Effect of Extraction of Pelagi-margarita on Proliferation and Apoptosis of Human Cervical Cancer Cell Line Caski
Jiankun Chen
Abstract
Jiankun Chen
Abstract
[Objective] To explore the effect of extraction of pelagi-margarita(EPM)on the apoptosis of cervical cancer Caski cell line.[Method] The growth inhibition rate of Caski cells was detected by MTT method,and cell apoptosis rate was analyzed by flow cytometry(FCM)using annexinV /propidium iodide(PI)double staining,cell cycle was detected by flow cytometry using PI staining.Morphologic changes of apoptotic cells were observed by fluorescence microscope,expression of intracellular Bcl-2,Bax protein was analyzed by real time PCR.[Result] EPM inhibited the proliferation of Caski cells in a dose-dependent and time-dependent manner(P0.05).After EPM treatment at 0,6,30 and 60 μg/ml for 24 h,the apoptosis rate of Caski cells was 7.6%,7.15%,18.5% and 38.9%,respectively,while the necrosis rate was 0.45%,2.85%,8.55% and 23.2%.The cells showed characteristic apoptotic morphologic changes under fluorescence microscope.Bioenergy vigor at various concentration could down-regulate the expression of Bcl-2 mRNA,meanwhile,up-regulate the expression of Bax mRNA.[Conclusion] EPM inhibits the proliferation in a dose-dependent and time-dependent manner,and induces the apoptosis of Caski cells by down-regulate the expression of Bcl-2 mRNA,meanwhile,up-regulate the expression of Bax mRNA.
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 explore the effect of extraction of pelagi-margarita(EPM)on the apoptosis of cervical cancer Caski cell line.[Method] The growth inhibition rate of Caski cells was detected by MTT method,and cell apoptosis rate was analyzed by flow cytometry(FCM)using annexinV /propidium iodide(PI)double staining,cell cycle was detected by flow cytometry using PI staining.Morphologic changes of apoptotic cells were observed by fluorescence microscope,expression of intracellular Bcl-2,Bax protein was analyzed by real time PCR.[Result] EPM inhibited the proliferation of Caski cells in a dose-dependent and time-dependent manner(P0.05).After EPM treatment at 0,6,30 and 60 μg/ml for 24 h,the apoptosis rate of Caski cells was 7.6%,7.15%,18.5% and 38.9%,respectively,while the necrosis rate was 0.45%,2.85%,8.55% and 23.2%.The cells showed characteristic apoptotic morphologic changes under fluorescence microscope.Bioenergy vigor at various concentration could down-regulate the expression of Bcl-2 mRNA,meanwhile,up-regulate the expression of Bax mRNA.[Conclusion] EPM inhibits the proliferation in a dose-dependent and time-dependent manner,and induces the apoptosis of Caski cells by down-regulate the expression of Bcl-2 mRNA,meanwhile,up-regulate the expression of Bax mRNA.
Key concepts: Apoptosis, Propidium iodide, Flow cytometry, Molecular biology, Pi, Fluorescence microscope, Cell growth, Cell culture