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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/17904


    Title: Mitotic arrest induced in human DU145 prostate cancer cells in response to KHC-4 treatment
    Authors: Shen, Cheng-Huang
    Lin, Tien-Huang
    Hsieh, You-Liang
    Shen, Chia-Yao
    Kuo, Sheng-Chu
    Wu, Hsi-Chin
    Chien, Wen-Shin
    Hsieh, Dennis Jine-Yuan
    Wen, Su-Ying
    Ting, Wei-Jen
    Yao, Chun-Hsu
    Huang, Chih-Yang
    Contributors: 中山醫大
    Keywords: KHC-4;DU145 cells;antiproliferation;cell cycle arrest;cell migration;inhibition
    Date: 2015
    Issue Date: 2017-06-30T09:40:59Z (UTC)
    ISSN: 1520-4081
    Abstract: Abstract

    In this study, the antitumor activity of KHC-4 was analyzed using human prostate cancer (CaP) cells and the underlining anticancer mechanisms of KHC-4 were identified. KHC-4 inhibited cell proliferation and induced cytotoxicity in the castration-resistant CaP DU145 cell line. The most effective concentration of KHC-4 was 0.1 μM. Cell cycle analysis demonstrated that KHC-4 treatment caused G2/M arrest and a subsequent increase in the sub-G1 population. Furthermore, KHC-4 is up-regulated p21, p27, and p53 in a time- and concentration-dependent manner. The exposure of cells to KHC-4 induced Cdk1/cyclin B1 complex activity, which led to cell cycle arrest. Moreover, KHC-4 inhibited the activities of MMP-2 and MMP-9 to inhibit tumor cell metastasis. © 2015 Wiley Periodicals, Inc. Environ Toxicol 31: 1879–1887, 2016.
    URI: http://dx.doi.org/10.1002/tox.22189
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/17904
    Relation: Environ Toxicol. 2015 Aug 25.
    Appears in Collections:[醫學系] 期刊論文

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