TY - JOUR
T1 - Estrogen regulation of epidermal growth factor receptor messenger ribonucleic acid
AU - Lingham, Russell B.
AU - Stancel, George M.
AU - Loose-Mitchell, David S.
PY - 1988/3
Y1 - 1988/3
N2 - Previous studies have demonstrated that 17 β-estra-diol (E2) causes a 3-fold increase in epidermal growth factor (EGF) receptors in uterine membranes. We now report that the increase in uterine EGF receptor levels is due to an increase in the steady-state levels of EGF receptor mRNA. After a single E2 injection, EGF receptor mRNA levels, as determined by RNA blots, increase 3- to 4-fold between 1 and 3 h, remain elevated at 6 h, and decline between 12 and 18 h. The effect is specific for E2 since the nonestrogenic hormones progesterone, dexamethasone, 5 α-dihydrotestosterone, and the inactive stereoisomer of E2, 17α-estradiol, are without effect. E2-Mediated increases in EGF receptor mRNA levels are blocked by actinomycin D but not by puromycin. Taken together, these results indicate that E2 regulates the level of EGF receptor by increasing the steady-state concentration of EGF receptor mRNA in vivo.
AB - Previous studies have demonstrated that 17 β-estra-diol (E2) causes a 3-fold increase in epidermal growth factor (EGF) receptors in uterine membranes. We now report that the increase in uterine EGF receptor levels is due to an increase in the steady-state levels of EGF receptor mRNA. After a single E2 injection, EGF receptor mRNA levels, as determined by RNA blots, increase 3- to 4-fold between 1 and 3 h, remain elevated at 6 h, and decline between 12 and 18 h. The effect is specific for E2 since the nonestrogenic hormones progesterone, dexamethasone, 5 α-dihydrotestosterone, and the inactive stereoisomer of E2, 17α-estradiol, are without effect. E2-Mediated increases in EGF receptor mRNA levels are blocked by actinomycin D but not by puromycin. Taken together, these results indicate that E2 regulates the level of EGF receptor by increasing the steady-state concentration of EGF receptor mRNA in vivo.
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U2 - 10.1210/mend-2-3-230
DO - 10.1210/mend-2-3-230
M3 - Article
C2 - 3398852
AN - SCOPUS:0023880121
SN - 0888-8809
VL - 2
SP - 230
EP - 235
JO - Molecular Endocrinology
JF - Molecular Endocrinology
IS - 3
ER -