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Shared heritability and functional enrichment across six solid cancers
dc.contributor.author | Jiang, X. | |
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dc.contributor.author | Schumacher, F. R. | |
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dc.date.accessioned | 2021-10-13T10:48:06Z | |
dc.date.available | 2021-10-13T10:48:06Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 2041-1723 | |
dc.identifier.other | https://www.ncbi.nlm.nih.gov/pubmed/30683880 | |
dc.identifier.other | http://diposit.ub.edu/dspace/bitstream/2445/171263/1/698689.pdf | |
dc.identifier.uri | http://hdl.handle.net/20.500.11940/15483 | |
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 x 10(-8)), breast and ovarian cancer (rg = 0.24, p = 7 x 10(-5)), breast and lung cancer (rg = 0.18, p =1.5 x 10(-6)) and breast and colorectal cancer (rg = 0.15, p = 1.1 x 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.rights | Atribución 4.0 Internacional | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.title | Shared heritability and functional enrichment across six solid cancers | |
dc.type | Artigo | es |
dc.authorsophos | Vega Gliemmo, Ana | |
dc.authorsophos | Gago Dominguez, Manuela | |
dc.identifier.doi | 10.1038/s41467-018-08054-4 | |
dc.identifier.pmid | 30683880 | |
dc.identifier.sophos | 30814 | |
dc.issue.number | 1 | |
dc.journal.title | Nature Communications | |
dc.organization | Servizo Galego de Saúde::Dirección Xeral de Asistencia Sanitaria::Fundación Pública Galega de Medicina Xenómica | |
dc.organization | Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS) | |
dc.organization | Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Xenética | |
dc.page.initial | 431 | es |
dc.rights.accessRights | openAccess | |
dc.subject.keyword | CHUS | |
dc.subject.keyword | IDIS | |
dc.typefides | Artículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis) | |
dc.typesophos | Artículo Original | |
dc.volume.number | 10 |