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Article type: Research Article
Authors: Zatelli, Maria Chiara | Molè, Daniela | Tagliati, Federico | Minoia, Mariella | Ambrosio, Maria Rosaria | Uberti, Ettore degli
Affiliations: Section of Endocrinology, Department of Biomedical Sciences and Advanced Therapies, University of Ferrara, Ferrara, Italy
Note: [] Corresponding author: Prof. Ettore C. degli Uberti, Section of Endocrinology, Department of Biomedical Sciences and Advanced Therapies, University of Ferrara, Via Savonarola 9, 44100 Ferrara, Italy. Tel.: +39 0532 236682; Fax: +39 0532 236514; E-mail: ti8@unife.it.
Abstract: Background: Breast cancer cells can develop chemoresistance after prolonged exposure to cytotoxic drugs due to expression of the multi drug resistance (MDR) 1 gene. Type 2 cyclo-oxygenase (COX-2) inhibitors reverse the chemoresistance phenotype of a medullary thyroid carcinoma cell line, TT, and of a breast cancer cell line, MCF7, by inhibiting MDR1 expression and P-gp function. Aim: investigate the role of prostaglandin (PG) in modulating chemoresistance in MCF7 cells and to explore the involved intracellular mechanisms. Methods: native and chemoresistant MCF7 cells were treated with PGH2 and resistance to Doxorubicin was tested in the presence or absence of COX-2 inhibitors. Results: PGH2 restores resistance to the cytotoxic effects of Doxo, with concomitant nuclear translocation of the transcription factor NF-κB. Conclusions: COX-2 inhibitors prevent chemoresistance development in breast cancer cells by inhibiting P-gp expression and function by a mechanism that involves PGH2 generation and NF-κB activation.
Keywords: PGH_2, P-gp, COX-2 inhibitors, NF-κB, chemoresistance, breast cancer
DOI: 10.3233/CLO-2009-0490
Journal: Analytical Cellular Pathology, vol. 31, no. 6, pp. 457-465, 2009
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