Inhibitory effects of RNA interference on hTERT gene in colon cancer HT-29 cells
Chao-jun Yuan, Qiyun Li, Bo Yi
Abstract
Chao-jun Yuan, Qiyun Li, Bo Yi
Abstract
Objective To explore the inhibitory effect of RNA interference on the human telomer-ase reverse transcriptase gene in colon cancer cells. Methods Colon cancer HT-29 cells were divided into control group,N-hTERT group, Lipofectamine group,and sihTERT group. The activity of telomerase,and expression of hTERT mRNA and protein were detected before and after siRNA was transfected into HT-29 cells. Flow cytometry was used to observe the proliferation and apoptosis of HT-29 cells. Results The transfection efficiency of siRNA was 60%. The activity of telomerase, the expression levels of hTERT mR-NA and protein, and apeptosis rate in sihTERT group were 0.73±0.14,0.47±0.08,0.37±0.07, and 49.5% respectively,which were significantly different from those in other three groups (P<0.01). Con-clusion siRNA targeting hTERT can specificly scilence the hTERT gene of colon cancer cells by down-regulating the expression of hTERT mRNA and protein, and suppressing the telomerase activity. RNAi can inhibit the proliferation of the cancer cells and induce their apoptosis. Key words: Colon carcinoma; Telomerase reverse transcriptase; RNA interference
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 explore the inhibitory effect of RNA interference on the human telomer-ase reverse transcriptase gene in colon cancer cells. Methods Colon cancer HT-29 cells were divided into control group,N-hTERT group, Lipofectamine group,and sihTERT group. The activity of telomerase,and expression of hTERT mRNA and protein were detected before and after siRNA was transfected into HT-29 cells. Flow cytometry was used to observe the proliferation and apoptosis of HT-29 cells. Results The transfection efficiency of siRNA was 60%. The activity of telomerase, the expression levels of hTERT mR-NA and protein, and apeptosis rate in sihTERT group were 0.73±0.14,0.47±0.08,0.37±0.07, and 49.5% respectively,which were significantly different from those in other three groups (P<0.01). Con-clusion siRNA targeting hTERT can specificly scilence the hTERT gene of colon cancer cells by down-regulating the expression of hTERT mRNA and protein, and suppressing the telomerase activity. RNAi can inhibit the proliferation of the cancer cells and induce their apoptosis. Key words: Colon carcinoma; Telomerase reverse transcriptase; RNA interference
Key concepts: Telomerase reverse transcriptase, Telomerase, Transfection, Lipofectamine, RNA interference, Molecular biology, Messenger RNA, RNA