2006Di-Si Junyi Daxue xuebaoRequires access

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

Open publisher page 0 citations

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.

About this research paper

What this paper is about

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.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Transfection, Small interfering RNA, Apoptosis, RNA interference, Cell growth, Blot, Viability assay, Cell

Related papers

Back to paper searchBrowse research topicsOriginal source
Inhibitory effect of siRNA targeting COX-2 on the growth of gastric carcinoma cells of well, moderate or poor differentiation and its mechanism — Research Paper | ScholarLens