2005•Chinese Clinical OncologyRequires access

The relationship between PCNA and cell apoptosis in human breast cancer

Wenwu Wang

Open publisher page 0 citations

Abstract

Objective:To investigate the relationship between proliferating cell nuclear antigen(PCNA) and cell apoptosis in human breast cancer.Methods:MTT colorimetric assay was applied to examine the growth inhibition,and apoptosis rates were determined by terminal-deoxynucleotidyl transferase mediated d-UTP nick end labeling(Tunel);The expressive levels of dephosphorylated RB protein and PCNA were detected with immunocytochemistry.Results:MTT assay that ADR inhibited proliferation of MCF-7/S cells in a dose dependent manner,the 50% inhibition concentration (IC_50 ) was 0.128mg/L.Tumor cell apoptotic rate(AR) in ADR group(=0.261) was significantly higher than that in control group (=0.0449,P0.01),PCNA positive expression rate in ADR group (=0.3371) was significantly lower than that in control group (=0.5152,P0.01).Conclusion:There was significant negative association between AR and PCAN in ADR group and control group;ADR could include MCF-7/S cells apoptosis and inhibit MCF-7/S cells proliferation.

About this research paper

What this paper is about

Objective:To investigate the relationship between proliferating cell nuclear antigen(PCNA) and cell apoptosis in human breast cancer.Methods:MTT colorimetric assay was applied to examine the growth inhibition,and apoptosis rates were determined by terminal-deoxynucleotidyl transferase mediated d-UTP nick end labeling(Tunel);The expressive levels of dephosphorylated RB protein and PCNA were detected with immunocytochemistry.Results:MTT assay that ADR inhibited proliferation of MCF-7/S cells in a dose dependent manner,the 50% inhibition concentration (IC_50 ) was 0.128mg/L.Tumor cell apoptotic rate(AR) in ADR group(=0.261) was significantly higher than that in control group (=0.0449,P0.01),PCNA positive expression rate in ADR group (=0.3371) was significantly lower than that in control group (=0.5152,P0.01).Conclusion:There was significant negative association between AR and PCAN in ADR group and control group;ADR could include MCF-7/S cells apoptosis and inhibit MCF-7/S cells proliferation.

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 relationship between proliferating cell nuclear antigen(PCNA) and cell apoptosis in human breast cancer.Methods:MTT colorimetric assay was applied to examine the growth inhibition,and apoptosis rates were determined by terminal-deoxynucleotidyl transferase mediated d-UTP nick end labeling(Tunel);The expressive levels of dephosphorylated RB protein and PCNA were detected with immunocytochemistry.Results:MTT assay that ADR inhibited proliferation of MCF-7/S cells in a dose dependent manner,the 50% inhibition concentration (IC_50 ) was 0.128mg/L.Tumor cell apoptotic rate(AR) in ADR group(=0.261) was significantly higher than that in control group (=0.0449,P0.01),PCNA positive expression rate in ADR group (=0.3371) was significantly lower than that in control group (=0.5152,P0.01).Conclusion:There was significant negative association between AR and PCAN in ADR group and control group;ADR could include MCF-7/S cells apoptosis and inhibit MCF-7/S cells proliferation.

Key concepts: Proliferating cell nuclear antigen, TUNEL assay, Apoptosis, Terminal deoxynucleotidyl transferase, Cell growth, Medicine, MTT assay, Immunocytochemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
The relationship between PCNA and cell apoptosis in human breast cancer — Research Paper | ScholarLens