Effects of siRNA-mediated silencing of Bmi-1 gene expression on proliferation of gastric cancer cells

Author:

Guo Ying1,Zhang Li2,Zhou Guangyu1,Ma Qingjie3ORCID,Gao Shi3,Zhao Yue4

Affiliation:

1. Department of Nephrology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China

2. Department of Neurology, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China

3. Department of Nuclear Medicine, China-Japan Union Hospital, Jilin University, Changchun, Jilin, China

4. College of Basic Medical Sciences, Jilin University, Changchun, Jilin, China

Abstract

This study was designed to investigate the effects of siRNA-mediated silencing of Bmi-1 gene expression on proliferation of AGS gastric cancer cell. siRNA Bmi-1 was transfected into human AGS gastric cancer cells by liposome (as siRNA Bmi-1 group) with negative control (as control group); the expressions of Bmi-1 and apoptosis-related genes like P21, Bax, and Bcl-2 in AGS cells were determined by Western blot method; the apoptosis of AGS cells was detected by flow cytometry double staining and Hoechst staining; and cell cycle was measured by flow cytometry. Compared with the control group, the expression of Bmi-1 in the siRNA Bmi-1 group was significantly decreased ( P < 0.05), the apoptosis rate was increased ( P < 0.05), and cell cycles were arrested at G1 phase (P < 0.05); the expression level of P21 and Bax in cells was significantly up-regulated while that of Bcl-2 down-regulated ( P < 0.05). The down regulation of Bmi-1 can inhibit the proliferation of AGS gastric cancer cell and promote its apoptosis, which takes such effects mainly by up-regulating P21 as well as Bax and down-regulating Bcl-2.

Publisher

SAGE Publications

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