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Genome-wide association study for lung cancer in 6531 African Americans reveals new susceptibility loci

  • INTEGRAL-ILCCO Consortium
  • Baylor College of Medicine
  • University of New Mexico
  • National Institutes of Health
  • University of Texas Health Science Center at Houston
  • Wayne State University
  • Chinese Academy of Medical Sciences
  • Stanford University
  • Duke University
  • University of California at San Francisco
  • University of British Columbia
  • University of Oviedo
  • Fred Hutchinson Cancer Research Center
  • University of Copenhagen
  • German Cancer Research Center
  • International Agency for Research on Cancer
  • Member of the German Center for Lung Research (DZL)
  • University of Salzburg
  • Helmholtz-Munich Institute of Epidemiology
  • University of Göttingen
  • Harvard University
  • Clalit Health Services
  • University of Kentucky
  • University of Liverpool
  • University of Texas MD Anderson Cancer Center
  • University of Hawai'i at Mānoa
  • University Health Network
  • Dartmouth College
  • National Institute of Occupational Health
  • Umeå University
  • Sheffield Teaching Hospitals NHS Foundation Trust
  • Moffitt Cancer Center
  • Vanderbilt University
  • American Cancer Society

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

Despite lung cancer affecting all races and ethnicities, disparities are observed in incidence and mortality rates among different ethnic groups in the United States. Non-Hispanic African Americans had a high incidence rate of lung cancer at 55.8 per 100 000 people, as well as the highest death rate at 37.2 per 100 000 people from 2016 to 2020. While previous genome-wide association studies (GWAS) have identified over 45 susceptibility risk loci that inf luence lung cancer development, few GWAS have investigated the etiology of lung cancer in African Americans. To address this gap in knowledge, we conducted GWAS of lung cancer focused on studying African Americans, comprising 2267 lung cancer cases and 4264 controls. We identified three loci associated with lung cancer, one with lung adenocarcinoma, and four with lung squamous cell carcinoma in this population at the genomic-wide significance level. Among them, three novel loci were identified near VWF at 12p13.31 for overall lung cancer and GACAT3 at 2p24.3 and LMAN1L at 15q24.1 for lung squamous cell carcinoma. In addition, we confirmed previously reported risk loci with known or new lead variants near CHRNA5 at 15q25.1 and CYP2A6 at 19q13.2 associated with lung cancer and TRIP13 at 5p15.33 and ERC1 at 12p13.33 associated with lung squamous cell carcinoma. Further multi-step functional analyses shed light on biological mechanisms underlying these associations of lung cancer in this population. Our study highlights the importance of ancestry-specific studies for the potential alleviation of lung cancer burden in African Americans.

Original languageEnglish
Pages (from-to)1227-1237
Number of pages11
JournalHuman Molecular Genetics
Volume34
Issue number14
DOIs
StatePublished - Jul 15 2025

Keywords

  • African American
  • Genome-wide association study
  • Lung cancer
  • Polygenic risk score
  • Post-GWAS

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