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GWAS Study

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer.

Byun J, Han Y, Li Y et al.

35915169 PubMed ID
GWAS Study Type
1008284 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BJ
Byun J
HY
Han Y
LY
Li Y
XJ
Xia J
LE
Long E
CJ
Choi J
XX
Xiao X
ZM
Zhu M
ZW
Zhou W
SR
Sun R
BY
Bossé Y
SZ
Song Z
SA
Schwartz A
LC
Lusk C
RT
Rafnar T
SK
Stefansson K
ZT
Zhang T
ZW
Zhao W
PR
Pettit RW
LY
Liu Y
LX
Li X
ZH
Zhou H
WK
Walsh KM
GI
Gorlov I
GO
Gorlova O
ZD
Zhu D
RS
Rosenberg SM
PS
Pinney S
BJ
Bailey-Wilson JE
MD
Mandal D
DA
de Andrade M
GC
Gaba C
WJ
Willey JC
YM
You M
AM
Anderson M
WJ
Wiencke JK
AD
Albanes D
LS
Lam S
TA
Tardon A
CC
Chen C
GG
Goodman G
BS
Bojeson S
BH
Brenner H
LM
Landi MT
CS
Chanock SJ
JM
Johansson M
MT
Muley T
RA
Risch A
WH
Wichmann HE
BH
Bickeböller H
CD
Christiani DC
RG
Rennert G
AS
Arnold S
FJ
Field JK
SS
Shete S
LM
Le Marchand L
MO
Melander O
BH
Brunnstrom H
LG
Liu G
AA
Andrew AS
KL
Kiemeney LA
SH
Shen H
ZS
Zienolddiny S
GK
Grankvist K
JM
Johansson M
CN
Caporaso N
CA
Cox A
HY
Hong YC
YJ
Yuan JM
LP
Lazarus P
SM
Schabath MB
AM
Aldrich MC
PA
Patel A
LQ
Lan Q
RN
Rothman N
TF
Taylor F
KL
Kachuri L
WJ
Witte JS
SL
Sakoda LC
SM
Spitz M
BP
Brennan P
LX
Lin X
MJ
McKay J
HR
Hung RJ
AC
Amos CI
Chapter II

Abstract

Summary of the research findings

To identify new susceptibility loci to lung cancer among diverse populations, we performed cross-ancestry genome-wide association studies in European, East Asian and African populations and discovered five loci that have not been previously reported. We replicated 26 signals and identified 10 new lead associations from previously reported loci. Rare-variant associations tended to be specific to populations, but even common-variant associations influencing smoking behavior, such as those with CHRNA5 and CYP2A6, showed population specificity. Fine-mapping and expression quantitative trait locus colocalization nominated several candidate variants and susceptibility genes such as IRF4 and FUBP1. DNA damage assays of prioritized genes in lung fibroblasts indicated that a subset of these genes, including the pleiotropic gene IRF4, potentially exert effects by promoting endogenous DNA damage.

26,683 European ancestry cases, 25,278 European ancestry controls, 7,062 East Asian ancestry cases, 5,372 East Asian ancestry controls, 1,987 African American cases, 3,774 African American controls

Chapter III

Study Statistics

Key metrics and study information

1008284
Total Participants
GWAS
Study Type
Yes
Replicated
11,680 European ancestry cases, 898,929 European ancestry controls, 13,316 East Asian ancestry cases, 13,324 East Asian ancestry controls, 319 African American cases, 560 African American controls
Replication Participants
European, East Asian, African American or Afro-Caribbean
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.