Susceptibility loci for lung cancer are associated with mRNA levels of nearby genes in the lung

Justin Dang Uy Nguyen, Maxime Lamontagne, Christian Couture, Massimo Conti, Peter D. Pare, Don D. Sin, James C. Hogg, David Nickle, Dirkje S. Postma, Wim Timens, Michel Laviolette, Yohan Bosse*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

17 Citations (Scopus)

Abstract

Recent studies identified three genetic loci reproducibly associated with lung cancer in populations of European ancestry, namely 15q25, 5p15 and 6p21. The goals of this study are first to confirm whether these loci are associated with lung cancer in a French Canadian population and second to identify disease-associated single nucleotide polymorphisms (SNPs) influencing messenger RNA (mRNA) expression levels of genes in the lung, that is expression quantitative trait loci (eQTLs). SNPs were genotyped in 420 patients undergoing lung cancer surgery and compared with 3151 controls of European ancestry. Genome-wide gene expression levels in non-tumor lung tissues of the same 420 patients were also measured to identify eQTLs. Significant eQTLs were then followed-up in two replication sets (n = 339 and 363). SNPs found in the three susceptibility loci were associated with lung cancer in the French Canadian population. Strong eQTLs were found on chromosome 15q25 with the expression levels of CHRNA5 (P = 2.23 x 10(-22) with rs12907966). The CHRNA5-rs12907966 eQTL was convincingly validated in the two replication sets (P = 3.46 x 10(-16) and 2.01 x 10(-15)). On 6p21, a trend was observed for rs3131379 to be associated with the expression of APOM (P = 3.58 x 10(-4)) and validated in the replication sets (P = 1.11 x 10(-8) and 6.84 x 10(-4)). On 5p15, no significant eQTLs were found. This study confirmed that chromosomes 15q25, 5p15 and 6p21 harbored susceptibility loci for lung cancer in French Canadians. Most importantly, this study suggests that the risk alleles at 15q25 and 6p21 may mediate their effect by regulating the mRNA expression levels of CHRNA5 and APOM in the lung.

Original languageEnglish
Pages (from-to)2653-2659
Number of pages7
JournalCARCINOGENESIS
Volume35
Issue number12
DOIs
Publication statusPublished - Dec-2014

Keywords

  • GENOME-WIDE ASSOCIATION
  • NICOTINE DEPENDENCE
  • IDENTIFY MULTIPLE
  • HEAVY SMOKING
  • NEVER-SMOKERS
  • RISK
  • VARIANTS
  • POPULATION
  • ADENOCARCINOMA
  • 5P15.33

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