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Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls

机译:东亚女性乳腺癌风险的常见遗传决定因素:一项针对23637例乳腺癌病例和25579例对照的合作研究

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摘要

In a consortium including 23 637 breast cancer patients and 25 579 controls of East Asian ancestry, we investigated 70 single-nucleotide polymorphisms (SNPs) in 67 independent breast cancer susceptibility loci recently identified by genome-wide association studies (GWASs) conducted primarily in European-ancestry populations. SNPs in 31 loci showed an association with breast cancer risk at P < 0.05 in a direction consistent with that reported previously. Twenty-one of them remained statistically significant after adjusting for multiple comparisons with the Bonferroni-corrected significance level of <0.0015. Eight of the 70 SNPs showed a significantly different association with breast cancer risk by estrogen receptor (ER) status at P < 0.05. With the exception of rs2046210 at 6q25.1, the seven other SNPs showed a stronger association with ER-positive than ER-negative cancer. This study replicated all five genetic risk variants initially identified in Asians and provided evidence for associations of breast cancer risk in the East Asian population with nearly half of the genetic risk variants initially reported in GWASs conducted in European descendants. Taken together, these common genetic risk variants explain ∼10% of excess familial risk of breast cancer in Asian populations.
机译:在一个包括23637名乳腺癌患者和25579名东亚血统对照的财团中,我们调查了67个独立的乳腺癌易感性基因座中的70个单核苷酸多态性(SNP),这些基因组最近在欧洲主要通过全基因组关联研究(GWAS)确定族人口。在31个基因座中的SNPs与乳腺癌风险呈正相关(P <0.05),其方向与先前报道的一致。在用Bonferroni校正的显着性水平<0.0015进行多次比较调整后,其中有21个在统计学上仍然显着。在70个SNP中,有八个显示出雌激素受体(ER)状态与乳腺癌风险显着不同,P <0.05。除了在6q25.1的rs2046210外,其他七个SNP与ER阳性的癌症比与ER阴性的癌症之间的关联更强。这项研究复制了最初在亚洲人中发现的所有五个遗传风险变体,并为东亚人群中乳腺癌风险与欧洲后代在GWAS中最初报道的遗传风险变体中近一半的关联提供了证据。综合起来,这些常见的遗传风险变量可解释约10%的亚洲人群患乳腺癌的家族性额外风险。

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