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Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

  • SpiroMeta Consortium
  • International Agency for Research on Cancer
  • University of Toronto
  • Dartmouth College
  • Massachusetts General Hospital
  • National Institutes of Health
  • University of Cambridge
  • University of Copenhagen
  • University of Texas MD Anderson Cancer Center
  • University of Hawai'i at Mānoa
  • University of Göttingen
  • Vanderbilt University
  • Case Western Reserve University
  • University of Oviedo
  • Clalit Health Services
  • University of Sheffield
  • University of Liverpool
  • Radboud University Nijmegen
  • National Institute of Occupational Health
  • Provincial Health Services Authority
  • Moffitt Cancer Center
  • Nanjing Medical University
  • Seoul National University
  • University of Pittsburgh
  • IRCCS Fondazione Ca'Granda – Ospedale Maggiore Policlinico - Milano
  • University of Milan
  • University Health Network
  • University of Southern California

Research output: Contribution to journalArticlepeer-review

585 Scopus citations

Abstract

Although several lung cancer susceptibility loci have been identified, much of the heritability for lung cancer remains unexplained. Here 14,803 cases and 12,262 controls of European descent were genotyped on the OncoArray and combined with existing data for an aggregated genome-wide association study (GWAS) analysis of lung cancer in 29,266 cases and 56,450 controls. We identified 18 susceptibility loci achieving genome-wide significance, including 10 new loci. The new loci highlight the striking heterogeneity in genetic susceptibility across the histological subtypes of lung cancer, with four loci associated with lung cancer overall and six loci associated with lung adenocarcinoma. Gene expression quantitative trait locus (eQTL) analysis in 1,425 normal lung tissue samples highlights RNASET2, SECISBP2L and NRG1 as candidate genes. Other loci include genes such as a cholinergic nicotinic receptor, CHRNA2, and the telomere-related genes OFBC1 and RTEL1. Further exploration of the target genes will continue to provide new insights into the etiology of lung cancer.

Original languageEnglish
Pages (from-to)1126-1132
Number of pages7
JournalNature Genetics
Volume49
Issue number7
DOIs
StatePublished - Jul 1 2017

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