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[Roles of Y box-binding protein 1 in SK-BR-3 breast cancer proliferation].

作者信息

Shi Jianhong, Lü Xinrui, Wang Bing, Daudan Lin, Yanan Wang, Yuhui Bu, Zhenfeng Ma

机构信息

Central Laboratory, Affiliated Hospital of Hebei University, Baoding 071000, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2014 Sep 30;94(36):2804-7.

Abstract

OBJECTIVE

To explore the roles of Y box-binding protein 1 (YB-1) in breast cancer cell proliferation.

METHODS

Twenty cases of surgical removal of breast cancer tissue (diagnosed with invasive ductal carcinoma, stage II, by postoperative paraffin pathology) and normal breast tissues adjacent to carcinoma were collected during June 2013 to August 2013.Quantitative real-time PCR (qRT-PCR) was performed to detect the YB1 mRNA levels. Cultured mammary epithelial cells (HBL-100) and breast cancer cells (MCF7, MDA-MB-231 & SK-BR-3 cells) were harvested and qRT-PCR was performed to detect the YB1 mRNA levels.SK-BR-3 cells were stimulated with various concentrations of PDGF-BB and YB1 expression levels were detected by qRT-PCR. Down-regulation or over-expression of YB1 by si-YB1 or Ad-GFP-YB1 was detected in SK-BR-3 cells. And MTS cell proliferation assay kit was used to detect cell proliferation.

RESULTS

YB1 mRNA levels were significantly higher in breast cancer tissues and MDA-MB-231 and SK-BR-3 breast cancer cell lines than that in adjacent normal breast tissues and HBL-100 mammary epithelial cells respectively (P < 0.05).YB1 expression levels increased in PDGF-BB stimulated SK-BR-3 cells in a dose-dependent manner.

CONCLUSION

A down-regulation of endogenous YB1 decreases and an over-expression of exogenous YB1 promotes the proliferation activity in SK-BR-3 cells.

摘要

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