COX-2 gene silencing suppresses tumor formation of human gastric cancer cell lines SGC-7901 in nude mice
B Wang
Abstract
B Wang
Abstract
Objective To evaluate the inhibition effect of COX-2 gene silencing on tumor growth of human gastric cancer cell lines SGC-7901 in nude mice.Methods Eukaryotic expression plasmid of shRNA target to COX-2 was constructed.The effect of inhibition was detected by RT-PCT and Western blot after transfection with liposomes.Nude mice were divided into 3 groups,5 cases were involved in every group.Group inhibition:subcutaneous implant gastric cancer cells which COX-2 expression was suppressed.Group control:subcutaneous implant normal gastric cancer cells.Group sham:subcutaneous implant gastric cancer cells that were transfected sham plasmid.Morphological,histopathology and tumor inhibition rate were evaluated after 4 weeks.Results The expression of human COX-2 gene was suppressed specific and effectively by transfection shRNA plasmid into cells.The efficiency of inhibition was 70.42%.In group control and group sham tumor formation could be found in every case.Tumor tissue average weight of these two groups were(0.49±0.017)g and(0.49±0.013)g,while only in 2 cases(2/5)tumor formation could be found in group inhibition.Tumor tissue average weight of group inhibition was(0.05±0.003)g,tumor growth was inhibited significantly(P0.01)and the inhibition rate was 89.8%.Conclusion The expression of COX-2 in human gastric cancer cell lines SGC-7901 can be inhibited specific and effectively by RNA interference that can result to tumor formation and growth suppressed obviously.
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.
Objective To evaluate the inhibition effect of COX-2 gene silencing on tumor growth of human gastric cancer cell lines SGC-7901 in nude mice.Methods Eukaryotic expression plasmid of shRNA target to COX-2 was constructed.The effect of inhibition was detected by RT-PCT and Western blot after transfection with liposomes.Nude mice were divided into 3 groups,5 cases were involved in every group.Group inhibition:subcutaneous implant gastric cancer cells which COX-2 expression was suppressed.Group control:subcutaneous implant normal gastric cancer cells.Group sham:subcutaneous implant gastric cancer cells that were transfected sham plasmid.Morphological,histopathology and tumor inhibition rate were evaluated after 4 weeks.Results The expression of human COX-2 gene was suppressed specific and effectively by transfection shRNA plasmid into cells.The efficiency of inhibition was 70.42%.In group control and group sham tumor formation could be found in every case.Tumor tissue average weight of these two groups were(0.49±0.017)g and(0.49±0.013)g,while only in 2 cases(2/5)tumor formation could be found in group inhibition.Tumor tissue average weight of group inhibition was(0.05±0.003)g,tumor growth was inhibited significantly(P0.01)and the inhibition rate was 89.8%.Conclusion The expression of COX-2 in human gastric cancer cell lines SGC-7901 can be inhibited specific and effectively by RNA interference that can result to tumor formation and growth suppressed obviously.
Key concepts: Transfection, Gene silencing, Medicine, Growth inhibition, Small hairpin RNA, Cancer, Cancer cell, Cancer research