Hu Yanliang, Sun Zhifang, Zhang Anhua, Zhang Jinjie
Department of General Surgery, People's Hospital of Gaomi Municipality, 77 Zhenfu Road, Gaomi, 261500, Shandong, China,
Tumour Biol. 2014 Jan;35(1):695-9. doi: 10.1007/s13277-013-1095-2. Epub 2013 Aug 16.
Mothers against decapentaplegic homolog 7 (SMAD7) rs12953717 polymorphism has been implicated to alter the risk of colorectal cancer (CRC), but the results are controversial. The objective of this study was to quantitatively evaluate the association between SMAD7 rs12953717 polymorphism and CRC susceptibility. A comprehensive search was conducted to identify all eligible studies of SMAD7 rs12953717 polymorphism and CRC risk. Pooled odds ratio and 95% confidence interval were calculated using a fixed or random effects model. Statistical analysis was performed with Review Manager 5.0 and Stata 11. A total of 11 case-control studies, including 12,058 cases and 11,444 controls, were identified. The combined results based on all studies suggested that rs12953717 was associated with CRC risk under all genetic models. When stratifying for race, the data showed that the rs12953717 was associated with a significantly increased CRC risk under all genetic models in Caucasians. Statistically significant association was found in all genetic models except in recessive model comparison in the subgroup of Asians. After stratifying the studies by study design, there was a significant association between rs12953717 polymorphism and CRC risk under all genetic models in the subgroup of population-based studies. Our study suggests that rs12953717 polymorphism is associated with an increased CRC risk.
抗十号染色体缺失同源物7(SMAD7)基因rs12953717多态性被认为与结直肠癌(CRC)风险改变有关,但结果存在争议。本研究的目的是定量评估SMAD7基因rs12953717多态性与CRC易感性之间的关联。进行了全面检索以识别所有关于SMAD7基因rs12953717多态性与CRC风险的合格研究。使用固定效应或随机效应模型计算合并比值比和95%置信区间。使用Review Manager 5.0和Stata 11进行统计分析。共纳入11项病例对照研究,包括12058例病例和11444例对照。基于所有研究的合并结果表明,在所有遗传模型下,rs12953717与CRC风险相关。按种族分层时,数据显示在所有遗传模型下,rs12953717在白种人中与CRC风险显著增加相关。在亚洲人亚组的隐性模型比较中除外,在所有遗传模型中均发现有统计学意义的关联。按研究设计对研究进行分层后,在基于人群研究的亚组中,rs12953717多态性与CRC风险在所有遗传模型下均存在显著关联。我们的研究表明,rs12953717多态性与CRC风险增加相关。