國家衛生研究院 NHRI:Item 3990099045/2740
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    題名: A novel peroxisome proliferator-activated receptor alpha/gamma agonist, BPR1H0101, inhibits topoisomerase II catalytic activity in human cancer cells
    作者: Kao, YH;Hsieh, HP;Chitlimalla, SK;Pan, WY;Kuo, CC;Tsai, YC;Lin, WH;Chuang, SE;Chang, JY
    貢獻者: National Institute of Cancer Research;Division of Biotechnology and Pharmaceutical Research
    摘要: Peroxisome proliferator-activated receptor (PPAR) gamma agonists are used clinically for treating diabetes mellitus and cancer. 2-Methyl-2[(1-{3-phenyl-7-propylbenzol[d]isoxazol-6-yl}oxy)propyl]-1 H-4-indolyl) oxy]propanoic acid (BPR1H0101) is a novel synthetic indole-based compound, discovered through research to identify new PPAR gamma agonists, and it acts as a dual agonist for PPAR gamma and PPAR alpha. Isobologram analysis demonstrated that BPR1H0101 is capable of antagonistic interaction with the topoisomerase (topo) II poison, VP16. A study of its mechanism showed that BPR1H0101 could inhibit the catalytic activity of topo II in vitro, but did not produce detectable topo II-mediated DNA strand breaks in human oral cancer KB cells. Furthermore, BPR1H0101 could inhibit VP16-induced topo II-mediated DNA cleavage and ataxia-telangiectasia-mutated phosphorylation in KB cells. The results suggest that BPR1H0101 can interfere with the topo II reaction by inhibiting catalytic activity before the formation of the intermediate cleavable complex; consequently, it can impede VP16-induced topo II-mediated DNA cleavage and cell death. This is the first identified PPAR alpha/gamma agonist that can serve as a topo II catalytic inhibitor, to interfere with VP16-induced cell death. The result might have relevance to the clinical use of the PPAR alpha/gamma agonist in combination chemotherapy.
    關鍵詞: Oncology;Pharmacology & Pharmacy
    日期: 2008-02
    關聯: Anti-Cancer Drugs. 2008 Feb;19(2):151-158.
    Link to: http://meta.wkhealth.com/pt/pt-core/template-journal/lwwgateway/media/landingpage.htm?an=00001813-200802000-00006
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0959-4973&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000252479900006
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=37849010055
    顯示於類別:[張俊彥] 期刊論文
    [謝興邦] 期刊論文
    [莊雙恩] 期刊論文
    [郭靜娟] 期刊論文

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