1. Differentially expressed proteins in human MCF-7 breast cancer cells sensitive and resistant to paclitaxel.
- Author
-
Pavlíková N, Bartoňová I, Balušíková K, Kopperova D, Halada P, and Kovář J
- Subjects
- ATPases Associated with Diverse Cellular Activities, Adaptor Proteins, Signal Transducing metabolism, Breast Neoplasms, Cathepsin D metabolism, Drug Resistance, Neoplasm, Female, HSP27 Heat-Shock Proteins metabolism, Heat-Shock Proteins, Humans, LIM Domain Proteins metabolism, MCF-7 Cells, Molecular Chaperones, Proteasome Endopeptidase Complex, Transcription Factors metabolism, Antineoplastic Agents, Phytogenic pharmacology, Paclitaxel pharmacology, Proteome metabolism
- Abstract
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., (Copyright © 2014 Elsevier Inc. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF