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Rare deleterious germline variants and risk of lung cancer
Y. Liu, J. Xia, J. McKay, S. Tsavachidis, X. Xiao, MR. Spitz, C. Cheng, J. Byun, W. Hong, Y. Li, D. Zhu, Z. Song, SM. Rosenberg, ME. Scheurer, F. Kheradmand, CW. Pikielny, CM. Lusk, AG. Schwartz, II. Wistuba, MH. Cho, EK. Silverman, J....
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
U01 CA209414
NCI NIH HHS - United States
NLK
Directory of Open Access Journals
od 2017
PubMed Central
od 2017
Europe PubMed Central
od 2017
ProQuest Central
od 2017-01-01
Nursing & Allied Health Database (ProQuest)
od 2017-01-01
Health & Medicine (ProQuest)
od 2017-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2017
Springer Nature OA/Free Journals
od 2017-12-01
Springer Nature - nature.com Journals - Fully Open Access
od 2017-12-01
- Publikační typ
- časopisecké články MeSH
Recent studies suggest that rare variants exhibit stronger effect sizes and might play a crucial role in the etiology of lung cancers (LC). Whole exome plus targeted sequencing of germline DNA was performed on 1045 LC cases and 885 controls in the discovery set. To unveil the inherited causal variants, we focused on rare and predicted deleterious variants and small indels enriched in cases or controls. Promising candidates were further validated in a series of 26,803 LCs and 555,107 controls. During discovery, we identified 25 rare deleterious variants associated with LC susceptibility, including 13 reported in ClinVar. Of the five validated candidates, we discovered two pathogenic variants in known LC susceptibility loci, ATM p.V2716A (Odds Ratio [OR] 19.55, 95%CI 5.04-75.6) and MPZL2 p.I24M frameshift deletion (OR 3.88, 95%CI 1.71-8.8); and three in novel LC susceptibility genes, POMC c.*28delT at 3' UTR (OR 4.33, 95%CI 2.03-9.24), STAU2 p.N364M frameshift deletion (OR 4.48, 95%CI 1.73-11.55), and MLNR p.Q334V frameshift deletion (OR 2.69, 95%CI 1.33-5.43). The potential cancer-promoting role of selected candidate genes and variants was further supported by endogenous DNA damage assays. Our analyses led to the identification of new rare deleterious variants with LC susceptibility. However, in-depth mechanistic studies are still needed to evaluate the pathogenic effects of these specific alleles.
Department of Biomedical Data Science Geisel School of Medicine Dartmouth College Lebanon NH USA
Department of Molecular and Human Genetics Baylor College of Medicine Houston TX USA
Department of Pediatrics Baylor College of Medicine Houston TX USA
Faculty of Health Sciences Palacky University Olomouc Czech Republic
Harvard University T H Chan School of Public Health Boston MA USA
Institute for Clinical and Translational Research Baylor College of Medicine Houston TX USA
International Agency for Research on Cancer Lyon France
Karmanos Cancer Institute Wayne State University Detroit MI USA
Louisiana State University Health Sciences Center New Orleans LA USA
Lunenfeld Tanenbaum Research Institute Sinai Health System Toronto ON Canada
M Sklodowska Curie National Research Institute of Oncology Warsaw Poland
Mayo Clinic College of Medicine Rochester MN USA
Mayo Clinic College of Medicine Scottsdale AZ USA
Medical College of Wisconsin Milwaukee WI USA
Michael E DeBakey Veterans Affairs Medical Center Houston TX USA
National Human Genome Research Institute Bethesda MD USA
National Institute of Public Health Bucharest Romania
Nofer Institute of Occupational Medicine Department of Environmental Epidemiology Lodz Poland
Princess Margaret Cancer Center Toronto ON Canada
Russian N N Blokhin Cancer Research Centre Moscow Russian Federation
The University of Toledo College of Medicine Toledo OH USA
University of Cincinnati College of Medicine Cincinnati OH USA
Citace poskytuje Crossref.org
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- $a Recent studies suggest that rare variants exhibit stronger effect sizes and might play a crucial role in the etiology of lung cancers (LC). Whole exome plus targeted sequencing of germline DNA was performed on 1045 LC cases and 885 controls in the discovery set. To unveil the inherited causal variants, we focused on rare and predicted deleterious variants and small indels enriched in cases or controls. Promising candidates were further validated in a series of 26,803 LCs and 555,107 controls. During discovery, we identified 25 rare deleterious variants associated with LC susceptibility, including 13 reported in ClinVar. Of the five validated candidates, we discovered two pathogenic variants in known LC susceptibility loci, ATM p.V2716A (Odds Ratio [OR] 19.55, 95%CI 5.04-75.6) and MPZL2 p.I24M frameshift deletion (OR 3.88, 95%CI 1.71-8.8); and three in novel LC susceptibility genes, POMC c.*28delT at 3' UTR (OR 4.33, 95%CI 2.03-9.24), STAU2 p.N364M frameshift deletion (OR 4.48, 95%CI 1.73-11.55), and MLNR p.Q334V frameshift deletion (OR 2.69, 95%CI 1.33-5.43). The potential cancer-promoting role of selected candidate genes and variants was further supported by endogenous DNA damage assays. Our analyses led to the identification of new rare deleterious variants with LC susceptibility. However, in-depth mechanistic studies are still needed to evaluate the pathogenic effects of these specific alleles.
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