The CYP17 gene encodes the cytochrome P450c17 alpha enzyme, which functions
at 2 different points in the steroid biosynthesis pathway, and is consider
ed a candidate susceptibility gene for endocrine-related tumors. A T to C s
ubstitution polymorphism exists in the 5' promoter region of this gene, and
creates an additional Sp I-type motif. Several studies have examined this
polymorphism as a risk factor for breast cancer, but results have been conf
licting. We examined 319 cases of ovarian cancer and 298 unaffected control
s for the T-C polymorphism, There was no significant difference between cas
es and controls for the allele frequencies (p = 0.6), or for genotype distr
ibution (p = 0.9). The odds ratio (95% confidence interval) for ovarian can
cer was 1.13 (0.70-1.82) for the putative "cancer susceptibility" CC genoty
pe and 1.07 (0.77-1.48) for any C allele (CC or CT genotype), Results were
little different after adjustment for age. Stratification of the ovarian ca
ncer cases according to form (benign, low malignant potential or invasive),
histology, grade or stage failed to reveal any heterogeneity with respect
to CYP17 genotype. Our data provide no evidence for an association between
ovarian cancer risk and the genotype defined by the CYP175' promoter region
T-C polymorphism, (C) 2000 Wiley-Liss, Inc.