastric cancer.

Pubmed ID: 21552422

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SGC-7901 (tool)

RRID:CVCL_0520

Cell line SGC-7901 is a Cancer cell line with a species of origin Homo sapiens

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