Jiang Hua-Yong, Zeng Yong, Xu Wei-Dong, Liu Chuan, Wang Ya-Jie, Wang Ya-Di, Wang Ya-Di
Department of Radiation Oncology,General Hospital of Beijing Military Command, Beijing, China E-mail :
Asian Pac J Cancer Prev. 2015;16(9):3645-51. doi: 10.7314/apjcp.2015.16.9.3645.
Previous studies evaluating the association between the xeroderma pigmentosum group G (XPG) Asp1104His polymorphism and head and neck cancer susceptibility have proven controversial. This meta-analysis of the literature was performed to obtain a more precise estimation of the relationship.
We systematically searched PubMed, Embase and Web of Science with a time limit of Dec 18, 2014. Odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of any association.
We performed a meta-analysis of eight published case-control studies, including 3,621 cases and 5,475 controls. Overall, no significant association was found between the XPG Asp1104His polymorphism and head and neck cancer susceptibility under all genetic models. In the subgroup analysis by ethnicity, the XPG Asp1104His polymorphism had statistically significant association with elevated head and neck cancer risk under CC vs GG (OR=1.24, 95% CI=1.001.54) and the recessive model (OR=1.22, 95%CI=1.011.46) in Asian populations. A similar result was found under CC vs GG (OR =1.22, 95%CI =1.011.47) in the population based subgroup by source of control. When performed by tumor site, the XPG Asp1104His polymorphism had statistically significant association with elevated laryngeal cancer under all genetic models (CC vs GG: OR=1.59, 95% CI=1.162.19; GC vs GG: OR=1.38, 95%CI=1.101.72; dominant model: OR=1.42, 95% CI=1.151.74; recessive model: OR=1.36, 95% CI=1.02~1.81).
This meta-analysis suggested that the XPG Asp1104His polymorphism is a risk factor for head and neck cancer susceptibility, especially for laryngeal cancer and in Asian populations.
先前评估着色性干皮病G组(XPG)Asp1104His多态性与头颈癌易感性之间关联的研究结果存在争议。进行此项文献荟萃分析以更精确地评估二者关系。
我们系统检索了截至2014年12月18日的PubMed、Embase和科学网。采用比值比(OR)及95%置信区间(CI)评估关联强度。
我们对八项已发表的病例对照研究进行了荟萃分析,包括3621例病例和5475例对照。总体而言,在所有遗传模型下,未发现XPG Asp1104His多态性与头颈癌易感性之间存在显著关联。在按种族进行的亚组分析中,在亚洲人群中,XPG Asp1104His多态性在CC与GG比较(OR = 1.24,95% CI = 1.001.54)及隐性模型(OR = 1.22,95% CI = 1.011.46)下与头颈癌风险升高具有统计学显著关联。在按对照来源进行的基于人群的亚组分析中,CC与GG比较时也发现了类似结果(OR = 1.22,95% CI = 1.011.47)。按肿瘤部位分析时,在所有遗传模型下,XPG Asp1104His多态性与喉癌风险升高具有统计学显著关联(CC与GG比较:OR = 1.59,95% CI = 1.162.19;GC与GG比较:OR = 1.38,95% CI = 1.101.72;显性模型:OR = 1.42,95% CI = 1.151.74;隐性模型:OR = 1.36,95% CI = 1.02~1.81)。
此项荟萃分析表明,XPG Asp1104His多态性是头颈癌易感性的一个风险因素,尤其是对于喉癌以及在亚洲人群中。