作者
Aneta Mirecka, Katarzyna Paszkowska-Szczur, Rodney J Scott, Bohdan Górski, Thierry van de Wetering, Dominika Wokołorczyk, Tomasz Gromowski, Pablo Serrano-Fernandez, Cezary Cybulski, Aniruddh Kashyap, Satish Gupta, Adam Gołąb, Marcin Słojewski, Andrzej Sikorski, Jan Lubiński, Tadeusz Dębniak
发表日期
2014/8/10
期刊
Gene
卷号
546
期号
2
页码范围
156-161
出版商
Elsevier
简介
The genetic basis of prostate cancer (PC) is complex and appears to involve multiple susceptibility genes. A number of studies have evaluated a possible correlation between several NER gene polymorphisms and PC risk, but most of them evaluated only single SNPs among XP genes and the results remain inconsistent. Out of 94 SNPs located in seven XP genes (XPAXPG) a total of 15 SNPs were assayed in 720 unselected patients with PC and compared to 1121 healthy adults. An increased risk of disease was associated with the XPD SNP, rs1799793 (Asp312Asn) AG genotype (OR = 2.60; p < 0.001) and with the AA genotype (OR = 531; p < 0.0001) compared to the control population. Haplotype analysis of XPD revealed one protective haplotype and four associated with an increased disease risk, which showed that the A allele (XPD rs1799793) appeared to drive the main effect on promoting prostate cancer …
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