乳腺癌中STAT3对HSP27和cMYC表达的调控作用
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,cMYC,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 cMYC expression in breast cancerSUN ZhengKui, YAO ZhenXiang, LIU ShengChun
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 cMYC expression in breast cancer. METHODS: Expressions of STAT3, HSP27 and cMYC were examined in primary breast infiltrating duct carcinoma tissues of 51 patients using immunohistochemistry. Correlations between STAT3 expression and HSP27 or cMYC expression were analyzed with statistic method. After the transfection of MDAMB435S human breast carcinoma cells with STAT3 decoy oligodeoxynucleotides (Decoy ODNs), expressions of HSP27 and cMYC of MDAMB435S were semiquantified by Western blot, the apoptosis and the cell cycle distribution of MDAMB435S cells were analyzed with flow cytometry and proliferation of MDAMB435S cells was analyzed by MTT assay. RESULTS: In primary breast infiltrating duct carcinoma tissues, STAT3 expression was correlated positively with HSP27 expression and cMYC 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 MDAMB435S cells, expressions of HSP27 and cMYC were markedly reduced, which was consistent with STAT3 activation reduction (Both P<0.01). The cell cycle progression of MDAMB435S 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 upregulate HSP27 and cMYC 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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