2012Chinese Journal of Otorhinolaryngology-skull Base SurgeryRequires access

Effect of rh-endostatin on proliferation and apoptosis of nasopharyngeal carcinoma cell CNE2

Tiesong Zhang

Open publisher page 0 citations

Abstract

Objective To evaluate the inhibitory effect and the possible mechanism of rh-endostatin(rh-ES) on nasopharyngeal carcinoma cells(CNE2).Methods CNE2 cells were treated with rh-ES of different concentrations(25,50,100,200 and 400 μg /ml,respectively) in vitro.Methyl thiazolyl tetrazolium(MTT) assay was used for detecting the cell proliferation in rh-ES treatment at different concentrations and different time intervals.Flow cytometry was used for detecting the effect of rh-ES on cell cycle and apoptosis.Transmission electron microscope was used for observing the cellular morphology of CNE2 cells.Results ① MTT detection showed that rh-ES significantly inhibited the growth of nasopharyngeal carcinoma cell CNE2 in both time-and dose-dependent manners.72 hours after rh-ES treatment it was at 400 μg/ml,and the inhibitory rate was 41.89%,which was higher than those of the other groups.② Flow cytometry showed that the proportion of CNE2 cells arrested in G0/G1 phase and cell apoptosis rate after rh-ES treatment were significantly higher than those of the control group respectively(P0.05).③ Transmission electron microscope identified the characteristics of apoptosis appeared in CNE2 cell of rh-ES group,such as crenation of cell organ,chips of chromatin margination and disappearance of caryotheca.Conclusion By inducing apoptosis and changing the cell cycle distribution,rh-ES can inhibit the proliferation of nasopharyngeal carcinoma cell CNE2 in both time-and dose-dependent manners.

About this research paper

What this paper is about

Objective To evaluate the inhibitory effect and the possible mechanism of rh-endostatin(rh-ES) on nasopharyngeal carcinoma cells(CNE2).Methods CNE2 cells were treated with rh-ES of different concentrations(25,50,100,200 and 400 μg /ml,respectively) in vitro.Methyl thiazolyl tetrazolium(MTT) assay was used for detecting the cell proliferation in rh-ES treatment at different concentrations and different time intervals.Flow cytometry was used for detecting the effect of rh-ES on cell cycle and apoptosis.Transmission electron microscope was used for observing the cellular morphology of CNE2 cells.Results ① MTT detection showed that rh-ES significantly inhibited the growth of nasopharyngeal carcinoma cell CNE2 in both time-and dose-dependent manners.72 hours after rh-ES treatment it was at 400 μg/ml,and the inhibitory rate was 41.89%,which was higher than those of the other groups.② Flow cytometry showed that the proportion of CNE2 cells arrested in G0/G1 phase and cell apoptosis rate after rh-ES treatment were significantly higher than those of the control group respectively(P0.05).③ Transmission electron microscope identified the characteristics of apoptosis appeared in CNE2 cell of rh-ES group,such as crenation of cell organ,chips of chromatin margination and disappearance of caryotheca.Conclusion By inducing apoptosis and changing the cell cycle distribution,rh-ES can inhibit the proliferation of nasopharyngeal carcinoma cell CNE2 in both time-and dose-dependent manners.

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 evaluate the inhibitory effect and the possible mechanism of rh-endostatin(rh-ES) on nasopharyngeal carcinoma cells(CNE2).Methods CNE2 cells were treated with rh-ES of different concentrations(25,50,100,200 and 400 μg /ml,respectively) in vitro.Methyl thiazolyl tetrazolium(MTT) assay was used for detecting the cell proliferation in rh-ES treatment at different concentrations and different time intervals.Flow cytometry was used for detecting the effect of rh-ES on cell cycle and apoptosis.Transmission electron microscope was used for observing the cellular morphology of CNE2 cells.Results ① MTT detection showed that rh-ES significantly inhibited the growth of nasopharyngeal carcinoma cell CNE2 in both time-and dose-dependent manners.72 hours after rh-ES treatment it was at 400 μg/ml,and the inhibitory rate was 41.89%,which was higher than those of the other groups.② Flow cytometry showed that the proportion of CNE2 cells arrested in G0/G1 phase and cell apoptosis rate after rh-ES treatment were significantly higher than those of the control group respectively(P0.05).③ Transmission electron microscope identified the characteristics of apoptosis appeared in CNE2 cell of rh-ES group,such as crenation of cell organ,chips of chromatin margination and disappearance of caryotheca.Conclusion By inducing apoptosis and changing the cell cycle distribution,rh-ES can inhibit the proliferation of nasopharyngeal carcinoma cell CNE2 in both time-and dose-dependent manners.

Key concepts: Nasopharyngeal carcinoma, Apoptosis, Flow cytometry, Cell cycle, MTT assay, Cell growth, Cell, Chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Effect of rh-endostatin on proliferation and apoptosis of nasopharyngeal carcinoma cell CNE2 — Research Paper | ScholarLens