Department of Urological Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, China.
DNA Cell Biol. 2012 Jul;31(7):1187-97. doi: 10.1089/dna.2011.1567. Epub 2012 Feb 17.
Glutathione S-transferase T1 (GSTT1) is implicated in the inactivation of procarcinogens that contribute to cancer progression. However, studies investigating the association between GSTT1 polymorphism and bladder cancer (BC) risk have reported conflicting results; therefore, a meta-analysis was conducted. Fifty studies with 10,805 cases and 13,332 controls were recruited. The overall odds ratio for the GSTT1 null genotype was 1.1502 (95% CI=1.0384-1.2741). When stratified by ethnicity, significantly increased risk was only found for Caucasians. In Asians subgroup, interestingly, decreased BC risks were found in the Korean and Japanese populations but not in the Chinese population. When stratified by control sources, a slightly elevated risk was found in population-based but not in hospital-based studies. Besides, smoking was not found to modify the association between the GSTT1 null genotype and BC risk. When combined with the GSTM1 null genotype, a remarkably increased risk was found for BC. In general, our results suggest that the GSTT1 null genotype is associated with an increased risk of BC. Smoking did not modify the association between the GSTT1 null genotype and BC risk. Furthermore, a strong association was observed between the combination of GSTT1 null and GSTM1 null genotype and risk of BC. Further epidemiological studies will be needed to confirm our findings.
谷胱甘肽 S-转移酶 T1(GSTT1)参与了前致癌物的失活,这些前致癌物有助于癌症的进展。然而,研究 GSTT1 多态性与膀胱癌(BC)风险之间的关联的结果相互矛盾;因此,进行了荟萃分析。共纳入 50 项研究,包括 10805 例病例和 13332 例对照。GSTT1 缺失基因型的总体优势比为 1.1502(95%CI=1.0384-1.2741)。按种族分层,仅在白种人中发现风险显著增加。有趣的是,在亚洲人群亚组中,韩国和日本人群的 BC 风险降低,但中国人群没有。按对照来源分层,在基于人群的研究中发现风险略有升高,但在基于医院的研究中没有发现。此外,吸烟未改变 GSTT1 缺失基因型与 BC 风险之间的关联。当与 GSTM1 缺失基因型结合时,BC 的风险显著增加。总体而言,我们的结果表明 GSTT1 缺失基因型与 BC 的风险增加相关。吸烟并未改变 GSTT1 缺失基因型与 BC 风险之间的关联。此外,GSTT1 缺失和 GSTM1 缺失基因型的组合与 BC 的风险之间存在很强的关联。需要进一步的流行病学研究来证实我们的发现。