Xu Yu, Wang Jun, Dong Weiguo
Department of Otolaryngology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China.
Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China.
PLoS One. 2014 Jan 8;9(1):e83851. doi: 10.1371/journal.pone.0083851. eCollection 2014.
Glutathione S-transferase M3 (GSTM3) is an important member of the GSTs that plays a critical role in the development of head and neck cancer (HNC). Several studies have investigated between the GSTM3 A/B polymorphism and risk of HNC, however, the results remain controversial. The aim of this meta-analysis is to evaluate the association between the GSTM3 A/B polymorphism and the risk of HNC.
All eligible case-control studies published up to July 2013 were identified by searching PubMed and Web of Science. The HNC risk associated with the GSTM3 A/B polymorphism was estimated for each study by odds ratios (OR) together with its 95% confidence interval (CI), respectively.
Fourteen studies from ten publications with 2110 patients and 2259 controls were included. Overall, the GSTM3 A/B polymorphism was associated with a decreased risk of HNC using the dominant model, homozygote comparison model and heterozygote comparison model (OR = 0.82, 95%CI: 0.71-0.94; OR = 0.67, 95%CI: 0.49-0.94; and OR = 0.84, 95%CI: 0.73-0.97, respectively); besides, in stratification analyses by ethnicity, similar results were observed in Caucasian populations. Stratification by tumor site indicated that the GSTM3 polymorphism was associated with a decreased risk of laryngeal cancer under recessive model and homozygote comparison (OR = 0.52, 95%CI: 0.30-0.89; and OR = 0.50, 95%CI: 0.29-0.87, respectively); By stratifying source of control, decreased cancer risk was observed in hospital-based population under all genetic models (OR = 0.67, 95%CI: 0.56-0.81 for the dominant model; OR = 0.66, 95%CI: 0.46-0.95 for the recessive model; OR = 0.55, 95%CI: 0.37-0.83 for the homozygote comparison model, and OR = 0.70, 95%CI: 0.58-0.84 for the heterozygote comparison model).
This meta-analysis suggests that the GSTM3 A/B polymorphism may be an important protective factor for HNC, especially of laryngeal cancer and Caucasian populations.
谷胱甘肽S-转移酶M3(GSTM3)是谷胱甘肽S-转移酶家族的重要成员,在头颈癌(HNC)的发生发展中起关键作用。多项研究调查了GSTM3 A/B基因多态性与HNC风险之间的关系,然而,结果仍存在争议。本荟萃分析的目的是评估GSTM3 A/B基因多态性与HNC风险之间的关联。
通过检索PubMed和科学网,确定截至2013年7月发表的所有符合条件的病例对照研究。分别通过比值比(OR)及其95%置信区间(CI)对每项研究中与GSTM3 A/B基因多态性相关的HNC风险进行估计。
纳入了来自10篇出版物的14项研究,共2110例患者和2259例对照。总体而言,使用显性模型、纯合子比较模型和杂合子比较模型时,GSTM3 A/B基因多态性与HNC风险降低相关(OR分别为0.82,95%CI:0.71 - 0.94;OR为0.67,95%CI:0.49 - 0.94;OR为0.84,95%CI:0.73 - 0.97);此外,在按种族进行的分层分析中,在白种人群中观察到了类似结果。按肿瘤部位分层表明,在隐性模型和纯合子比较中,GSTM3基因多态性与喉癌风险降低相关(OR分别为0.52,95%CI:0.30 - 0.89;OR为0.50,95%CI:0.29 - 0.87);通过对对照来源进行分层,在所有遗传模型下,基于医院的人群中观察到癌症风险降低(显性模型的OR为0.67,95%CI:0.56 - 0.81;隐性模型的OR为0.66,95%CI:0.46 - 0.95;纯合子比较模型的OR为0.55,95%CI:0.37 - 0.83;杂合子比较模型的OR为