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Estrogen Regulation of c-fos Messenger Ribonucleic Acid

Open access
Loose-Mitchell, David S., Chiappetta, Constance, Stancel, George M.·1988·Molecular Endocrinology

Abstract

Acute administration of 17 beta-estradiol to immature female rats elicits a rapid and striking increase in the size of the uterus. This increase in size to caused by both hypertrophy and hyperplasia in the epithelial, stromal, and myometrial cells in the uterus. Previous studies have shown that induction of mRNA for the epidermal growth factor receptor, the cellular homolog of the erb-B oncogene, occurs early during estrogen-stimulated uterine growth. We report here that estradiol causes a very rapid induction of the mRNA for the cellular oncogene c-fos in immature rat uterus. Steady state levels of c-fos mRNA reach a maximum 3 h after 17 beta-estradiol administration and slowly return to low basal levels in 15 h. Dexamethasone, progesterone, and 5 alpha-dihydrotestosterone had no effect on uterine c-fos mRNA expression. The induction of c-fos mRNA by estrogen was unaffected by the protein synthesis inhibitor puromycin but completely abolished by the RNA synthesis inhibitor actinomycin D.

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Metadata

Authors
Loose-Mitchell, D. S., Chiappetta, C., & Stancel, G. M.
Venue
Molecular Endocrinology
Published
1988-10
Volume
2
Issue
10
Pages
946-951
ISSN
  • 0888-8809 (ISSN-L)
  • 1944-9917
OpenAlex
W2062543439
Cited by
201
References
0
FWCI
5.89
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Estrogen Regulation of c-fos Messenger Ribonucleic Acid. https://app.cochat.ai/papers/10.1210/mend-2-10-946
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Loose-Mitchell, D. S., Chiappetta, C., & Stancel, G. M. (1988). Estrogen Regulation of c-fos Messenger Ribonucleic Acid. Molecular Endocrinology. https://doi.org/10.1210/mend-2-10-946

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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