Inhibitory effect of siRNA targeting COX-2 on the growth of gastric carcinoma cells of well, moderate or poor differentiation and its mechanism
Ting Xiang
Abstract
Ting Xiang
Abstract
AIM: To investigate the inhibitory effect of siRNA targeting COX-2 on the growth of gastric carcinoma cells of well, moderate or poor differentiation (MKN-28, SGC-7901, BGC-823) and related mechanism. METHODS: siRNA targeting COX-2 gene was designed, siRNA-COX-2 vector was constructed and transfected into gastric carcinoma cells to induce RNA interference. The changes of COX-2 were detected with RT-PCR and Western blotting.Cell viability was detected by MTT. Cell apoptosis was judged by TUNEL and electromicroscopy, and expressions of Bax and Bcl-2 were tested by Western blot. RESULTS: Both COX-2 expression and cell growth were inhibited in SGC-7901 and BGC-823 after transfection of siRNA-COX-2 vector into the cells. But, in MKN-28 ,only COX-2 expression decreased. The obvious cell apoptosis both in SGC-7901 and BGC-823 was observed. Bax was up-regulated and Bcl-2 was down-regulated in SGC-7901 and BGC-823. In contrast, there were almost no changes in control group in vitro. CONCLUSION: RNA interference inhibits the growth of gastric carcinoma cells, which may be related to down-regulation of COX-2 and induction of cell apoptosis. The inhibitory effect of RNAi was relatively strong in SGC-7901, which indicated that the effect of siRNA was dependent on the differentiation degree of gastric carcinoma cells.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
AIM: To investigate the inhibitory effect of siRNA targeting COX-2 on the growth of gastric carcinoma cells of well, moderate or poor differentiation (MKN-28, SGC-7901, BGC-823) and related mechanism. METHODS: siRNA targeting COX-2 gene was designed, siRNA-COX-2 vector was constructed and transfected into gastric carcinoma cells to induce RNA interference. The changes of COX-2 were detected with RT-PCR and Western blotting.Cell viability was detected by MTT. Cell apoptosis was judged by TUNEL and electromicroscopy, and expressions of Bax and Bcl-2 were tested by Western blot. RESULTS: Both COX-2 expression and cell growth were inhibited in SGC-7901 and BGC-823 after transfection of siRNA-COX-2 vector into the cells. But, in MKN-28 ,only COX-2 expression decreased. The obvious cell apoptosis both in SGC-7901 and BGC-823 was observed. Bax was up-regulated and Bcl-2 was down-regulated in SGC-7901 and BGC-823. In contrast, there were almost no changes in control group in vitro. CONCLUSION: RNA interference inhibits the growth of gastric carcinoma cells, which may be related to down-regulation of COX-2 and induction of cell apoptosis. The inhibitory effect of RNAi was relatively strong in SGC-7901, which indicated that the effect of siRNA was dependent on the differentiation degree of gastric carcinoma cells.
Key concepts: Transfection, Small interfering RNA, Apoptosis, RNA interference, Cell growth, Blot, Viability assay, Cell