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GWAS Study

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types.

Kar SP, Beesley J, Amin Al Olama A et al.

27432226 PubMed ID
GWAS Study Type
228770 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

KS
Kar SP
BJ
Beesley J
AA
Amin Al Olama A
MK
Michailidou K
TJ
Tyrer J
KZ
Kote-Jarai Z
LK
Lawrenson K
LS
Lindstrom S
RS
Ramus SJ
TD
Thompson DJ
KA
Kibel AS
DA
Dansonka-Mieszkowska A
MA
Michael A
DA
Dieffenbach AK
GA
Gentry-Maharaj A
WA
Whittemore AS
WA
Wolk A
MA
Monteiro A
PA
Peixoto A
KA
Kierzek A
CA
Cox A
RA
Rudolph A
GA
Gonzalez-Neira A
WA
Wu AH
LA
Lindblom A
SA
Swerdlow A
ZA
Ziogas A
EA
Ekici AB
BB
Burwinkel B
KB
Karlan BY
NB
Nordestgaard BG
BC
Blomqvist C
PC
Phelan C
MC
McLean C
PC
Pearce CL
VC
Vachon C
CC
Cybulski C
SC
Slavov C
SC
Stegmaier C
MC
Maier C
AC
Ambrosone CB
HC
Høgdall CK
TC
Teerlink CC
KD
Kang D
TD
Tessier DC
SD
Schaid DJ
SD
Stram DO
CD
Cramer DW
ND
Neal DE
ED
Eccles D
FD
Flesch-Janys D
ED
Edwards DR
WD
Wokozorczyk D
LD
Levine DA
YD
Yannoukakos D
SE
Sawyer EJ
BE
Bandera EV
PE
Poole EM
GE
Goode EL
KE
Khusnutdinova E
HE
Høgdall E
SF
Song F
BF
Bruinsma F
HF
Heitz F
MF
Modugno F
HF
Hamdy FC
WF
Wiklund F
GG
Giles GG
OH
Olsson H
WH
Wildiers H
UH
Ulmer HU
PH
Pandha H
RH
Risch HA
DH
Darabi H
SH
Salvesen HB
NH
Nevanlinna H
GH
Gronberg H
BH
Brenner H
BH
Brauch H
AH
Anton-Culver H
SH
Song H
LH
Lim HY
MI
McNeish I
CI
Campbell I
VI
Vergote I
GJ
Gronwald J
LJ
Lubiński J
SJ
Stanford JL
BJ
Benítez J
DJ
Doherty JA
PJ
Permuth JB
CJ
Chang-Claude J
DJ
Donovan JL
DJ
Dennis J
SJ
Schildkraut JM
SJ
Schleutker J
HJ
Hopper JL
KJ
Kupryjanczyk J
PJ
Park JY
FJ
Figueroa J
CJ
Clements JA
KJ
Knight JA
PJ
Peto J
CJ
Cunningham JM
PJ
Pow-Sang J
BJ
Batra J
CK
Czene K
LK
Lu KH
HK
Herkommer K
KK
Khaw KT
MK
Matsuo K
MK
Muir K
OK
Offitt K
CK
Chen K
MK
Moysich KB
AK
Aittomäki K
OK
Odunsi K
KL
Kiemeney LA
ML
Massuger LF
FL
Fitzgerald LM
CL
Cook LS
CL
Cannon-Albright L
HM
Hooning MJ
PM
Pike MC
BM
Bolla MK
LM
Luedeke M
TM
Teixeira MR
GM
Goodman MT
SM
Schmidt MK
RM
Riggan M
AM
Aly M
RM
Rossing MA
BM
Beckmann MW
MM
Moisse M
SM
Sanderson M
SM
Southey MC
JM
Jones M
LM
Lush M
HM
Hildebrandt MA
HM
Hou MF
SM
Schoemaker MJ
GM
Garcia-Closas M
BN
Bogdanova N
RN
Rahman N
LN
Le ND
ON
Orr N
WN
Wentzensen N
PN
Pashayan N
PP
Peterlongo P
GP
Guénel P
BP
Brennan P
PP
Paulo P
WP
Webb PM
BP
Broberg P
FP
Fasching PA
DP
Devilee P
WQ
Wang Q
CQ
Cai Q
LQ
Li Q
KR
Kaneva R
BR
Butzow R
KR
Kopperud RK
SR
Schmutzler RK
SR
Stephenson RA
MR
MacInnis RJ
HR
Hoover RN
WR
Winqvist R
NR
Ness R
MR
Milne RL
TR
Travis RC
BS
Benlloch S
OS
Olson SH
MS
McDonnell SK
TS
Tworoger SS
MS
Maia S
BS
Berndt S
LS
Lee SC
TS
Teo SH
TS
Thibodeau SN
BS
Bojesen SE
GS
Gapstur SM
KS
Kjær SK
PT
Pejovic T
TT
Tammela TL
DT
Dörk T
BT
Brüning T
WT
Wahlfors T
KT
Key TJ
ET
Edwards TL
MU
Menon U
HU
Hamann U
MV
Mitev V
KV
Kosma VM
SV
Setiawan VW
KV
Kristensen V
AV
Arndt V
VW
Vogel W
ZW
Zheng W
SW
Sieh W
BW
Blot WJ
KW
Kluzniak W
SX
Shu XO
GY
Gao YT
SF
Schumacher F
FM
Freedman ML
BA
Berchuck A
DA
Dunning AM
SJ
Simard J
HC
Haiman CA
SA
Spurdle A
ST
Sellers TA
HD
Hunter DJ
HB
Henderson BE
KP
Kraft P
CS
Chanock SJ
CF
Couch FJ
HP
Hall P
GS
Gayther SA
ED
Easton DF
CG
Chenevix-Trench G
ER
Eeles R
PP
Pharoah PD
LD
Lambrechts D
Chapter II

Abstract

Summary of the research findings

Breast, ovarian, and prostate cancers are hormone-related and may have a shared genetic basis, but this has not been investigated systematically by genome-wide association (GWA) studies. Meta-analyses combining the largest GWA meta-analysis data sets for these cancers totaling 112,349 cases and 116,421 controls of European ancestry, all together and in pairs, identified at P < 10(-8) seven new cross-cancer loci: three associated with susceptibility to all three cancers (rs17041869/2q13/BCL2L11; rs7937840/11q12/INCENP; rs1469713/19p13/GATAD2A), two breast and ovarian cancer risk loci (rs200182588/9q31/SMC2; rs8037137/15q26/RCCD1), and two breast and prostate cancer risk loci (rs5013329/1p34/NSUN4; rs9375701/6q23/L3MBTL3). Index variants in five additional regions previously associated with only one cancer also showed clear association with a second cancer type. Cell-type-specific expression quantitative trait locus and enhancer-gene interaction annotations suggested target genes with potential cross-cancer roles at the new loci. Pathway analysis revealed significant enrichment of death receptor signaling genes near loci with P < 10(-5) in the three-cancer meta-analysis.

62,533 European ancestry breast cancer female cases, 60,976 European ancestry controls, 15,437 European ancestry invasive epithelial ovarian cancer female cases, 30,845 European ancestry controls, 34,379 European ancestry prostate cancer male cases, 33,164 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

228770
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
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.