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GWAS Study

Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women.

Grant DJ, Manichaikul A, Alberg AJ et al.

31001917 PubMed ID
GWAS Study Type
1990 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

GD
Grant DJ
MA
Manichaikul A
AA
Alberg AJ
BE
Bandera EV
BJ
Barnholtz-Sloan J
BM
Bondy M
CM
Cote ML
FE
Funkhouser E
MP
Moorman PG
PL
Peres LC
PE
Peters ES
SA
Schwartz AG
TP
Terry PD
WX
Wang XQ
KT
Keku TO
HC
Hoyo C
BA
Berchuck A
SD
Sandler DP
TJ
Taylor JA
OK
O'Brien KM
VE
Velez Edwards DR
ET
Edwards TL
BA
Beeghly-Fadiel A
WN
Wentzensen N
PC
Pearce CL
WA
Wu AH
WA
Whittemore AS
MV
McGuire V
SW
Sieh W
RJ
Rothstein JH
MF
Modugno F
NR
Ness R
MK
Moysich K
RM
Rossing MA
DJ
Doherty JA
ST
Sellers TA
PJ
Permuth-Way JB
MA
Monteiro AN
LD
Levine DA
SV
Setiawan VW
HC
Haiman CA
LL
LeMarchand L
WL
Wilkens LR
KB
Karlan BY
MU
Menon U
RS
Ramus S
GS
Gayther S
GA
Gentry-Maharaj A
TK
Terry KL
CD
Cramer DW
GE
Goode EL
LM
Larson MC
KS
Kaufmann SH
CR
Cannioto R
OK
Odunsi K
EJ
Etter JL
HR
Huang RY
BM
Bernardini MQ
TA
Tone AA
MT
May T
GM
Goodman MT
TP
Thompson PJ
CM
Carney ME
TS
Tworoger SS
PE
Poole EM
LD
Lambrechts D
VI
Vergote I
VA
Vanderstichele A
VN
Van Nieuwenhuysen E
AH
Anton-Culver H
ZA
Ziogas A
BJ
Brenton JD
BL
Bjorge L
SH
Salvensen HB
KL
Kiemeney LA
ML
Massuger LFAG
PT
Pejovic T
BA
Bruegl A
MM
Moffitt M
CL
Cook L
LN
Le ND
BA
Brooks-Wilson A
KL
Kelemen LE
PP
Pharoah PDP
SH
Song H
CI
Campbell I
ED
Eccles D
DA
DeFazio A
KC
Kennedy CJ
SJ
Schildkraut JM
Chapter II

Abstract

Summary of the research findings

An association between genetic variants in the vitamin D receptor (VDR) gene and epithelial ovarian cancer (EOC) was previously reported in women of African ancestry (AA). We sought to examine associations between genetic variants in VDR and additional genes from vitamin D biosynthesis and pathway targets (EGFR, UGT1A, UGT2A1/2, UGT2B, CYP3A4/5, CYP2R1, CYP27B1, CYP24A1, CYP11A1, and GC). Genotyping was performed using the custom-designed 533,631 SNP Illumina OncoArray with imputation to the 1,000 Genomes Phase 3 v5 reference set in 755 EOC cases, including 537 high-grade serous (HGSOC), and 1,235 controls. All subjects are of African ancestry (AA). Logistic regression was performed to estimate odds ratios (OR) and 95% confidence intervals (CI). We further evaluated statistical significance of selected SNPs using the Bayesian False Discovery Probability (BFDP). A significant association with EOC was identified in the UGT2A1/2 region for the SNP rs10017134 (per allele OR = 1.4, 95% CI = 1.2-1.7, P = 1.2 × 10-6 , BFDP = 0.02); and an association with HGSOC was identified in the EGFR region for the SNP rs114972508 (per allele OR = 2.3, 95% CI = 1.6-3.4, P = 1.6 × 10-5 , BFDP = 0.29) and in the UGT2A1/2 region again for rs1017134 (per allele OR = 1.4, 95% CI = 1.2-1.7, P = 2.3 × 10-5 , BFDP = 0.23). Genetic variants in the EGFR and UGT2A1/2 may increase susceptibility of EOC in AA women. Future studies to validate these findings are warranted. Alterations in EGFR and UGT2A1/2 could perturb enzyme efficacy, proliferation in ovaries, impact and mark susceptibility to EOC.

755 African American cases, 1,235 African American controls

Chapter III

Study Statistics

Key metrics and study information

1990
Total Participants
GWAS
Study Type
No
Replicated
African American or Afro-Caribbean
Ancestry
Belgium, Norway, U.K., Canada, U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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