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000142873 0247_ $$2doi$$a10.1038/s41467-018-08054-4
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000142873 0247_ $$2pmc$$apmc:PMC6347624
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000142873 037__ $$aDKFZ-2019-00503
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000142873 082__ $$a500
000142873 1001_ $$aJiang, Xia$$b0
000142873 245__ $$aShared heritability and functional enrichment across six solid cancers.
000142873 260__ $$a[London]$$bNature Publishing Group UK$$c2019
000142873 3367_ $$2DRIVER$$aarticle
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000142873 520__ $$aQuantifying the genetic correlation between cancers can provide important insights into the mechanisms driving cancer etiology. Using genome-wide association study summary statistics across six cancer types based on a total of 296,215 cases and 301,319 controls of European ancestry, here we estimate the pair-wise genetic correlations between breast, colorectal, head/neck, lung, ovary and prostate cancer, and between cancers and 38 other diseases. We observed statistically significant genetic correlations between lung and head/neck cancer (rg = 0.57, p = 4.6 × 10-8), breast and ovarian cancer (rg = 0.24, p = 7 × 10-5), breast and lung cancer (rg = 0.18, p =1.5 × 10-6) and breast and colorectal cancer (rg = 0.15, p = 1.1 × 10-4). We also found that multiple cancers are genetically correlated with non-cancer traits including smoking, psychiatric diseases and metabolic characteristics. Functional enrichment analysis revealed a significant excess contribution of conserved and regulatory regions to cancer heritability. Our comprehensive analysis of cross-cancer heritability suggests that solid tumors arising across tissues share in part a common germline genetic basis.
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000142873 7001_ $$aTyrer, Jonathan P$$b4
000142873 7001_ $$aHan, Younghun$$b5
000142873 7001_ $$00000-0001-7065-1237$$aMichailidou, Kyriaki$$b6
000142873 7001_ $$aLesseur, Corina$$b7
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