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ABSTRACT: Association Between Sulfotransferase 1A1 Genotype and
Survival of Breast Cancer Patients Receiving Tamoxifen Therapy
Background: Human sulfotransferase 1A1 (SULT1A1) catalyzes the
sulfation of a variety of phenolic and estrogenic compounds,
including 4-hydroxytamoxifen (4-OH TAM), the active metabolite
of tamoxifen. A functional polymorphism in exon 7 of the SULT1A1
gene (SULT1A1*2) has been described that generates an enzyme
that has approximately twofold lower activity and is less thermostable
than that of the common allele SULT1A1*1.
We investigated the
hypothesis that that high sulfation activity would increase the
elimination of 4-OH TAM by examining whether the presence of
this polymorphism affects the efficacy of tamoxifen therapy.
Methods: We examined the relationship between the SULT1A1*2 allele
and survival in a cohort of 337 women with breast cancer who
received tamoxifen (n = 160) or who did not (n = 177). SULT1A1
genotype was determined by restriction fragment polymorphism
analysis. Patient survival was evaluated according to SULT1A1
genotype using Kaplan-Meier survival functions. Hazard ratios
(HRs) were calculated from adjusted Cox proportional hazards
modeling. All statistical tests were two-sided.
Results: Among tamoxifen-treated patients, those who were homozygous
for the SULT1A1*2 low-activity allele had approximately three times
the risk of death (HR = 2.9, 95% confidence interval [CI] = 1.1 to
7.6) as those who were homozygous for the common allele or those
who were heterozygous (SULT1A1*1/*2).
Among patients who did
not receive tamoxifen, there was no association between survival
and SULT1A1 genotype (HR = 0.7, 95% CI = 0.3 to 1.5).
Conclusions: Sulfation of 4-OH TAM provides a previously unanticipated
benefit, possibly due to alterations in the bioavailability of the active
metabolite or to undefined estrogen receptor-mediated events.
These data alternatively suggest that variability in the metabolism
of tamoxifen may affect its efficacy.
[11/06/2002; Journal of the National Cancer Institute]
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