2013Zhongguo shiyan fangjixue zazhiRequires access

Effect of Matrine Modification X on Apoptosis of Human Nasopharyngeal Carcinoma CNE1 Cells

Chen Jun

Open publisher page 0 citations

Abstract

Objective:To investigate the effects and mechanism of matrine modification X on inducing apoptosis of human nasopharyngeal carcinoma CNE1 cells in vitro.Method:MTT assay was used to measure the anti-proliferative effect of modification X on CNE1.The cell apoptosis rates and cell cycle were analyzed by flow cytometry.The protein expression of Bax,Bcl-2 and p53 was examined by Western blot.Result:After incubation of CNE1 cells with modification X for 48 h,the modification X could inhibit the proliferation of CNE1 cells with a dose dependent manner.Flow cytometry analysis revealed the apoptosis rate in 58,116 μmol.L-1 modification X group was higher than the matrine group by 70.02% and 75.73% respectively,which showed the significant difference compared with the control group(P 0.05,P 0.01).Compared with the control group,Modification X could significantly arrest the cell cycle at G1 stage(P 0.05,P 0.01).Western blot showed that the expression of Bax and p53 protein significantly increased by modification X in CNE1 cells,at the same time,the expression of Bcl-2 significantly decreased by modification X with a concentration dependent manner(P 0.05,P 0.01).Conclusion:Modification X could induce apoptosis of CNE1 cells in vitro,and the possible mechanism is related to arresting the cell cycle,increasing the Bax and p53 protein expression level and decreasing the Bcl-2 protein expression level.

About this research paper

What this paper is about

Objective:To investigate the effects and mechanism of matrine modification X on inducing apoptosis of human nasopharyngeal carcinoma CNE1 cells in vitro.Method:MTT assay was used to measure the anti-proliferative effect of modification X on CNE1.The cell apoptosis rates and cell cycle were analyzed by flow cytometry.The protein expression of Bax,Bcl-2 and p53 was examined by Western blot.Result:After incubation of CNE1 cells with modification X for 48 h,the modification X could inhibit the proliferation of CNE1 cells with a dose dependent manner.Flow cytometry analysis revealed the apoptosis rate in 58,116 μmol.L-1 modification X group was higher than the matrine group by 70.02% and 75.73% respectively,which showed the significant difference compared with the control group(P 0.05,P 0.01).Compared with the control group,Modification X could significantly arrest the cell cycle at G1 stage(P 0.05,P 0.01).Western blot showed that the expression of Bax and p53 protein significantly increased by modification X in CNE1 cells,at the same time,the expression of Bcl-2 significantly decreased by modification X with a concentration dependent manner(P 0.05,P 0.01).Conclusion:Modification X could induce apoptosis of CNE1 cells in vitro,and the possible mechanism is related to arresting the cell cycle,increasing the Bax and p53 protein expression level and decreasing the Bcl-2 protein expression level.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective:To investigate the effects and mechanism of matrine modification X on inducing apoptosis of human nasopharyngeal carcinoma CNE1 cells in vitro.Method:MTT assay was used to measure the anti-proliferative effect of modification X on CNE1.The cell apoptosis rates and cell cycle were analyzed by flow cytometry.The protein expression of Bax,Bcl-2 and p53 was examined by Western blot.Result:After incubation of CNE1 cells with modification X for 48 h,the modification X could inhibit the proliferation of CNE1 cells with a dose dependent manner.Flow cytometry analysis revealed the apoptosis rate in 58,116 μmol.L-1 modification X group was higher than the matrine group by 70.02% and 75.73% respectively,which showed the significant difference compared with the control group(P 0.05,P 0.01).Compared with the control group,Modification X could significantly arrest the cell cycle at G1 stage(P 0.05,P 0.01).Western blot showed that the expression of Bax and p53 protein significantly increased by modification X in CNE1 cells,at the same time,the expression of Bcl-2 significantly decreased by modification X with a concentration dependent manner(P 0.05,P 0.01).Conclusion:Modification X could induce apoptosis of CNE1 cells in vitro,and the possible mechanism is related to arresting the cell cycle,increasing the Bax and p53 protein expression level and decreasing the Bcl-2 protein expression level.

Key concepts: Matrine, Apoptosis, Flow cytometry, Nasopharyngeal carcinoma, Western blot, Cell cycle, Molecular biology, MTT assay

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of Matrine Modification X on Apoptosis of Human Nasopharyngeal Carcinoma CNE1 Cells — Research Paper | ScholarLens