Effects of demethylation on the growth of human gastric carcinoma cell lines and the expression of xaf1 gene
Xu Zhang
Abstract
Xu Zhang
Abstract
AIM: To observe the effects of the demethylating agent,5-Aza-2′-deoxyctidine(5-Aza-CdR),on the proliferation,cell cycle,apoptosis and xaf1 mRNA expression of stomach cancer BGC823 cells.METHODS: The proliferation of BGC823 cells treated by different concentrations of 5-Aza-CdR was detected by MTT assay.Assessment of cell cycle and apoptosis were performed by flow cytometry(FCM);the change of xaf1 mRNA expression was semi-quantified by RT-PCR before and after 5-Aza-CdR treatment.RESULTS: The growth inhibitory effects on BGC823 cells were observed in a dose-dependent manner after exposure to 5-Aza-CdR at different concentrations(1×103,5×103,10×103 nmol/L) for different time.FCM analysis showed that the apoptosis rates in BGC823 cells [(4.53±0.21)%,(8.11±1.01)%,(11.56±0.86)%] increased significantly after exposure to 5-Aza-CdR for 72 h as compared with the control group [(0.51±0.01)%,P0.05].No expression of xaf1 gene in BGC823 cells was observed,but it was expressed after 5-Aza-CdR treatment(5×103,10×103 nmol/L).CONCLUSION: 5-Aza-CdR can inhibit the proliferation of BGC823 cells through blocking cell cycles and inducing cell apoptosis.It can also restore xaf1 gene transcription silenced by demethylation.
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 observe the effects of the demethylating agent,5-Aza-2′-deoxyctidine(5-Aza-CdR),on the proliferation,cell cycle,apoptosis and xaf1 mRNA expression of stomach cancer BGC823 cells.METHODS: The proliferation of BGC823 cells treated by different concentrations of 5-Aza-CdR was detected by MTT assay.Assessment of cell cycle and apoptosis were performed by flow cytometry(FCM);the change of xaf1 mRNA expression was semi-quantified by RT-PCR before and after 5-Aza-CdR treatment.RESULTS: The growth inhibitory effects on BGC823 cells were observed in a dose-dependent manner after exposure to 5-Aza-CdR at different concentrations(1×103,5×103,10×103 nmol/L) for different time.FCM analysis showed that the apoptosis rates in BGC823 cells [(4.53±0.21)%,(8.11±1.01)%,(11.56±0.86)%] increased significantly after exposure to 5-Aza-CdR for 72 h as compared with the control group [(0.51±0.01)%,P0.05].No expression of xaf1 gene in BGC823 cells was observed,but it was expressed after 5-Aza-CdR treatment(5×103,10×103 nmol/L).CONCLUSION: 5-Aza-CdR can inhibit the proliferation of BGC823 cells through blocking cell cycles and inducing cell apoptosis.It can also restore xaf1 gene transcription silenced by demethylation.
Key concepts: Apoptosis, Cell cycle, Molecular biology, Flow cytometry, Cell growth, Demethylation, Growth inhibition, Demethylating agent