2014•Academic Journal of Chinese PLA Medical SchoolRequires access

Mechanism of Syngrathus protein extract underlying apoptosis of cervical cancer Hela cells

Yuxi Liu

Open publisher page 1 citations

Abstract

Objective To study the role of Syngrathus protein extract in inducing proliferation and apoptosis of cervical cancer Hela cells. Methods The inhibitory effect of Syngrathus protein extract on growth of Hela cells was tested by MTT assay. Apoptosis of Hela cells was assayed by Annexin V/PI flow cytometry. Expression of Bax, p53 and Bcl-2 in Hela cells was detected by Western blot. Results Syngrathus protein extract inhibited the growth of Hela cells in a time- and concentration-dependent manner. Annexin V/PI flow cytometry showed that the early and late apoptosis rate of Hela cells were significantly higher in Syngrathus protein extract treatment group than in control group(29.18±0.65, 39.32±0.78, 51.21±1.13, 61.56±1.09 vs 9.82±0.18, P0.05; 3.20±0.03, 7.48±0.06, 11.11±0.07, 14.60±0.03 vs 1.12±0.09, P0.05). Western blot displayed that the expression level of Bax and P53 protein increased while that of Bcl-2 protein decreased with the increasing concentration of Syngrathus protein extract. ConclusionSyngrathus protein extract inhibits the proliferation and induces the apoptosis of Hela cells in vitro by up-regulating the expression of Bax and P53 and down-regulating the expression of Bcl-2. The apoptosis rate of Hela cells increases with the increasing concentration of Syngrathus protein extract.

About this research paper

What this paper is about

Objective To study the role of Syngrathus protein extract in inducing proliferation and apoptosis of cervical cancer Hela cells. Methods The inhibitory effect of Syngrathus protein extract on growth of Hela cells was tested by MTT assay. Apoptosis of Hela cells was assayed by Annexin V/PI flow cytometry. Expression of Bax, p53 and Bcl-2 in Hela cells was detected by Western blot. Results Syngrathus protein extract inhibited the growth of Hela cells in a time- and concentration-dependent manner. Annexin V/PI flow cytometry showed that the early and late apoptosis rate of Hela cells were significantly higher in Syngrathus protein extract treatment group than in control group(29.18±0.65, 39.32±0.78, 51.21±1.13, 61.56±1.09 vs 9.82±0.18, P0.05; 3.20±0.03, 7.48±0.06, 11.11±0.07, 14.60±0.03 vs 1.12±0.09, P0.05). Western blot displayed that the expression level of Bax and P53 protein increased while that of Bcl-2 protein decreased with the increasing concentration of Syngrathus protein extract. ConclusionSyngrathus protein extract inhibits the proliferation and induces the apoptosis of Hela cells in vitro by up-regulating the expression of Bax and P53 and down-regulating the expression of Bcl-2. The apoptosis rate of Hela cells increases with the increasing concentration of Syngrathus protein extract.

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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 study the role of Syngrathus protein extract in inducing proliferation and apoptosis of cervical cancer Hela cells. Methods The inhibitory effect of Syngrathus protein extract on growth of Hela cells was tested by MTT assay. Apoptosis of Hela cells was assayed by Annexin V/PI flow cytometry. Expression of Bax, p53 and Bcl-2 in Hela cells was detected by Western blot. Results Syngrathus protein extract inhibited the growth of Hela cells in a time- and concentration-dependent manner. Annexin V/PI flow cytometry showed that the early and late apoptosis rate of Hela cells were significantly higher in Syngrathus protein extract treatment group than in control group(29.18±0.65, 39.32±0.78, 51.21±1.13, 61.56±1.09 vs 9.82±0.18, P0.05; 3.20±0.03, 7.48±0.06, 11.11±0.07, 14.60±0.03 vs 1.12±0.09, P0.05). Western blot displayed that the expression level of Bax and P53 protein increased while that of Bcl-2 protein decreased with the increasing concentration of Syngrathus protein extract. ConclusionSyngrathus protein extract inhibits the proliferation and induces the apoptosis of Hela cells in vitro by up-regulating the expression of Bax and P53 and down-regulating the expression of Bcl-2. The apoptosis rate of Hela cells increases with the increasing concentration of Syngrathus protein extract.

Key concepts: HeLa, Apoptosis, Annexin, Flow cytometry, Western blot, Molecular biology, MTT assay, Pi

Related papers

Back to paper searchBrowse research topicsOriginal source
Mechanism of Syngrathus protein extract underlying apoptosis of cervical cancer Hela cells — Research Paper | ScholarLens