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저자정보
Abuhaliema, Ali M (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan) Yousef, Al-Motassem F (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan) El-Madany, Nirmeen N (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan) Bulatova, Nailya R (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan) Awwad, Nemah M (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan) Yousef, Muhammad A (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan) Al Majdalawi, Khalil Z (Department of Biopharmaceutics and Clinical Pharmacy, Faculty of Pharmacy, the University of Jordan)
저널정보
아시아태평양암예방학회 Asian Pacific journal of cancer prevention : APJCP Asian Pacific journal of cancer prevention : APJCP 제17권 제1호
발행연도
2016.1
수록면
261 - 266 (6page)

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Background: Breast cancer is the leading cause of cancer death among women and the second in humans worldwide. Many published studies have suggested an association between MDR1 polymorphisms and breast cancer risk. Our aim was to study the association between genetic polymorphism of MDR1 at three sites (C3435T, G2677A/T, and C1236T) and their haplotype and the risk of breast cancer in Jordanian females. Materials and Methods: A case-control study involving 150 breast cancer cases and 150 controls was conducted. Controls were age-matched to cases. The polymerase chain reaction/restriction fragment length polymorphism (PCR-RFLP) technique and sequencing were performed to analyse genotypes. Results: The distribution of MDR1 C3435T genotypes differed between cases and controls [cases, CC 45.3%, CT 41.3%, and TT 13.3%; controls, CC 13.4%, CT 43.3%, and TT 30.2%, p < 0.001]. Similarly, the distribution of G2677A/T significantly differed [cases, GG 43.1 %, GT+GA 50.9% and AA+TT 6%; controls, GG 29.6 %, GT+GA 50.9%, and AA+TT 19.4%, p = 0.004]. On the other hand, genotype and allelotype distribution of C1236T was not statistically different between cases and controls (p=0.56 and 0.26, respectively). The CGC haplotype increased the risk to breast cancer by 2.5-fold compared to others, while TGC and TTC haplotypes carried 2.5- and 5-fold lower risk of breast cancer, respectively. Conclusions: Genetic polymorphisms of MDR1 C3435T and G2677A/T, but not C1236T, are associated with increased risk of breast cancer. In addition, CGC, TGC and TTC haplotypes have different impacts on the risk of breast cancer. Future, larger studies are needed to validate these findings.

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