Skip to main content

Lund University Publications

LUND UNIVERSITY LIBRARIES

Shared heritability and functional enrichment across six solid cancers

Jiang, Xia ; Brunnström, Hans LU orcid ; Ellberg, Carolina LU orcid ; Olsson, Håkan LU orcid and Lindström, Sara (2019) In Nature Communications 10(1). p.1-23
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... (More)
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. © 2019, The Author(s). (Less)
Please use this url to cite or link to this publication:
author
; ; ; and
author collaboration
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Nature Communications
volume
10
issue
1
article number
431
pages
1 - 23
publisher
Nature Publishing Group
external identifiers
  • scopus:85060528251
  • pmid:30683880
ISSN
2041-1723
DOI
10.1038/s41467-018-08054-4
language
English
LU publication?
yes
additional info
Export Date: 5 February 2019
id
5f5c9536-f446-4642-823d-bafa1823de82
date added to LUP
2019-02-05 12:04:23
date last changed
2024-01-30 09:32:08
@article{5f5c9536-f446-4642-823d-bafa1823de82,
  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. © 2019, The Author(s).}},
  author       = {{Jiang, Xia and Brunnström, Hans and Ellberg, Carolina and Olsson, Håkan and Lindström, Sara}},
  issn         = {{2041-1723}},
  language     = {{eng}},
  number       = {{1}},
  pages        = {{1--23}},
  publisher    = {{Nature Publishing Group}},
  series       = {{Nature Communications}},
  title        = {{Shared heritability and functional enrichment across six solid cancers}},
  url          = {{http://dx.doi.org/10.1038/s41467-018-08054-4}},
  doi          = {{10.1038/s41467-018-08054-4}},
  volume       = {{10}},
  year         = {{2019}},
}