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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11262


    Title: Apoptotic and anti-proliferative effects of 17β-estradiol and 17β-estradiol-like compounds in the Hep3B cell line
    Authors: Huang, Erh-Jung
    Wu, Cheng-Chung
    Huang, Hsien-Ping
    Liu, Jer-Yuh
    Lin, Chung-Sheng
    Chang, Yan-Zin
    James, A.Lin
    Lin, Jaung-Geng
    Chen, Li-Mien
    Lee, Shin-Da
    Kuo, Wei-Wen
    Huang, Chih-Yang
    Contributors: 中山醫學大學
    Keywords: hepatocellular carcinoma (HCC);17 β-estrodiol;17 β-estrodiol-like compounds;apoptotic and antiproliferative effects
    Date: 2006
    Issue Date: 2015-07-15T04:39:11Z (UTC)
    ISSN: 0300-8177
    Abstract: Since there is evidence for estrogen and estrogen-like compounds to have beneficial effect on the pathogenesis of hepatocellular carcinoma (HCC), this study was designed to investigative the apoptotic and anti-proliferative effects of these compounds on the human hepatoma Hep3B cell line. The Hep3B cells were treated with 17β-estradiol (E2), diethylstilbestrol (DES), tamoxifen, and genistein. After treatments of these compounds at the concentration of 10-6 or 10-8 M, the Hep3B cells were demonstrated to have significant DNA fragmentation, nucleus condensation, cytochrome-c leaking from the mitochondria and caspase-3 activation by DAPI and Western blotting. The cells were also observed to have declined proliferative potential by MTT assay, arrested cell cycle by flow-cytometry measurements. However, the cytochrome-c leaking from the mitochondria induced by E2 and E2-like compounds was blocked totally by ICI 182,780 treatment. These finding suggest that estrogen and the estrogen-like compounds may induce anti-proliferative and apoptotic effects in Hep3B cells, and the E2 and the E2-like compounds mediated apoptotic effect was estrogen receptor dependent. Among the drugs tested, E2, E2 agonists (DES and genistein) and partial antagonist (tamoxifen), all showed the stronger anti-tumor potential.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11262
    http://dx.doi.org/10.1007/s11010-005-9000-y
    Relation: Molecular and Cellular Biochemistry October 2006, Volume 290, Issue 1-2, pp 1-7
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