2011•Chinese Journal of Laboratory DiagnosisRequires access

Induce apoptosis effect of Ginseng Rh2 on HepG2 cells

Shaowen Chen

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Abstract

Objective To investigate the effects of genoside Rh2 on inducing hepatocellular carcinoma cell hepG2 apoptosis in vitro.Methods MFC cells were divided into four gourps:cont rol group and G-Rh2(5,10,20 mg/L) groups.The cell viability was determined by MTT;the cell cycle was detected by flow cytomet ry;the gene expression of survivin was observed by RT-PCR.Results Compared with cont rol group,the cell viabilities decreased gradually with the increasing of dose and time in G-Rh2(5,10,20 mg/L) groups at different time(24,48,72 h)(P0.05),the ratio of FCM G0/G1 cells increased and S cells decreased(P0.05),at the same time,the expression level of surviving decreased in a dose2dependent manner(P0.05).Conclusion G-Rh2 can decease cell viability by inducing apoptosis and arresting cell cycle,and the process may associate with survivin decrease.

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What this paper is about

Objective To investigate the effects of genoside Rh2 on inducing hepatocellular carcinoma cell hepG2 apoptosis in vitro.Methods MFC cells were divided into four gourps:cont rol group and G-Rh2(5,10,20 mg/L) groups.The cell viability was determined by MTT;the cell cycle was detected by flow cytomet ry;the gene expression of survivin was observed by RT-PCR.Results Compared with cont rol group,the cell viabilities decreased gradually with the increasing of dose and time in G-Rh2(5,10,20 mg/L) groups at different time(24,48,72 h)(P0.05),the ratio of FCM G0/G1 cells increased and S cells decreased(P0.05),at the same time,the expression level of surviving decreased in a dose2dependent manner(P0.05).Conclusion G-Rh2 can decease cell viability by inducing apoptosis and arresting cell cycle,and the process may associate with survivin decrease.

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Available abstract

Objective To investigate the effects of genoside Rh2 on inducing hepatocellular carcinoma cell hepG2 apoptosis in vitro.Methods MFC cells were divided into four gourps:cont rol group and G-Rh2(5,10,20 mg/L) groups.The cell viability was determined by MTT;the cell cycle was detected by flow cytomet ry;the gene expression of survivin was observed by RT-PCR.Results Compared with cont rol group,the cell viabilities decreased gradually with the increasing of dose and time in G-Rh2(5,10,20 mg/L) groups at different time(24,48,72 h)(P0.05),the ratio of FCM G0/G1 cells increased and S cells decreased(P0.05),at the same time,the expression level of surviving decreased in a dose2dependent manner(P0.05).Conclusion G-Rh2 can decease cell viability by inducing apoptosis and arresting cell cycle,and the process may associate with survivin decrease.

Key concepts: Survivin, Apoptosis, Viability assay, Cell cycle, Flow cytometry, Cell, Ginseng, MTT assay

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