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         headline:The ATP7B genetic polymorphisms predict clinical outcome to platinum-based chemotherapy in lung cancer patients
         description:This study aims to investigate the influence of ATP7B genetic polymorphism to platinum-based chemotherapy in Chinese Han lung cancer patients. A total of 338 Chinese Han lung cancer patients were enrolled in this study. All patients underwent at least two cycles of platinum-based chemotherapy. Four tag SNPs of ATP7B (rs1061472, rs9535826, rs7999812, and rs9535828) were selected to evaluate their impacts to platinum-based chemotherapy in these patients. ATP7B rs9535828 and rs9535826 were found to be associated with platinum resistance in Chinese Han lung cancer patients. Patients with A allele in ATP7B rs9535828 presented an increased susceptibility to platinum drugs (OR 1.96, 95 % CI 1.17–3.30, p < 0.01). Patients with G allele in ATP7B rs9535826 had the highest susceptibility to platinum drugs (OR 2.05, 95 % CI 1.19–3.52, p < 0.01). Our findings suggest that ATP7B genetic polymorphisms could affect the therapeutic efficacy of platinum-based chemotherapy, and ATP7B gene might be considered as predictive markers for the efficacy evaluation of platinum-based chemotherapy in Chinese Han lung cancer patients.
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      headline:The ATP7B genetic polymorphisms predict clinical outcome to platinum-based chemotherapy in lung cancer patients
      description:This study aims to investigate the influence of ATP7B genetic polymorphism to platinum-based chemotherapy in Chinese Han lung cancer patients. A total of 338 Chinese Han lung cancer patients were enrolled in this study. All patients underwent at least two cycles of platinum-based chemotherapy. Four tag SNPs of ATP7B (rs1061472, rs9535826, rs7999812, and rs9535828) were selected to evaluate their impacts to platinum-based chemotherapy in these patients. ATP7B rs9535828 and rs9535826 were found to be associated with platinum resistance in Chinese Han lung cancer patients. Patients with A allele in ATP7B rs9535828 presented an increased susceptibility to platinum drugs (OR 1.96, 95 % CI 1.17–3.30, p < 0.01). Patients with G allele in ATP7B rs9535826 had the highest susceptibility to platinum drugs (OR 2.05, 95 % CI 1.19–3.52, p < 0.01). Our findings suggest that ATP7B genetic polymorphisms could affect the therapeutic efficacy of platinum-based chemotherapy, and ATP7B gene might be considered as predictive markers for the efficacy evaluation of platinum-based chemotherapy in Chinese Han lung cancer patients.
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         Cancer Research
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      name:Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:The Affiliated Cancer Hospital of XiangYa School of Medicine, Central South University, Changsha, People’s Republic of China
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      name:Department of Pharmacy, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
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      name:Institute of Clinical Pharmacology, Hunan Key Laboratory of Pharmacogenetics, Central South University, Changsha, People’s Republic of China
      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
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      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
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      name:Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, People’s Republic of China
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