Abstract | BACKGROUND & OBJECTIVE: METHODS:
ERalpha-positive cell line Ishikawa and ERalpha-negative cell line HEC-IA were treated with different concentrations of 17beta-E(2) (1x10(-10) mol/L, 1x10(-8) mol/L, and 1x10(-6) mol/L) for 24 h and 48 h, respectively. The levels of ERRalpha mRNA and protein were examined by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot. 17beta-E(2) (1x10(-8) mol/L) and complete ER inhibitor ICI182,780 (1x10(-6) mol/L) were given concomitantly to observe the change of ERRalpha expression. RESULTS: The levels of ERRalpha mRNA and protein in Ishikawa cells were down-regulated after stimulated for 24 h and 48 h by different concentrations of 17beta-E(2). The maximal effect was observed at the concentration of 1x10(-8) mol/L. When 17beta-E(2) and ICI182,780 were given simultaneously to Ishikawa cells, this down-regulation was blocked. However, the level of ERRalpha mRNA, not protein, in HEC-IA cells was up-regulated after stimulated by different concentrations of 17beta-E(2) for 24 h. After stimulated by 17beta-E(2) for 48 h, the level of ERRalpha protein was up-regulated, which could not be blocked by ICI182,780. CONCLUSIONS: 17beta-E(2) can down-regulate the expression of ERRalpha in Ishikawa cells, which is mediated by ERalpha. 17beta-E(2) can up-regulate the expression of ERRalpha in HEC-IA cells, but this regulation cannot be blocked by ICI182,780.
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Authors | Min Gao, Peng-Ming Sun, Dan Zhao, Jian-Liu Wang, Xiao-Ping Li, Li-Hui Wei |
Journal | Ai zheng = Aizheng = Chinese journal of cancer
(Ai Zheng)
Vol. 25
Issue 5
Pg. 538-42
(May 2006)
China |
PMID | 16687070
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- ERRalpha estrogen-related receptor
- Estrogen Antagonists
- Estrogen Receptor alpha
- RNA, Messenger
- Receptors, Estrogen
- Fulvestrant
- Estradiol
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Topics |
- Cell Line, Tumor
- Dose-Response Relationship, Drug
- Endometrial Neoplasms
(chemistry, genetics, metabolism, pathology)
- Estradiol
(administration & dosage, analogs & derivatives, pharmacology)
- Estrogen Antagonists
(pharmacology)
- Estrogen Receptor alpha
(analysis, physiology)
- Female
- Fulvestrant
- Gene Expression Regulation, Neoplastic
- Humans
- RNA, Messenger
(metabolism)
- Receptors, Estrogen
(biosynthesis, genetics)
- Signal Transduction
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