國家衛生研究院 NHRI:Item 3990099045/12034
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/12034


    Title: Toward understanding the antitumor effects of water-soluble fullerene derivatives on lung cancer cells: Apoptosis or autophagy pathways?
    Authors: Wong, CW;Zhilenkov, AV;Kraevaya, OA;Mischenko, DV;Troshin, PA;Hsu, SH
    Contributors: Institute of Cellular and Systems Medicine
    Abstract: Here we report the synthesis and investigation of anticancer effects of a series of water-soluble fullerene derivatives bearing amino acid (F1-F7) and thioacid (F8-F10) residues. Compounds F4 and F10 efficiently inhibited proliferation of lung cancer cells in vitro while being nontoxic to endothelial cells. It was revealed that the cancer cell death was caused by either autophagy (F4) or apoptosis (F10). Both fullerene derivatives strongly inhibited the tumor growth in the zebrafish xenograft model. In contrast to the vast majority of known cytostatics, fullerene derivatives do not show any significant acute toxicity effects in mice. Importantly, functional groups attached to the carbon cage affect interaction of the compounds with cancer cells, thus enabling realization of two different cell death mechanisms. The obtained results pave a way to the development of a new generation of selective antitumor drugs suppressing efficiently the proliferation of cancer cells while being nontoxic to normal cells.
    Date: 2019-07-30
    Relation: Journal of Medicinal Chemistry. 2019 Jul 30;62(15):7111-7125.
    Link to: http://dx.doi.org/10.1021/acs.jmedchem.9b00652
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0022-2623&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000480500600019
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85071191557
    Appears in Collections:[Shan-Hui Hsu] Periodical Articles

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