1. Genetic polymorphisms of the multidrug resistance 1 gene MDR1 and the risk of hepatocellular carcinoma
- Author
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Qiang Gao, Meng Duan, Xin Yang Liu, Jinjing Hu, Jia Fan, Liu-Xiao Yang, Zhi-Chao Wang, Xiaoying Wang, Long-Zi Liu, Jie-Yi Shi, Yong-Na Wu, and Jian Zhou
- Subjects
Oncology ,medicine.medical_specialty ,ATP Binding Cassette Transporter, Subfamily B ,Carcinoma, Hepatocellular ,Genotype ,Biology ,Bioinformatics ,Polymorphism, Single Nucleotide ,Risk Factors ,Internal medicine ,Genetic model ,Epidemiology ,Ethnicity ,medicine ,Humans ,Genetic Predisposition to Disease ,Risk factor ,Allele ,Liver Neoplasms ,General Medicine ,Odds ratio ,medicine.disease ,Drug Resistance, Multiple ,Hepatocellular carcinoma ,Meta-analysis ,Gene polymorphism - Abstract
A possible association between multiple drug resistance 1 gene (MDR1) polymorphisms and the risk of developing hepatocellular carcinoma (HCC) is currently under debate, and evidence from various epidemiological studies has yielded controversial results. To derive a more precise estimation of the association between MDR1 polymorphisms and HCC risk, the present meta-analysis was performed. A total of 8 studies containing 11 cohorts with 4407 cases and 4436 controls were included by systematic literature search of EMBASE, PubMed, Web of Science, and CNKI. All polymorphisms were classified as mutant/wild-type alleles. In particular, the variation type, functional impact, and protein domain location of the polymorphisms were assessed and used as stratified indicators. The pooled odds ratio (OR) with 95 % confidence interval (CI) was calculated to evaluate the association. Overall, our results suggested that the mutant alleles of the MDR1 gene were associated with a significantly increased risk for HCC under all genetic models (allelic model: OR = 1.28, 95 % CI = 1.20–1.36, P
- Published
- 2015
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