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Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types

  • Joshua N. Sampson
  • , William A. Wheeler
  • , Meredith Yeager
  • , Orestis Panagiotou
  • , Zhaoming Wang
  • , Sonja I. Berndt
  • , Qing Lan
  • , Christian C. Abnet
  • , Laufey T. Amundadottir
  • , Jonine D. Figueroa
  • , Maria Teresa Landi
  • , Lisa Mirabello
  • , Sharon A. Savage
  • , Philip R. Taylor
  • , Immaculata De Vivo
  • , Katherine A. McGlynn
  • , Mark P. Purdue
  • , Preetha Rajaraman
  • , Hans Olov Adami
  • , Anders Ahlbom
  • Demetrius Albanes, Maria Fernanda Amary, She Juan An, Ulrika Andersson, Gerald Andriole, Irene L. Andrulis, Emanuele Angelucci, Stephen M. Ansell, Cecilia Arici, Bruce K. Armstrong, Alan A. Arslan, Melissa A. Austin, Dalsu Baris, Donald A. Barkauskas, Bryan A. Bassig, Nikolaus Becker, Yolanda Benavente, Simone Benhamou, Christine Berg, David Van Den Berg, Leslie Bernstein, Kimberly A. Bertrand, Brenda M. Birmann, Amanda Black, Heiner Boeing, Paolo Boffetta, Marie Christine Boutron-Ruault, Paige M. Bracci, Louise Brinton, Angela R. Brooks-Wilson, H. Bas Bueno-De-Mesquita, Laurie Burdett, Julie Buring, Mary Ann Butler, Qiuyin Cai, Geraldine Cancel-Tassin, Federico Canzian, Alfredo Carrato, Tania Carreon, Angela Carta, John K.C. Chan, Ellen T. Chang, Gee Chen Chang, I. 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Research output: Contribution to journalArticlepeer-review

142 Scopus citations

Abstract

Background: Studies of related individuals have consistently demonstrated notable familial aggregation of cancer. We aim to estimate the heritability and genetic correlation attributable to the additive effects of common single-nucleotide polymorphisms (SNPs) for cancer at 13 anatomical sites. Methods: Between 2007 and 2014, the US National Cancer Institute has generated data from genome-wide association studies (GWAS) for 49 492 cancer case patients and 34 131 control patients. We apply novel mixed model methodology (GCTA) to this GWAS data to estimate the heritability of individual cancers, as well as the proportion of heritability attributable to cigarette smoking in smoking-related cancers, and the genetic correlation between pairs of cancers. Results: GWAS heritability was statistically significant at nearly all sites, with the estimates of array-based heritability, hl 2, on the liability threshold (LT) scale ranging from 0.05 to 0.38. Estimating the combined heritability of multiple smoking characteristics, we calculate that at least 24% (95% confidence interval [CI] = 14% to 37%) and 7% (95% CI = 4% to 11%) of the heritability for lung and bladder cancer, respectively, can be attributed to genetic determinants of smoking. Most pairs of cancers studied did not show evidence of strong genetic correlation. We found only four pairs of cancers with marginally statistically significant correlations, specifically kidney and testes (ρ = 0.73, SE = 0.28), diffuse large B-cell lymphoma (DLBCL) and pediatric osteosarcoma (ρ = 0.53, SE = 0.21), DLBCL and chronic lymphocytic leukemia (CLL) (ρ = 0.51, SE =0.18), and bladder and lung (ρ = 0.35, SE = 0.14). Correlation analysis also indicates that the genetic architecture of lung cancer differs between a smoking population of European ancestry and a nonsmoking Asian population, allowing for the possibility that the genetic etiology for the same disease can vary by population and environmental exposures. Conclusion: Our results provide important insights into the genetic architecture of cancers and suggest new avenues for investigation.

Original languageEnglish
JournalJournal of the National Cancer Institute
Volume107
Issue number12
DOIs
StatePublished - Dec 2015

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