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Vanderbilt-Ingram Cancer Center and Vanderbilt Center for Health Services Research, Vanderbilt University, Nashville, Tennessee 37232-8300 [W. Z., W. W.]; School of Public Health, University of South Carolina, Columbia, South Carolina [D. X.]; Mayo Clinic Cancer Center, Rochester, Minnesota 55905 [J. R. C., T. A. S.]; and School of Public Health, University of Minnesota, Minneapolis, Minnesota 55454 [A. R. F.]
Sulfotransferase (SULT) 1A1 is involved in the inactivation of estrogens
and bioactivation of heterocyclic amines and polycyclic aromatic
hydrocarbons. A G
A transition at codon 213 (CGC/Arg
to CAC/His) of the SULT1A1 gene
was reported recently, and individuals homozygous for the
His allele have a substantially lower activity of this
enzyme than those with other genotypes. We hypothesized that the
His allele may be a risk factor for breast cancer,
particularly among women who had risk factors related to higher
endogenous estrogen exposure. This hypothesis was investigated in a
case-control study conducted in a cohort of postmenopausal Iowa women
who completed a mailed questionnaire in 1986 on lifestyle factors
including information on major breast cancer risk factors. DNA samples
and information related to well-done meat intake were obtained from
breast cancer cases diagnosed between 1992 and 1994 and a random sample
of cancer-free cohort members. Multivariate analysis was performed on
data from 156 cases and 332 controls who donated a blood sample. The
frequency of the His allele was 41.6% in cases and
34.1% in controls (P = 0.03), and the risk of
breast cancer was increased with the number of His
alleles (P for trend = 0.02). Compared with women
with the Arg/Arg genotype, an 80% elevated risk was
observed among women homozygous for the His allele (95%
confidence interval, 1.03.2; P = 0.04). This
positive association was more pronounced among women who drank alcohol
and had a high body mass index, early age at menarche, and late age at
menopause, factors related to high endogenous estrogen exposure, than
among those who did not have these risk factors. The risk of breast
cancer was elevated with increasing doneness level of red meat intake
among women with the Arg/Arg genotype (P
for trend, 0.01) or the Arg/His genotype
(P for trend, 0.10), whereas this association was not
evident for women with the His/His genotype. The results
from this study suggest that homozygosity for the SULT1A1
His213 allele may be a risk factor for breast
cancer, and its effect may be modified by the exposure level of
endogenous estrogens and heterocyclic amines.
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