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乳腺癌中STAT3对HSP27和cMYC表达的调控作用
http://www.100md.com 《第四军医大学学报》 2006年第2期
乳腺癌,,乳腺肿瘤;癌基因;信号转导和转录激活因子3;热休克蛋白27;基因,cMYC,0引言,1材料和方法,2结果,3讨论,【参考文献
     Regulating role of STAT3 to HSP27 and cMYC expression in breast cancer

    SUN ZhengKui, YAO ZhenXiang, LIU ShengChun

    Department of General Surgery, First Affiliated Hospital, Chongqing University of Medical Sciences, Chongqing 400016, China

    【Abstract】 AIM: To investigate the regulating role of signal transducer and activator of transcription 3 (STAT3) to 27 ku heat shock protein (HSP27) and cMYC expression in breast cancer. METHODS: Expressions of STAT3, HSP27 and cMYC were examined in primary breast infiltrating duct carcinoma tissues of 51 patients using immunohistochemistry. Correlations between STAT3 expression and HSP27 or cMYC expression were analyzed with statistic method. After the transfection of MDAMB435S human breast carcinoma cells with STAT3 decoy oligodeoxynucleotides (Decoy ODNs), expressions of HSP27 and cMYC of MDAMB435S were semiquantified by Western blot, the apoptosis and the cell cycle distribution of MDAMB435S cells were analyzed with flow cytometry and proliferation of MDAMB435S cells was analyzed by MTT assay. RESULTS: In primary breast infiltrating duct carcinoma tissues, STAT3 expression was correlated positively with HSP27 expression and cMYC expression respectively (rs=0.454, P=0.001; rs=0.541, P=0.000). As the result of STAT3 inhibition by STAT3 Decoy ODNs in MDAMB435S cells, expressions of HSP27 and cMYC were markedly reduced, which was consistent with STAT3 activation reduction (Both P<0.01). The cell cycle progression of MDAMB435S cells was significantly inhibited at G0/G1 phase, the apoptosis of those cells was augmented and their proliferation was inhibited (P<0.01). CONCLUSION: Constitutively activated STAT3 may upregulate HSP27 and cMYC expression to inhibit breast cancer cell apoptosis and to facilitate their proliferation, thus leading to the malignancy of breast cancer cells. ......

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