Shared heritability and functional enrichment across six solid cancers
dc.contributor.author
dc.date.accessioned
2020-06-26T09:34:20Z
dc.date.available
2020-06-26T09:34:20Z
dc.date.issued
2019-01-29
dc.identifier.issn
2041-1723
dc.identifier.uri
dc.description.abstract
Quantifying 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
dc.format.mimetype
application/pdf
dc.language.iso
eng
dc.publisher
Nature Research
dc.relation.isformatof
Reproducció digital del document publicat a: https://doi.org/10.1038/s41467-018-08054-4
dc.relation.ispartof
Nature Communications, 2019, vol. 10, art. núm. 431
dc.relation.ispartofseries
Articles publicats (IdIBGi)
dc.rights
Attribution 4.0 International
dc.rights.uri
dc.subject
dc.title
Shared heritability and functional enrichment across six solid cancers
dc.type
info:eu-repo/semantics/article
dc.rights.accessRights
info:eu-repo/semantics/openAccess
dc.type.version
info:eu-repo/semantics/publishedVersion
dc.identifier.doi
dc.type.peerreviewed
peer-reviewed
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