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      Non-Coding Polymorphisms in Nucleotide Binding Domain 1 in ABCC1 Gene Associate with Transcript Level and Survival of Patients with Breast Cancer

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          Abstract

          Objectives

          ATP-Binding Cassette (ABC) transporters may cause treatment failure by transporting of anticancer drugs outside of the tumor cells. Multidrug resistance-associated protein 1 coded by the ABCC1 gene has recently been suggested as a potential prognostic marker in breast cancer patients. This study aimed to explore tagged haplotype covering nucleotide binding domain 1 of ABCC1 in relation with corresponding transcript levels in tissues and clinical phenotype of breast cancer patients.

          Methods

          The distribution of twelve ABCC1 polymorphisms was assessed by direct sequencing in peripheral blood DNA (n = 540).

          Results

          Tumors from carriers of the wild type genotype in rs35623 or rs35628 exhibited significantly lower levels of ABCC1 transcript than those from carriers of the minor allele (p = 0.003 and p = 0.004, respectively). The ABCC1 transcript levels significantly increased in the order CT-GT>CC-GT>CC-GG for the predicted rs35626-rs4148351 diplotype. Chemotherapy-treated patients carrying the T allele in rs4148353 had longer disease-free survival than those with the GG genotype (p = 0.043). On the other hand, hormonal therapy-treated patients with the AA genotype in rs35628 had significantly longer disease-free survival than carriers of the G allele (p = 0.012).

          Conclusions

          Taken together, our study shows that genetic variability in the nucleotide binding domain 1 has a significant impact on the ABCC1 transcript level in the target tissue and may modify survival of breast cancer patients.

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          Most cited references33

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          Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line.

          The doxorubicin-selected lung cancer cell line H69AR is resistant to many chemotherapeutic agents. However, like most tumor samples from individuals with this disease, it does not overexpress P-glycoprotein, a transmembrane transport protein that is dependent on adenosine triphosphate (ATP) and is associated with multidrug resistance. Complementary DNA (cDNA) clones corresponding to messenger RNAs (mRNAs) overexpressed in H69AR cells were isolated. One cDNA hybridized to an mRNA of 7.8 to 8.2 kilobases that was 100- to 200-fold more expressed in H69AR cells relative to drug-sensitive parental H69 cells. Overexpression was associated with amplification of the cognate gene located on chromosome 16 at band p13.1. Reversion to drug sensitivity was associated with loss of gene amplification and a marked decrease in mRNA expression. The mRNA encodes a member of the ATP-binding cassette transmembrane transporter superfamily.
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            Overcoming multidrug resistance in cancer: an update on the clinical strategy of inhibiting p-glycoprotein.

            Multidrug resistance (MDR) is a significant obstacle to providing effective chemotherapy to many patients. Multifactorial in etiology, classic MDR is associated with the overexpression of P-glycoprotein (P-gp), resulting in increased efflux of chemotherapy from cancer cells. Inhibiting P-gp as a method to reverse MDR in cancer patients has been studied extensively, but the results have generally been disappointing. The development of P-gp inhibitors is reviewed, including a discussion of early agents that are no longer being developed and third-generation agents that are currently in clinical trials. First-generation agents (eg, cyclosporin, verapamil) were limited by unacceptable toxicity, whereas second-generation agents (eg, valspodar, biricodar) had better tolerability but were confounded by unpredictable pharmacokinetic interactions and interactions with other transporter proteins. Third-generation inhibitors (tariquidar XR9576, zosuquidar LY335979, laniquidar R101933, and ONT-093) have high potency and specificity for P-gp. Furthermore, pharmacokinetic studies to date have shown no appreciable impact on cytochrome P450 3A4 drug metabolism and no clinically significant drug interactions with common chemotherapy agents. Third-generation P-gp inhibitors have shown promise in clinical trials. The continued development of these agents may establish the true therapeutic potential of P-gp-mediated MDR reversal.
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              Predicting drug sensitivity and resistance: profiling ABC transporter genes in cancer cells.

              For analysis of multidrug resistance, a major barrier to effective cancer chemotherapy, we profiled mRNA expression of the 48 known human ABC transporters in 60 diverse cancer cell lines (the NCI-60) used by the National Cancer Institute to screen for anticancer activity. The use of real-time RT-PCR avoided artifacts commonly encountered with microarray technologies. By correlating the results with the growth inhibitory profiles of 1,429 candidate anticancer drugs tested against the cells, we identified which transporters are more likely than others to confer resistance to which agents. Unexpectedly, we also found and validated compounds whose activity is potentiated, rather than antagonized, by the MDR1 multidrug transporter. Such compounds may serve as leads for development.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                31 July 2014
                : 9
                : 7
                : e101740
                Affiliations
                [1 ]Department of Toxicogenomics, National Institute of Public Health, Prague, Czech Republic
                [2 ]3rd Faculty of Medicine, Charles University, Prague, Czech Republic
                [3 ]Department of Oncology, Palacky University Medical School and Teaching Hospital, Olomouc, Czech Republic
                [4 ]Institute for the Care for Mother and Child, Prague, Czech Republic
                [5 ]Biolab Praha, k.s., Prague, Czech Republic
                [6 ]Department of Oncology, Motol University Hospital, Prague, Czech Republic
                [7 ]Department of Radiotherapy and Oncology, Faculty Hospital Kralovske Vinohrady, Prague, Czech Republic
                [8 ]Institute of Experimental Medicine, Czech Academy of Sciences, Prague, Czech Republic
                [9 ]Institute of Biology and Medical Genetics, 1st Faculty of Medicine, Charles University, Prague, Czech Republic
                Sudbury Regional Hospital, Canada
                Author notes

                Competing Interests: Dr. Marketa Trnková is employed by a commercial company (Biolab Praha, k.s.). This does not alter the authors’ adherence to PLOS ONE policies on sharing data and materials.

                Conceived and designed the experiments: RV DV VP PS. Performed the experiments: TK VH RV. Analyzed the data: TK KR MT KK MA LV PS. Contributed reagents/materials/analysis tools: VP KR MT KK MA LV PV. Wrote the paper: TK RV VH DV PV PS.

                Article
                PONE-D-14-06671
                10.1371/journal.pone.0101740
                4117604
                25078270
                5a537050-32f1-42b1-beea-0dcc237da834
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 12 February 2014
                : 10 June 2014
                Page count
                Pages: 13
                Funding
                This work was supported by grant of the Internal Grant Agency of the Czech Ministry of Health ( www.mzcr.cz), no.: NT13679-4 and by the project of the Czech Science Foundation no.: P303/12/G163 ( www.gacr.cz). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Biolab Praha, k.s provided support in the form of salary for author MT, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific role of this author is articulated in the ‘author contributions’ section.
                Categories
                Research Article
                Medicine and Health Sciences
                Clinical Genetics
                Personalized Medicine
                Clinical Medicine
                Oncology
                Cancers and Neoplasms
                Breast Tumors
                Invasive Ductal Carcinoma
                Cancer Treatment
                Endocrine Therapy
                Pharmacology
                Pharmacogenetics

                Uncategorized
                Uncategorized

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