Effects of silybinon on proliferation and apoptosis of human cervical carcinoma HeLa cells
Ling Hu
Abstract
Ling Hu
Abstract
Objective: To investigate the effects of silybin on proliferation and apoptosis of human cervical carcinoma HeLa cells. Methods: The cells were divided into the control group and the silybin groups( 200,400,800 μmol / L),each group was treated for 12,24 and 36 h. MTT method was used to detect the survival rate of cells; adhesion assay was used to determinate the adhesive rate of cells; TUNEL was used to detect the apoptotic rate of cells; Caspase-Glo3 /7 kits were used to detected the activity of Caspase3 /7. Results: ① The MTT results showed that silybin could inhibit the proliferation of HeLa cells on dose and time-dependent manners,the effect of 800 μmol/L silybin( 36 h) was the most obvious( P 0. 01). ②The adhesion experiment results showed that( 24 h) silybin significantly weakened the adhesive capacity of HeLa cells on dose-dependent manner( P 0. 01). ③The TUNEL results showed silybin( 24 h) could significantly increased the apoptotic rate of HeLa cells( P 0. 01). ④ In addition,after being treated with silybin( 24 h),the apoptotic rate of cells and the activity of Caspase3 /7 increased significantly( P 0. 01). Conclusion: Silybin treatment can effectively inhibit the proliferation of HeLa cells,the mechanisms of which are related to the activation of Caspase3 /7,silybin may be a potential new drug in treatment of cervical cancer.
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 investigate the effects of silybin on proliferation and apoptosis of human cervical carcinoma HeLa cells. Methods: The cells were divided into the control group and the silybin groups( 200,400,800 μmol / L),each group was treated for 12,24 and 36 h. MTT method was used to detect the survival rate of cells; adhesion assay was used to determinate the adhesive rate of cells; TUNEL was used to detect the apoptotic rate of cells; Caspase-Glo3 /7 kits were used to detected the activity of Caspase3 /7. Results: ① The MTT results showed that silybin could inhibit the proliferation of HeLa cells on dose and time-dependent manners,the effect of 800 μmol/L silybin( 36 h) was the most obvious( P 0. 01). ②The adhesion experiment results showed that( 24 h) silybin significantly weakened the adhesive capacity of HeLa cells on dose-dependent manner( P 0. 01). ③The TUNEL results showed silybin( 24 h) could significantly increased the apoptotic rate of HeLa cells( P 0. 01). ④ In addition,after being treated with silybin( 24 h),the apoptotic rate of cells and the activity of Caspase3 /7 increased significantly( P 0. 01). Conclusion: Silybin treatment can effectively inhibit the proliferation of HeLa cells,the mechanisms of which are related to the activation of Caspase3 /7,silybin may be a potential new drug in treatment of cervical cancer.
Key concepts: HeLa, Apoptosis, TUNEL assay, MTT assay, Cervical carcinoma, Adhesion, Molecular biology, Medicine