Di Liu, Peng Xia, Dongmei Diao, Yao Cheng, Hao Zhang, Dawei Yuan, Chen Huang, Chengxue Dang. MiRNA-429 suppresses the growth of gastric cancer cells in vitro[J]. The Journal of Biomedical Research, 2012, 26(5): 389-393. DOI: 10.7555/JBR.26.20120029
Citation:
Di Liu, Peng Xia, Dongmei Diao, Yao Cheng, Hao Zhang, Dawei Yuan, Chen Huang, Chengxue Dang. MiRNA-429 suppresses the growth of gastric cancer cells in vitro[J]. The Journal of Biomedical Research, 2012, 26(5): 389-393. DOI: 10.7555/JBR.26.20120029
Di Liu, Peng Xia, Dongmei Diao, Yao Cheng, Hao Zhang, Dawei Yuan, Chen Huang, Chengxue Dang. MiRNA-429 suppresses the growth of gastric cancer cells in vitro[J]. The Journal of Biomedical Research, 2012, 26(5): 389-393. DOI: 10.7555/JBR.26.20120029
Citation:
Di Liu, Peng Xia, Dongmei Diao, Yao Cheng, Hao Zhang, Dawei Yuan, Chen Huang, Chengxue Dang. MiRNA-429 suppresses the growth of gastric cancer cells in vitro[J]. The Journal of Biomedical Research, 2012, 26(5): 389-393. DOI: 10.7555/JBR.26.20120029
Department of Surgical Oncology, the First Affiliated Hospital, Medical School of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, China
2.
Department of Genetics and Molecular Biology, Medical School of Xi'an Jiaotong University/Key Laboratory of Environment and Genes Related Diseases of Ministry of Education, Xi'an, Shaanxi 710061, China
Funds:
National Natural Science Foundation of China (No.30973489)
Micro-RNAs (miRNAs) have been found to be implicated in a very wide range of physiological processes. This study was aimed to investigate the regulation of miRNA-429 (miR-429) in gastric cancer cells on cell proliferation and apoptosis. Quantitative PCR was employed to detect the expressions of miR-429 after eukaryotic expression plasmid of miR-429 and its inhibitor were transiently transfected into poorly differentiated human gastric cancer cell line BGC823. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) reduction assays were used to examine proliferation ability. Apoptosis was analyzed by flow cytometry after transfection. The results showed that 48 h after transfection, overexpression of miR-429 reached maximum efficiency. Compared with mock transfection, miR-429 inhibited tumor cell proliferation significantly (P < 0.05) at 48 h and 72 h. of Overexpression of miR-429 promoted tumor cell apoptosis when compared with mock transfected cells (P < 0.05). On the contrary, miR-429 inhibitor promoted tumor cell proliferation and inhibited apoptosis when compared with controls (P < 0.05). Our results suggested that miRNA-429 may serve as a tumor suppressor during tumorigenesis of gastric cancer and may be a potential gastric cancer therapeutic target.
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