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Vol. 31, Issue 1, 1-6, January 2003
Dept of Biochemistry (V.V.), CYP3A4, a cytochrome P450 (P450) isoform metabolizes
estrogens, whereas CYP3A7, a fetal liver P450 isoform, is involved in estriol biosynthesis. The goal of this study was to evaluate expression of these enzymes in human uterine tissue during the proliferative and
secretory phases of the menstrual cycle. Endometrium and cervix specimens were collected from women undergoing hysterectomy
(n = 36). Total mRNA was extracted, quantified, and
reverse-transcription polymerase chain reaction (RT-PCR) was
carried out using consensus primers for CYP3A. The 453 base pairs PCR
product was hybridized with specific internal oligonucleotide probes
for CYP3A4 or CYP3A7 end labeled with 32P
Dept of Obstetrics and
Gynecology,
Health Sciences Center (D.D.G.),
West Virginia
University School
of Medicine,
Morgantown, West
Virginia;
Virginia Commonwealth University
School of Pharmacy
(M.A.S.),
School of Medicine, Medical College
of Virginia
Campus (S.G.),
Richmond, Virginia
-ATP. The
relative intensity of hybridization was determined by autoradiography.
Expression of CYP3A7 in endometrium was significantly greater
(~10-fold) in the proliferative phase compared with the secretory
phase (p < 0.05). CYP3A4 expression was comparable
between the two phases. Expression of both enzymes was minimal in the cervix. Fluorescence in situ hybridization of paraffinized sections indicated localized expression of CYP3A enzymes in the glandular epithelium as well as the stroma. Comparison of relative fluorescence intensity indicated differential expression of CYP3A7 in various phases
of the menstrual cycle. These results suggest that CYP3A expression in
the endometrium of premenopausal women may vary depending on the
menstrual cycle phase.
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