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GWAS Study

Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers.

Lesseur C, Ferreiro-Iglesias A, McKay JD et al.

33667223 PubMed ID
GWAS Study Type
75848 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LC
Lesseur C
FA
Ferreiro-Iglesias A
MJ
McKay JD
BY
Bossé Y
JM
Johansson M
GV
Gaborieau V
LM
Landi MT
CD
Christiani DC
CN
Caporaso NC
BS
Bojesen SE
AC
Amos CI
SS
Shete S
LG
Liu G
RG
Rennert G
AD
Albanes D
AM
Aldrich MC
TA
Tardon A
CC
Chen C
TL
Triantafillos L
FJ
Field JK
TM
Teare MD
KL
Kiemeney LA
DB
Diergaarde B
FR
Ferris RL
ZS
Zienolddiny S
LS
Lam S
OA
Olshan AF
WM
Weissler MC
LM
Lacko M
RA
Risch A
BH
Bickeböller H
NA
Ness AR
TS
Thomas S
LM
Le Marchand L
SM
Schabath MB
WV
Wünsch-Filho V
TE
Tajara EH
AA
Andrew AS
CG
Clifford GM
LP
Lazarus P
GK
Grankvist K
JM
Johansson M
AS
Arnold S
MO
Melander O
BH
Brunnström H
BS
Boccia S
CG
Cadoni G
TW
Timens W
OM
Obeidat M
XX
Xiao X
HR
Houlston RS
HR
Hung RJ
BP
Brennan P
Chapter II

Abstract

Summary of the research findings

Squamous cell carcinomas (SqCC) of the aerodigestive tract have similar etiological risk factors. Although genetic risk variants for individual cancers have been identified, an agnostic, genome-wide search for shared genetic susceptibility has not been performed. To identify novel and pleotropic SqCC risk variants, we performed a meta-analysis of GWAS data on lung SqCC (LuSqCC), oro/pharyngeal SqCC (OSqCC), laryngeal SqCC (LaSqCC) and esophageal SqCC (ESqCC) cancers, totaling 13,887 cases and 61,961 controls of European ancestry. We identified one novel genome-wide significant (Pmeta<5x10-8) aerodigestive SqCC susceptibility loci in the 2q33.1 region (rs56321285, TMEM273). Additionally, three previously unknown loci reached suggestive significance (Pmeta<5x10-7): 1q32.1 (rs12133735, near MDM4), 5q31.2 (rs13181561, TMEM173) and 19p13.11 (rs61494113, ABHD8). Multiple previously identified loci for aerodigestive SqCC also showed evidence of pleiotropy in at least another SqCC site, these include: 4q23 (ADH1B), 6p21.33 (STK19), 6p21.32 (HLA-DQB1), 9p21.33 (CDKN2B-AS1) and 13q13.1(BRCA2). Gene-based association and gene set enrichment identified a set of 48 SqCC-related genes rel to DNA damage and epigenetic regulation pathways. Our study highlights the importance of cross-cancer analyses to identify pleiotropic risk loci of histology-related cancers arising at distinct anatomical sites.

7,426 European ancestry lung squamous cell carcinoma cases, 5,452 European ancestry oral and oropharynx squamous cell carcinoma cases, 693 European ancestry laryngeal squamous cell carcinoma cases, 316 European ancestry esophageal squamous cell carcinoma cases, 61,961 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

75848
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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