A microarray based expression profiling of paclitaxel and vincristine resistant MCF-7 cells

Date

2011-04-25

Author

DEMİREL KARS, MELTEM
Iseri, Ozlem Darcansoy
Gündüz, Ufuk

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Resistance to the broad spectrum of chemotherapeutic agents in cancer cell lines and tumors has been called multiple drug resistance (MDR). In this study, the molecular mechanisms of resistance to two anticancer agents (paclitaxel and vincristine) in mammary carcinoma cell line MCF-7 were investigated. Drug resistant sublines to paclitaxel (MCF-7/Pac) and vincristine (MCF-7/Vinc) that were developed from sensitive MCF-7 cells (MCF-7/S) were used. cDNA microarray analysis was performed for the RNA samples of sensitive and resistant cells in duplicate experiments. GeneSpring GX 7.3.1 Software was used in data analysis. The results indicated that the upregulation of MDR] gene is the dominating mechanism of the paclitaxel and vincristine drug resistance. Additionally the upregulation of the genes encoding the detoxifying enzymes (i.e. GSTP1) was observed. Significant downregulation of apoptotic genes (i.e. PDCD2/4/6/8) and upregulation of some cell cycle regulatory genes (CDKN2A, CCNA2 etc.) was seen which may be in close relation to MDR in breast cancer. Drug resistant cancer cells exhibit different gene expression patterns depending on drug treatment, and each drug resistance phenotype is probably genetically different. Further functional studies are needed to demonstrate the complete set of genes contributing to the drug resistance phenotype in breast cancer cells.

Subject Keywords

MCF-7, Multiple drug resistance, Microarray analysis, Vincristine

URI

https://hdl.handle.net/11511/31694

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY

DOI

https://doi.org/10.1016/j.ejphar.2011.02.001

Collections

Graduate School of Natural and Applied Sciences, Article

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Citation Formats

M. DEMİREL KARS, O. D. Iseri, and U. Gündüz, “A microarray based expression profiling of paclitaxel and vincristine resistant MCF-7 cells,” EUROPEAN JOURNAL OF PHARMACOLOGY, pp. 4–9, 2011, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/31694.