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GWAS Study

A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.

Landi MT, Chatterjee N, Yu K et al.

19836008 PubMed ID
GWAS Study Type
32966 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Landi MT
CN
Chatterjee N
YK
Yu K
GL
Goldin LR
GA
Goldstein AM
RM
Rotunno M
ML
Mirabello L
JK
Jacobs K
WW
Wheeler W
YM
Yeager M
BA
Bergen AW
LQ
Li Q
CD
Consonni D
PA
Pesatori AC
WS
Wacholder S
TM
Thun M
DR
Diver R
OM
Oken M
VJ
Virtamo J
AD
Albanes D
WZ
Wang Z
BL
Burdette L
DK
Doheny KF
PE
Pugh EW
LC
Laurie C
BP
Brennan P
HR
Hung R
GV
Gaborieau V
MJ
McKay JD
LM
Lathrop M
MJ
McLaughlin J
WY
Wang Y
TM
Tsao MS
SM
Spitz MR
WY
Wang Y
KH
Krokan H
VL
Vatten L
SF
Skorpen F
AE
Arnesen E
BS
Benhamou S
BC
Bouchard C
MA
Metspalu A
MA
Metsapalu A
VT
Vooder T
NM
Nelis M
VK
Välk K
FJ
Field JK
CC
Chen C
GG
Goodman G
SP
Sulem P
TG
Thorleifsson G
RT
Rafnar T
ET
Eisen T
SW
Sauter W
RA
Rosenberger A
BH
Bickeböller H
RA
Risch A
CJ
Chang-Claude J
WH
Wichmann HE
SK
Stefansson K
HR
Houlston R
AC
Amos CI
FJ
Fraumeni JF
SS
Savage SA
BP
Bertazzi PA
TM
Tucker MA
CS
Chanock S
CN
Caporaso NE
Chapter II

Abstract

Summary of the research findings

Three genetic loci for lung cancer risk have been identified by genome-wide association studies (GWAS), but inherited susceptibility to specific histologic types of lung cancer is not well established. We conducted a GWAS of lung cancer and its major histologic types, genotyping 515,922 single-nucleotide polymorphisms (SNPs) in 5739 lung cancer cases and 5848 controls from one population-based case-control study and three cohort studies. Results were combined with summary data from ten additional studies, for a total of 13,300 cases and 19,666 controls of European descent. Four studies also provided histology data for replication, resulting in 3333 adenocarcinomas (AD), 2589 squamous cell carcinomas (SQ), and 1418 small cell carcinomas (SC). In analyses by histology, rs2736100 (TERT), on chromosome 5p15.33, was associated with risk of adenocarcinoma (odds ratio [OR]=1.23, 95% confidence interval [CI]=1.13-1.33, p=3.02x10(-7)), but not with other histologic types (OR=1.01, p=0.84 and OR=1.00, p=0.93 for SQ and SC, respectively). This finding was confirmed in each replication study and overall meta-analysis (OR=1.24, 95% CI=1.17-1.31, p=3.74x10(-14) for AD; OR=0.99, p=0.69 and OR=0.97, p=0.48 for SQ and SC, respectively). Other previously reported association signals on 15q25 and 6p21 were also refined, but no additional loci reached genome-wide significance. In conclusion, a lung cancer GWAS identified a distinct hereditary contribution to adenocarcinoma.

5,739 European ancestry cases, 5,848 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

32966
Total Participants
GWAS
Study Type
Yes
Replicated
7,561 European ancestry cases, 13,818 European ancestry controls
Replication Participants
European
Ancestry
U.S., Poland, Czech Republic, Iceland, Russian Federation, Romania, Canada, Germany, U.K., Estonia, Hungary, Slovakia, France, Norway, Finland, Italy
Recruitment Country
Chapter IV

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