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丝氨酸/苏氨酸激酶15基因多态性与消化系统癌症风险:一项荟萃分析。

Serine/threonine kinase 15 gene polymorphism and risk of digestive system cancers: A meta-analysis.

作者信息

Luo Jianfei, Yan Ruicheng, Zou Li

机构信息

Department of Gastrointestinal Surgery, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.

出版信息

Exp Ther Med. 2015 Jan;9(1):219-226. doi: 10.3892/etm.2014.2070. Epub 2014 Nov 14.

Abstract

Previous studies have reported an association between the two coding polymorphisms (91T>A and 169G>A) of the serine/threonine kinase 15 (STK15) gene and the risk of digestive system cancers; however, the results are inconsistent. In the present study, a meta-analysis was carried out to assess the association between the two STK15 polymorphisms and the risk of digestive system cancers. Relevant studies were identified using PubMed, Web of Science, China National Knowledge Infrastructure, WanFang and VIP databases up to February 18, 2014. The pooled odds ratio (OR) with a 95% confidence interval (CI) was calculated using the fixed or random effects model. A total of 15 case-control studies from 14 publications were included. Of these, 15 studies concerned the 91T>A polymorphism and included 7,619 cases and 7,196 controls and four studies concerned the 161G>A polymorphism and included 826 cases and 713 controls. A significantly increased risk of digestive system cancers was observed for the 91T>A polymorphism (recessive model: OR, 1.19; 95% CI, 1.07-1.31). In subgroup analysis by ethnicity, a significant association was detected in Asian populations (recessive model: OR, 1.21; 95% CI, 1.08-1.36) but not in Caucasian and mixed populations. Stratification by tumor type indicated that the 91T>A polymorphism was associated with an increased risk of esophageal and colorectal cancers under the recessive model (OR, 1.19; 95% CI, 1.03-1.38; and OR, 1.24; 95% CI, 1.04-1.46; respectively); however, no significant association was observed between the 169G>A polymorphism and the risk of digestive system cancers in any of the genetic models. Furthermore, in subgroup analysis by ethnicity, similar results were observed in the Asian and Caucasian populations. The present meta-analysis demonstrated that the STK15 gene 91T>A polymorphism, but not the 169G>A polymorphism, may be a risk factor for digestive system cancers, particularly for esophageal and colorectal cancers.

摘要

既往研究报道了丝氨酸/苏氨酸激酶15(STK15)基因的两个编码多态性(91T>A和169G>A)与消化系统癌症风险之间的关联;然而,结果并不一致。在本研究中,进行了一项荟萃分析以评估STK15基因的这两个多态性与消化系统癌症风险之间的关联。利用PubMed、Web of Science、中国知网、万方和维普数据库检索截至2014年2月18日的相关研究。采用固定效应模型或随机效应模型计算合并比值比(OR)及95%置信区间(CI)。共纳入来自14篇文献的15项病例对照研究。其中,15项研究涉及91T>A多态性,包括7619例病例和7196例对照;4项研究涉及161G>A多态性,包括826例病例和713例对照。对于91T>A多态性,观察到消化系统癌症风险显著增加(隐性模型:OR,1.19;95%CI,1.07 - 1.31)。在按种族进行的亚组分析中,在亚洲人群中检测到显著关联(隐性模型:OR,1.21;95%CI,1.08 - 1.36),但在白种人和混合人群中未检测到。按肿瘤类型分层表明,在隐性模型下,91T>A多态性与食管癌和结直肠癌风险增加相关(OR分别为1.19;95%CI,1.03 - 1.38;以及OR,1.24;95%CI,1.04 - 1.46);然而,在任何遗传模型中,均未观察到169G>A多态性与消化系统癌症风险之间存在显著关联。此外,在按种族进行的亚组分析中,在亚洲和白种人群中观察到了类似结果。本荟萃分析表明,STK15基因的91T>A多态性而非169G>A多态性可能是消化系统癌症的一个风险因素,尤其是食管癌和结直肠癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7294/4247321/7e55de61de60/ETM-09-01-0219-g00.jpg

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