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首页> 外文期刊>Asia-Pacific journal of clinical oncology >Association of APOBEC3 deletion with cancer risk: A meta‐analysis of 26?225 cases and 37?201 controls
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Association of APOBEC3 deletion with cancer risk: A meta‐analysis of 26?225 cases and 37?201 controls

机译:Apobec3缺失与癌症风险的关联:26〜225个案例和37次控件的Meta分析

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Abstract Previous studies have found inconsistent results regarding gene deletion in APOBEC3 (apolipoprotein B mRNA‐editing catalytic polypeptide‐like 3) and risk of cancer. We conducted a meta‐analysis of all eligible case–control studies to find out the associations between APOBEC3 deletion and cancer risk by pooling the odds ratios (ORs) and corresponding 95% confidence intervals (CIs). Overall, the findings from 20 studies (13 articles) involving of a total of 26?225 cases and 37?201 controls revealed that DD genotype was associated significantly with increased cancer risk compared to II genotype (OR?=?1.25, 95% CI?=?1.01–1.56, P ?=?0.04). Stratified analysis from 10 studies including 14?757 cases and 17?930 controls revealed that I/D variant significantly increased the risk of breast cancer in heterozygous codominant (OR?=?1.15, 95% CI?=?1.03–1.28, P ?=?0.02, ID vs II), dominant (OR?=?1.15, 95% CI?=?1.01–1.31, P ?=?0.03, ID?+?DD vs II), overdominant (OR?=?1.11, 95% CI?=?1.05–1.25, P ??0.0001, ID vs DD?+?II) and allele (OR?=?1.15, 95% CI?=?1.13–1.25, P ?=?0.03, D vs I) inheritance models. In conclusion, the data propose that APOBEC3 deletion is significantly associated with increased susceptibility to cancer in overall and breast cancer. Our findings require well‐designed replication in a larger independent genetic association study with larger sample sizes in diverse ethnicities.
机译:摘要以前的研究发现关于Apobec3(载脂蛋白B mRNA编辑催化多肽样3)中的基因缺失的不一致结果以及癌症的风险。我们对所有符合条件的账例控制研究进行了荟萃分析,以通过汇集多项目标比率(或者)和相应的95%置信区间(CIS)来了解APOBEC3缺失和癌症风险之间的关联。总体而言,来自20项研究(13篇文章)的发现,涉及共26例,325例,37?201对照表明,与II基因型(或?= 1.25,95%,95%,95%,95%,95%CI ?=?1.01-1.56,p?= 0.04)。来自10项研究的分层分析,包括14〜757例和17例,17°?930对照表明,I / D变体显着提高了杂合性Codominant(或?=α1.15,95%CI的乳腺癌的风险(或?1.1.15,95%,P?1.03-1.28,P? =?0.02,ID Vs II),优势(或?=?1.15,95%CI?=?1.01-1.31,P?=?0.03,ID?+?DD Vs II),Operdoinant(或?=?1.11, 95%ci?=?1.05-1.25,p?0.0001,Id Vs dd?+?II)和等位基因(或?=?1.15,95%ci?=?1.13-1.25,p?= 0.03, d vs i)继承模型。总之,数据提出了Apobec3缺失与总体和乳腺癌的癌症易感性增加显着相关。我们的研究结果需要在更大的独立遗传协会研究中进行精心设计的复制,并在各种各样的种族中具有较大的样本尺寸。

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