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Paternal lineage early onset hereditary ovarian cancers: A Familial Ovarian Cancer Registry study

机译:父系世袭早期遗传性卵巢癌:家族性卵巢癌注册研究

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摘要

Given prior evidence that an affected woman conveys a higher risk of ovarian cancer to her sister than to her mother, we hypothesized that there exists an X-linked variant evidenced by transmission to a woman from her paternal grandmother via her father. We ascertained 3,499 grandmother/granddaughter pairs from the Familial Ovarian Cancer Registry at the Roswell Park Cancer Institute observing 892 informative pairs with 157 affected granddaughters. We performed germline X-chromosome exome sequencing on 186 women with ovarian cancer from the registry. The rate of cancers was 28.4% in paternal grandmother/granddaughter pairs and 13.9% in maternal pairs consistent with an X-linked dominant model (Chi-square test X2 = 0.02, p = 0.89) and inconsistent with an autosomal dominant model (X2 = 20.4, p<0.001). Paternal grandmother cases had an earlier age-of-onset versus maternal cases (hazard ratio HR = 1.59, 95%CI: 1.12–2.25) independent of BRCA1/2 status. Reinforcing the X-linked hypothesis, we observed an association between prostate cancer in men and ovarian cancer in his mother and daughters (odds ratio, OR = 2.34, p = 0.034). Unaffected mothers with affected daughters produced significantly more daughters than sons (ratio = 1.96, p<0.005). We performed exome sequencing in reported BRCA negative cases from the registry. Considering age-of-onset, one missense variant (rs176026 in MAGEC3) reached chromosome-wide significance (Hazard ratio HR = 2.85, 95%CI: 1.75–4.65) advancing the age of onset by 6.7 years. In addition to the well-known contribution of BRCA, we demonstrate that a genetic locus on the X-chromosome contributes to ovarian cancer risk. An X-linked pattern of inheritance has implications for genetic risk stratification. Women with an affected paternal grandmother and sisters of affected women are at increased risk for ovarian cancer. Further work is required to validate this variant and to characterize carrier families.
机译:鉴于先前的证据表明,受感染的女性对其姐姐比母亲具有更高的卵巢癌风险,我们假设存在一个X连锁变体,可以通过父亲从其祖母传染给一名女性来证明。我们从罗斯韦尔公园癌症研究所的家族性卵巢癌登记处确定了3499对祖母/孙女,观察了892对信息对和157名受影响的孙女。我们对来自注册表的186名卵巢癌女性进行了生殖系X染色体外显子组测序。与X连锁显性模型一致(卡方检验X2 = 0.02,p = 0.89),与常染色体显性模型不一致(X2 = X),在父/母/孙对中,癌症的发生率为28.4%,在母对中,癌症的发生率为13.9%。 20.4,p <0.001)。与BRCA1 / 2状态无关,祖母病例的发病年龄要比母体病例的发病年龄早(母亲的危险比HR = 1.59,95%CI:1.12–2.25)。加强了X连锁假设,我们观察到男性前列腺癌与他的母女卵巢癌之间的关联(比值比,OR = 2.34,p = 0.034)。未受影响的母亲和受影响的女儿所生的女儿比儿子多得多(比率= 1.96,p <0.005)。我们在注册表中报告的BRCA阴性病例中进行了外显子组测序。考虑到发病年龄,一种错义变体(MAGEC3中的rs176026)达到了全染色体显着性(危险比HR = 2.85,95%CI:1.75–4.65),将发病年龄提高了6.7岁。除了BRCA的著名贡献外,我们还证明了X染色体上的基因座也有助于卵巢癌。 X连锁遗传模式对遗传风险分层有影响。患病的祖母和受其感染的姐妹的妇女患卵巢癌的风险增加。需要进一步的工作来验证该变体并表征运营商系列。

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