Cai Qiliang, Wu Tao, Zhang Wei, Guo Xuemei, Shang Zhiqun, Jiang Ning, Tian Jing, Niu Yuanjie
Department of Urology, The Second Hospital of Tianjin Medical University, Tianjin Institute of Urology, Tianjin, 300211, China.
Tumour Biol. 2013 Dec;34(6):3913-22. doi: 10.1007/s13277-013-0979-5. Epub 2013 Jul 11.
Numerous epidemiological studies have evaluated the association between the glutathione S-transferases P1 (GSTP1) Ile105Val polymorphisms and prostate cancer (PCa) risk. However, these studies have yielded conflicting results. A comprehensive search was conducted through researching MEDLINE, PubMed, Web of Science, and EMBASE, and a total of 13 studies including 3,227 cases and 3,945 controls were identified. A meta-analysis was performed to obtain a summary of estimated odds ratios (ORs) and 95% confidence intervals (CIs) of GSTP1 polymorphisms for PCa, with attention to study quality and publication bias. The GSTP1 Ile158Val variant genotypes are less associated with increased risk of PCa for the homozygote model (Val/Val vs Ile/Ile: OR = 1.42; I(2) = 63.7%; 95% CI = 1.02-1.97) and the recessive model (OR = 1.41; I(2) = 45.5%; 95% CI = 1.10-1.80). However, no associations were detected for other genetic models. In the stratified analysis by ethnicity, significant associations between GSTP1 Ile105Val polymorphism and PCa risk were also found among Caucasians for Val/Val vs Ile/Ile comparison (OR = 1.22; I(2) = 0.0 %; 95 % CI = 1.02-1.47) and for the recessive model (OR = 1.26; I(2) = 0.0%; 95% CI = 1.06-1.49), while there were no associations found for other genetic models. However, no associations were found in Asians and African-Americans for all genetic models when stratified by ethnicity. In conclusion, our meta-analysis provides evidence that GSTP1 Ile105Val gene polymorphisms contributed to PCa susceptibility.
众多流行病学研究评估了谷胱甘肽S-转移酶P1(GSTP1)Ile105Val基因多态性与前列腺癌(PCa)风险之间的关联。然而,这些研究结果相互矛盾。通过检索MEDLINE、PubMed、科学网和EMBASE进行了全面搜索,共识别出13项研究,包括3227例病例和3945例对照。进行了一项荟萃分析,以获取GSTP1基因多态性与PCa相关的估计比值比(OR)和95%置信区间(CI)的汇总信息,同时关注研究质量和发表偏倚。对于纯合子模型(Val/Val与Ile/Ile比较:OR = 1.42;I² = 63.7%;95% CI = 1.02 - 1.97)和隐性模型(OR = 1.41;I² = 45.5%;95% CI = 1.10 - 1.80),GSTP1 Ile158Val变异基因型与PCa风险增加的关联较小。然而,未检测到其他遗传模型存在关联。在按种族进行的分层分析中,在白种人中,对于Val/Val与Ile/Ile比较(OR = 1.22;I² = 0.0%;95% CI = 1.02 - 1.47)和隐性模型(OR = 1.26;I² = 0.0%;95% CI = 1.06 - 1.49),也发现GSTP1 Ile105Val基因多态性与PCa风险之间存在显著关联,而对于其他遗传模型未发现关联。然而,按种族分层时,在亚洲人和非裔美国人中,所有遗传模型均未发现关联。总之,我们的荟萃分析提供了证据表明GSTP1 Ile105Val基因多态性与PCa易感性有关。