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[Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines]

[Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines] Research Abstract Details 

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  • [Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines] Abstract Text:

    min gaoMin Gao,peng-ming sunPeng-Ming Sun,dan zhaoDan Zhao,jian-liu wangJian-Liu Wang,xiao-ping liXiao-Ping Li,li-hui weiLi-Hui Wei,

    BACKGROUND & OBJECTIVE: Estrogen receptor-related receptor alpha (ERRalpha), a member of the subfamily of orphan nuclear receptors, could compete with estrogen receptor alpha (ERalpha) to bind the same target genes and interfere in ER signal pathway. Therefore, it might be associated to the tumorigenesis of endometrial carcinoma. This study was to explore the regulatory effect of 17beta-estradiol (17beta-E(2)) on ERRalpha expression, and to elucidate the relationship between ERRalpha and ER signal pathway in endometrial carcinoma cell lines. 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.

    [Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines] Publishing Authors By Initials

    m gaoM Gao,pm sunPM Sun,d zhaoD Zhao,jl wangJL Wang,xp liXP Li,lh weiLH Wei,

    For similar abstracts research abstracts see: abstracts research

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    [Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines] Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Ai zheng = Aizheng = Chinese journal of cancer

    VOLUME: 25

    Page Numbers: 538-42

    Journal Abbreviation: Ai Zheng

    ISSN: 1000-467X

    DAY: 11

    MONTH: May

    YEAR: 2006

    [Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines] Information

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    LANGUAGE: chi

    NlmUniqueID: 9424852

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    Grant and Affiliation Information for [Regulatory effect of 17beta-estradiol on expression of orphan nuclear receptor ERRalpha in endometrial carcinoma cell lines]

    AFFILIATION: Department of Gynecology, Peopleos Hospital, Peking University, Beijing, 100044, P. R. China.

    Country: China

    China Research PublicationChina Research Publication

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    MEDLINETA: Ai Zheng

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