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GWAS Study

Smoking modifies pancreatic cancer risk loci on 2q21.3.

Mocci E, Kundu P, Wheeler W et al.

33574088 PubMed ID
GWAS Study Type
19711 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ME
Mocci E
KP
Kundu P
WW
Wheeler W
AA
Arslan AA
BL
Beane-Freeman LE
BP
Bracci PM
BP
Brennan P
CF
Canzian F
DM
Du M
GS
Gallinger S
GG
Giles GG
GP
Goodman PJ
KC
Kooperberg C
LM
Le Marchand L
NR
Neale RE
SX
Shu XO
VK
Visvanathan K
WE
White E
ZW
Zheng W
AD
Albanes D
AG
Andreotti G
BA
Babic A
BW
Bamlet WR
BS
Berndt SI
BA
Blackford AL
BB
Bueno-de-Mesquita B
BJ
Buring JE
CD
Campa D
CS
Chanock SJ
CE
Childs EJ
DE
Duell EJ
FC
Fuchs CS
GJ
Gaziano JM
GE
Giovannucci EL
GM
Goggins MG
HP
Hartge P
HM
Hassan MM
HE
Holly EA
HR
Hoover RN
HR
Hung RJ
KR
Kurtz RC
LI
Lee IM
MN
Malats N
MR
Milne RL
NK
Ng K
OA
Oberg AL
PS
Panico S
PU
Peters U
PM
Porta M
RK
Rabe KG
RE
Riboli E
RN
Rothman N
SG
Scelo G
SH
Sesso HD
SD
Silverman DT
SV
Stevens VL
SO
Strobel O
TI
Thompson IM
TA
Tjonneland A
TA
Trichopoulou A
VD
Van Den Eeden SK
WJ
Wactawski-Wende J
WN
Wentzensen N
WL
Wilkens LR
YH
Yu H
YF
Yuan F
ZA
Zeleniuch-Jacquotte A
AL
Amundadottir LT
LD
Li D
JE
Jacobs EJ
PG
Petersen GM
WB
Wolpin BM
RH
Risch HA
KP
Kraft P
CN
Chatterjee N
KA
Klein AP
SR
Stolzenberg-Solomon R
Chapter II

Abstract

Summary of the research findings

Germline variation and smoking are independently associated with pancreatic ductal adenocarcinoma (PDAC). We conducted genome-wide smoking interaction analysis of PDAC using genotype data from four previous genome-wide association studies in individuals of European ancestry (7,937 cases and 11,774 controls). Examination of expression quantitative trait loci data from the Genotype-Tissue Expression Project followed by colocalization analysis was conducted to determine whether there was support for common SNP(s) underlying the observed associations. Statistical tests were two sided and P < 5 × 10-8 was considered statistically significant. Genome-wide significant evidence of qualitative interaction was identified on chr2q21.3 in intron 5 of the transmembrane protein 163 (TMEM163) and upstream of the cyclin T2 (CCNT2). The most significant SNP using the Empirical Bayes method, in this region that included 45 significantly associated SNPs, was rs1818613 [per allele OR in never smokers 0.87, 95% confidence interval (CI), 0.82-0.93; former smokers 1.00, 95% CI, 0.91-1.07; current smokers 1.25, 95% CI 1.12-1.40, P interaction = 3.08 × 10-9). Examination of the Genotype-Tissue Expression Project data demonstrated an expression quantitative trait locus in this region for TMEM163 and CCNT2 in several tissue types. Colocalization analysis supported a shared SNP, rs842357, in high linkage disequilibrium with rs1818613 (r 2 = 0. 94) driving both the observed interaction and the expression quantitative trait loci signals. Future studies are needed to confirm and understand the differential biologic mechanisms by smoking status that contribute to our PDAC findings. SIGNIFICANCE: This large genome-wide interaction study identifies a susceptibility locus on 2q21.3 that significantly modified PDAC risk by smoking status, providing insight into smoking-associated PDAC, with implications for prevention.

7,937 European ancestry cases, 11,774 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

19711
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

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