2011Molecular Medicine ReportsOpen access

Down-regulation of osteopontin expression by RNA interference affects cell proliferation and chemotherapy sensitivity of breast cancer MDA-MB-231 cells

Wenshu Zuo

Open full text 37 citations

Abstract

To determine the effect of the down-regulation of osteopontin (OPN) expression on the sensitivity of breast cancer cells to doxorubicin, a chemotherapeutic drug, OPN shRNA was used to transfect the OPN-positive breast cancer cell line MDA-MB-231. The expression of OPN mRNA and protein was analyzed by RT-PCR and Western blotting, respectively. The cell cycle distribution and apoptosis were analyzed by flow cytometry. Transfected MDA-MB-231 cells were treated with different concentrations of doxorubicin. Growth of MDA-MB-231 cells and IC50 of doxorubicin were determined by MTT assay. Expression of OPN mRNA and OPN protein of cells transfected with OPN shRNA was significantly decreased when compared to the negative controls (P<0.05). The number of MDA-MB-231 cells in the S phase was significantly increased, from 22.77 to 43.67%. Transfection increased apoptosis from 3.61 to 4.91%. Furthermore, the proliferation of MDA-MB-231 cells transfected with OPN shRNA was significantly decreased when compared to the negative control (transfected with empty vector). Sensitivity of MDA-MB-231 cells to doxorubicin was enhanced after treatment with OPN shRNA. The IC50 values of doxorubicin of the OPN-transfected group, the MDA-MB-231 cells and the negative transfected group were 0.13588, 0.83869 and 0.79652 µg/ml, respectively. Down-regulation of OPN significantly inhibits expression of OPN protein in MDA-MB-231 breast cancer cells, reduces cell proliferation and increases their sensitivity to doxorubicin.

Open-access reader

About this research paper

What this paper is about

To determine the effect of the down-regulation of osteopontin (OPN) expression on the sensitivity of breast cancer cells to doxorubicin, a chemotherapeutic drug, OPN shRNA was used to transfect the OPN-positive breast cancer cell line MDA-MB-231. The expression of OPN mRNA and protein was analyzed by RT-PCR and Western blotting, respectively. The cell cycle distribution and apoptosis were analyzed by flow cytometry. Transfected MDA-MB-231 cells were treated with different concentrations of doxorubicin. Growth of MDA-MB-231 cells and IC50 of doxorubicin were determined by MTT assay. Expression of OPN mRNA and OPN protein of cells transfected with OPN shRNA was significantly decreased when compared to the negative controls (P<0.05). The number of MDA-MB-231 cells in the S phase was significantly increased, from 22.77 to 43.67%. Transfection increased apoptosis from 3.61 to 4.91%. Furthermore, the proliferation of MDA-MB-231 cells transfected with OPN shRNA was significantly decreased when compared to the negative control (transfected with empty vector). Sensitivity of MDA-MB-231 cells to doxorubicin was enhanced after treatment with OPN shRNA. The IC50 values of doxorubicin of the OPN-transfected group, the MDA-MB-231 cells and the negative transfected group were 0.13588, 0.83869 and 0.79652 µg/ml, respectively. Down-regulation of OPN significantly inhibits expression of OPN protein in MDA-MB-231 breast cancer cells, reduces cell proliferation and increases their sensitivity to doxorubicin.

Why it matters

OpenAlex reports 37 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

To determine the effect of the down-regulation of osteopontin (OPN) expression on the sensitivity of breast cancer cells to doxorubicin, a chemotherapeutic drug, OPN shRNA was used to transfect the OPN-positive breast cancer cell line MDA-MB-231. The expression of OPN mRNA and protein was analyzed by RT-PCR and Western blotting, respectively. The cell cycle distribution and apoptosis were analyzed by flow cytometry. Transfected MDA-MB-231 cells were treated with different concentrations of doxorubicin. Growth of MDA-MB-231 cells and IC50 of doxorubicin were determined by MTT assay. Expression of OPN mRNA and OPN protein of cells transfected with OPN shRNA was significantly decreased when compared to the negative controls (P<0.05). The number of MDA-MB-231 cells in the S phase was significantly increased, from 22.77 to 43.67%. Transfection increased apoptosis from 3.61 to 4.91%. Furthermore, the proliferation of MDA-MB-231 cells transfected with OPN shRNA was significantly decreased when compared to the negative control (transfected with empty vector). Sensitivity of MDA-MB-231 cells to doxorubicin was enhanced after treatment with OPN shRNA. The IC50 values of doxorubicin of the OPN-transfected group, the MDA-MB-231 cells and the negative transfected group were 0.13588, 0.83869 and 0.79652 µg/ml, respectively. Down-regulation of OPN significantly inhibits expression of OPN protein in MDA-MB-231 breast cancer cells, reduces cell proliferation and increases their sensitivity to doxorubicin.

Key concepts: Transfection, Osteopontin, Cell cycle, Small hairpin RNA, Apoptosis, Cell growth, Doxorubicin, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
Down-regulation of osteopontin expression by RNA interference affects cell proliferation and chemotherapy sensitivity of breast cancer MDA-MB-231 cells — Research Paper | ScholarLens