Survivin transcription is associated with P-glycoprotein/MDR1 overexpression in the multidrug resistance of MCF-7 breast cancer cells

被引:57
作者
Liu, Feng
Liu, Shiying
He, Shengnan [3 ]
Xie, Zhenhua
Zu, Xuyu
Jiang, Yuyang [1 ,2 ]
机构
[1] Tsinghua Univ, Dept Life Sci, Grad Sch Shenzhen, Key Lab Chem Biol, Shenzhen 518055, Guangdong Prov, Peoples R China
[2] Tsinghua Univ, Sch Med, Beijing 100084, Peoples R China
[3] Shenyang Pharmaceut Univ, Shenzhen 110016, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
survivin; multidrug resistance; P-glycoprotein; MCE-7; PI3k/Akt; P-GLYCOPROTEIN; GENE-EXPRESSION; ENDOTHELIAL-CELLS; APOPTOSIS; SENSITIVITY; ACTIVATION; PATHWAY; TUMORS; INHIBITOR; PROMOTER;
D O I
10.3892/or_00000786
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast carcinoma is the most common malignancy in women. The progression of tumor is associated with overexpression of inhibitors of apoptosis proteins (IAPs) such as survivin and multidrug resistant P-glycoprotein (P-gp). PI3K/Akt pathway is involved in cell cycle progression, apoptosis and neoplastic transformation. PI3K/Akt has been shown to regulate survivin in breast cancer. The aim of this study was to investigate the expression of survivin and P-gp, the modulation of survivin by P-gp in PI3K/Akt during the progression of drug resistance (MDR) in MCF-7 breast cancer cells and adriamycin (ADR)-resistant MCF-7/ADR cells. The expression of survivin and P-gp in MCF-7/ADR cells were higher than that of the MCF-7 cells using RT-PCR and Western blot analysis. Survivin transcription was associated with P-glycoprotein/MDR1 overexpression using promoter activity analysis. LY294002, specific inhibitor of PI3K could suppress survivin and P-gp expression, decreased survivin promoter activity and enhanced cell sensitivity to drugs. This study shows survivin transcription was associated with P-glycoprotein/MDR1 overexpression, PI3k/Akt pathway was involved in P-glycoprotein/MDR1 associated survivin transcription activity in the multidrug resistant MCF-7 breast cancer cells.
引用
收藏
页码:1469 / 1475
页数:7
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