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Article type: Research Article
Authors: Taheri, Mohsen; ; | Mahjoubi, Frouzandeh
Affiliations: Division of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran | Genetics of Non-communicable Diseases Research Center, Zahedan University of Medical Sciences, Zahedan, Iran | Department of Genetics, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran
Note: [] Corresponding author: Frouzandeh Mahjoubi, Division of Medical Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB) Pajoohesh Blvd. Tehran-Karaj Highway, 17th Km, Tehran, Iran. Tel.: +98 21 44580389; Fax: +98 21 44580399; E-mail: frouz@nigeb.ac.ir
Abstract: A major problem in the treatment of breast cancer is the development of resistance to chemotherapeutic agents. Although the role of multidrug resistance 1 (MDR1) and multidrug resistance associated protein 1 (MRP1) in inducing drug resistance in many cancers has been widely investigated the clinical significance of expression of these genes in breast cancer remains unclear and the data is still controversial. We investigated the expression of MDR1 and MRP1 in breast cancer patients as well as the possible correlation between MDR1 and MRP1 and clinical response to chemotherapy. In the present study, MDR1 and MRP1 gene expression were investigated by real time reverse transcription polymerase chain reaction (RT-PCR) assay in 54 breast cancer tumors and in corresponding adjacent normal tissues before neoadjuvant chemotherapy. The expression level of MDR1 and MRP1 were significantly higher in breast tumors than normal breast tissues. Although a significant relationship was found between the MRP1 expression and response to treatment no association was observed between MDR1 expression and response to treatment. MDR1 and MRP1 expression levels have been shown to be independent of tumor size, histological grade and the status of progesterone or estrogen receptor.
Keywords: Multidrug resistance, real time PCR, breast cancer, MDR1, MRP1
DOI: 10.3233/DMA-130985
Journal: Disease Markers, vol. 34, no. 6, pp. 387-393, 2013
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