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The Effect of CHEK2 Variant I157T on Cancer Susceptibility: Evidence from a Meta-Analysis

机译:CHEK2变异体I157T对癌症易感性的影响:来自荟萃分析的证据

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Cell cycle checkpoint kinase 2 (CHEK2) is a checkpoint kinase that plays an important role in the DNA damage signaling network. Numerous epidemiological studies have evaluated the association between the CHEK2 I157T variant and cancer susceptibility. However, the results of these studies on the association remain conflicting. The main purpose of this study was to integrate previous results and explore whether the CHEK2 I157T variant is associated with cancer susceptibility. PubMed, Embase (before 2012-10-1), Google Scholar, and CBMdisc were searched for studies on the relationship of the CHEK2 I157T variant and the incidence of cancer. Eligible articles were included for data extraction. The main outcome was the frequency of CHEK2 I157T polymorphisms between cases and controls. Comparison of the distribution of SNP was mainly performed using Review Manager 5.0. The odds ratio (OR) and its 95% confidence interval (95% CI) were used to assess the strength of association. In total, 26,336 cases and 44,219 controls from 18 case-control studies were used in this metaanalysis, and significant associations of the CHEK2 I157T variant with cancer susceptibility were found (OR, 1.39; 95% CI, 1.19-1.63; p < 0.0001), breast cancer (OR = 1.58, 95% CI = 1.42-1.75, p < 0.00001) and colorectal cancer (OR = 1.67, 95% CI = 1.24-2.26, p = 0.0008). We also found an association of the CHEK2 I157T variant with familial cases (OR = 1.85, 95% CI = 1.51-2.26, p < 0.00001). However, the association was not established for other types of cancer (OR = 1.09, 95% CI = 0.75-1.57, p = 0.66). This meta-analysis demonstrates that the CHEK2 I157T variant was an important cancer gene, which increases cancer risk, especially in breast and colorectal cancer in Caucasian, and the bioinformatic analysis showed this change was mainly attributed to the decreased hydrophobicity of CHEK2 157T.
机译:细胞周期检查点激酶2(CHEK2)是在DNA损伤信号传导网络中起重要作用的检查点激酶。许多流行病学研究已经评估了CHEK2 I157T变异体与癌症易感性之间的关联。但是,这些关于联想的研究结果仍然存在矛盾。这项研究的主要目的是整合先前的结果,并探讨CHEK2 I157T变体是否与癌症易感性相关。搜寻PubMed,Embase(2012-10-1之前),Google Scholar和CBMdisc,以研究CHEK2 I157T变体与癌症发生率之间的关系。纳入符合条件的文章以进行数据提取。主要结果是病例与对照之间CHEK2 I157T多态性的频率。 SNP分布的比较主要是使用Review Manager 5.0进行的。使用比值比(OR)及其95%置信区间(95%CI)评估关联强度。这项荟萃分析总共使用了来自18个病例对照研究的26,336例病例和44,219例对照,并且发现CHEK2 I157T变体与癌症易感性之间存在显着关联(OR,1.39; 95%CI,1.19-1.63; p <0.0001) ,乳腺癌(OR = 1.58,95%CI = 1.42-1.75,p <0.00001)和结直肠癌(OR = 1.67,95%CI = 1.24-2.26,p = 0.0008)。我们还发现了CHEK2 I157T变异与家族病例的相关性(OR = 1.85,95%CI = 1.51-2.26,p <0.00001)。但是,尚未建立与其他类型癌症的关联(OR = 1.09,95%CI = 0.75-1.57,p = 0.66)。这项荟萃分析表明,CHEK2 I157T变异体是重要的癌症基因,特别是在白种人的乳腺癌和结直肠癌中,这增加了癌症风险,生物信息学分析表明,这种变化主要归因于CHEK2 157T的疏水性降低。

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