Differentially expressed proteins in human MCF-7 breast cancer cells sensitive and resistant to paclitaxel

被引:19
|
作者
Pavlikova, Nela [1 ]
Bartonova, Irena [1 ]
Balusikova, Kamila [1 ]
Kopperova, Dana [1 ]
Halada, Petr [2 ]
Kovar, Jan [1 ]
机构
[1] Charles Univ Prague, Fac Med 3, Dept Cell & Mol Biol, Prague, Czech Republic
[2] Acad Sci Czech Republ, Inst Microbiol, Vvi, Lab Mol Struct Characterizat, Prague, Czech Republic
关键词
Breast cancer; Taxane resistance; 2-D electrophoresis; TRIP6; Heat shock protein 27; Cathepsin D; LIM-DOMAIN PROTEIN; ANTICANCER DRUG PACLITAXEL; CATHEPSIN-D; P-GLYCOPROTEIN; REPRESSING SIGNALS; NUCLEAR ISOFORM; CYTOCHROME-C; IN-VITRO; TRIP6; METABOLISM;
D O I
10.1016/j.yexcr.2014.12.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Resistance of cancer cells to chemotherapeutic agents is one of the main causes of treatment failure. In order to detect proteins potentially involved in the mechanism of resistance to taxanes, we assessed differences in protein expression in MCF-7 breast cancer cells that are sensitive to paclitaxel and in the same cells with acquired resistance to paclitaxel (established in our lab). Proteins were separated using two-dimensional electrophoresis. Changes in their expression were determined and proteins with altered expression were identified using mass spectrometry. Changes in their expression were confirmed using western blot analysis. With these techniques, we found three proteins expressed differently in resistant MCF-7 cells, i.e., thyroid hormone-interacting protein 6 (TRIP6; upregulated to 650%), heat shock protein 27 (HSP27; downregulated to 50%) and cathepsin D (downregulated to 28%). Silencing of TRIP6 expression by specific siRNA leads to decreased number of grown resistant MCF-7 cells. In the present study we have pointed at some new directions in the studies of the mechanism of resistance to paclitaxel in breast cancer cells. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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