Effect of 5-Aza-2'-deoxycytidine on human renal cell carcinoma cell line OS-RC-2
Zhou Liu-zheng
Abstract
Zhou Liu-zheng
Abstract
Objective To study the influence of 5-Aza-2'-deoxycytidine(5-Aza-CdR)on the proliferation and apoptosis of human renal carcinoma OS-RC-2 cell line.Methods Human renal carcinoma OS-RC-2 cells were treated with a cocentration of 10-7,10-6,10-5 or 10-4mol/L 5-Aza-CdR,respectively.The growth rate of the cells was detected by MTT assay and ultrastructural changes were observed under transmissional electron microscope.The apoptosis was analyzed by flow cytometry. Results 5-Aza-CdR inhibited the proliferation of OS-RC-2 cells in a time-and concentration-dependent manner(P0.05).There were significant increases in apoptotic rates of OS-RC-2 cells [(3.74±0.34)%,(7.85±0.59)%,(12.93±1.32)% vs.(0.86±0.08)%](P0.01) after 5-Aza-CdR treatment.The cells number of G0/G1 phase increased at a concentration of 10-6 mol/L(P0.05),and the cell cycle was stopped at G0/G1 phase after treated for 3 days. The methylation status of γ-catenin gene promoter region was reversed with 5-Aza-CdR 10-5mol/L treating for 72h.Conclusion 5-Aza-CdR can inhibit the growth of OS-RC-2 cells and promote their apoptosis by elimilating demethylation of γ-catenin gene CpG-rich promoter regions.
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 study the influence of 5-Aza-2'-deoxycytidine(5-Aza-CdR)on the proliferation and apoptosis of human renal carcinoma OS-RC-2 cell line.Methods Human renal carcinoma OS-RC-2 cells were treated with a cocentration of 10-7,10-6,10-5 or 10-4mol/L 5-Aza-CdR,respectively.The growth rate of the cells was detected by MTT assay and ultrastructural changes were observed under transmissional electron microscope.The apoptosis was analyzed by flow cytometry. Results 5-Aza-CdR inhibited the proliferation of OS-RC-2 cells in a time-and concentration-dependent manner(P0.05).There were significant increases in apoptotic rates of OS-RC-2 cells [(3.74±0.34)%,(7.85±0.59)%,(12.93±1.32)% vs.(0.86±0.08)%](P0.01) after 5-Aza-CdR treatment.The cells number of G0/G1 phase increased at a concentration of 10-6 mol/L(P0.05),and the cell cycle was stopped at G0/G1 phase after treated for 3 days. The methylation status of γ-catenin gene promoter region was reversed with 5-Aza-CdR 10-5mol/L treating for 72h.Conclusion 5-Aza-CdR can inhibit the growth of OS-RC-2 cells and promote their apoptosis by elimilating demethylation of γ-catenin gene CpG-rich promoter regions.
Key concepts: Apoptosis, Flow cytometry, Molecular biology, Cell cycle, Deoxycytidine, Cell culture, Cell growth, MTT assay