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Vol. 284, Issue 3, 1197-1202, March 1998
Center for Experimental Therapeutics (W-C.S., Y.Q.), University of
Pennsylvania School of Medicine, Philadelphia, Pennsylvania and
In
Vitro Technologies Inc. (A.P.L.), University of Maryland Technology
Center, Baltimore, Maryland
Estrogen sulfotransferase (EST) catalyzes the specific sulfonation of
estrogen at the 3
-hydroxyl position using
3
-phosphoadenosine-5
-phosphosulfate as an activated sulfate donor.
Sulfonation renders the hormone biologically inactive as well as
changing its half-life within the human body. Studies in the rat and
mouse have suggested that expression of EST in the liver is age- and
sex-dependent, being prominent only in sexually mature young males.
Although a human EST cDNA has previously been cloned, the
characteristics of hepatic EST expression in human subjects remain to
be defined. In this study, we have investigated and compared the
expression of EST in 10 human liver samples by using an EST-specific
antibody and performing enzyme activity assays. We found a marked
interindividual variation (up to 25-fold) in the hepatic expression of
EST. However, EST protein level in the human liver is correlated
neither with gender nor with age. Interestingly, paired-group analysis
revealed a statistically significant difference in the hepatic
expression of EST protein and activity between alcohol users and
nonusers. We conclude that, unlike what is observed in the rodent
liver, EST expression in the human liver is not sex-limited. Thus
hepatic EST may play a role in estrogen metabolism and homeostasis in both genders of human subjects. The marked individual variation suggests that EST gene expression is subject to sensitive control by
genetic or environmental factors. The potential correlation between
alcohol consumption and hepatic EST expression deserves further
evaluation.
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