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机构地区:[1]岳阳职业技术学院医学基础部,湖南岳阳414000
出 处:《肿瘤药学》2013年第5期340-343,352,共5页Anti-Tumor Pharmacy
基 金:湖南省教育厅基金资助项目(11C1284)
摘 要:目的探讨PTEN在乳腺癌对顺铂化疗敏感性中的作用及其可能的机制。方法应用脂质体转染技术建立PTEN沉默的乳腺癌细胞系MCF-7/PTENi,通过MTT实验检测其对顺铂的敏感性,并通过Western印迹法检测细胞中Bcl-2的表达水平;应用小分子抑制剂ABT-737抑制Bcl-2表达后,再次检测MCF-7/PTENi对顺铂的敏感性。结果 MCF-7/PTENi和阴性对照细胞(MCF-7/NC)对顺铂的IC50值分别为(16.01±3.03)和(7.86±0.85)μM,两者差异有统计学意义(P=0.003)。MCF-7/PTENi细胞中Bcl-2的表达水平明显高于MCF-7/NC细胞(P=0.015)。2μM ABT-737处理的MCF-7/PTENi和MCF-7/NC细胞对顺铂的IC50值比较无显著性差异(P=0.087)。结论 PTEN沉默可降低乳腺癌细胞对顺铂的敏感性,其机制可能与其增加Bcl-2的表达有关。Objective To study the roles of PTEN in the cisplatin chemosensitivity of breast cancer and its possible mecha-nisms. Methods PTEN-silenced MCF-7 cell line (MCF-7/PTENi) was established by lipofectamine transfection. The sensitiv-ity of MCF-7/PTENi cells to cisplatin was tested by MTT treated with or without ABT-737, a novel small molecule inhibitor of Bcl-2 protein. The expression of Bcl-2 was detected by Western blotting. Results The IC50 of MCF-7/PTENi cells treated by cisplatin was 16.01±3.03μM, and it was significantly higher than that of MCF-7/NC cells which was 7.86±0.85μM, with statistical difference (P=0.003). The expression of Bcl-2 in MCF-7/PTENi cells was significantly higher than that of MCF-7/NC cells (P=0.015). No significant difference was found between the MCF-7/PTENi and MCF-7/NC cells treated with 2μM ABT-737 and cisplatin (P=0.087). Conclusion Loss of PTEN expression decreased the chemosensitivity of breast cancer cells to cisplatin, and its mechanism may be involved with the increase of Bcl-2 expression.
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