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    Molecular Targets of Ascochlorin and Its Derivatives for Cancer Therapy

    Access Status
    Fulltext not available
    Authors
    Min-Wen, J.
    Yan-Jiang, B.
    Mishra, S.
    Dai, X.
    Magae, J.
    Shyh-Chang, N.
    Kumar, Alan Prem
    Sethi, G.
    Date
    2017
    Type
    Journal Article
    
    Metadata
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    Citation
    Min-Wen, J. and Yan-Jiang, B. and Mishra, S. and Dai, X. and Magae, J. and Shyh-Chang, N. and Kumar, A.P. et al. 2017. Molecular Targets of Ascochlorin and Its Derivatives for Cancer Therapy. Advances in Protein Chemistry and Structural Biology. 108: pp. 199-225.
    Source Title
    Advances in Protein Chemistry and Structural Biology
    DOI
    10.1016/bs.apcsb.2017.01.001
    ISSN
    1876-1623
    School
    Curtin Medical School
    URI
    http://hdl.handle.net/20.500.11937/62609
    Collection
    • Curtin Research Publications
    Abstract

    © 2017 Elsevier Inc. Cancer is an extremely complex disease comprising of a multitude of characteristic hallmarks that continue to evolve with time. At the genomic level, random mutations leading to deregulation of diverse oncogenic signal transduction cascades and polymorphisms coupled with environmental as well as life style-related factors are major causative agent contributing to chemoresistance and the failure of conventional therapies as well as molecular targeted agents. Hence, there is an urgent need to identify novel alternative therapies based on alternative medicines to combat this dreaded disease. Ascochlorin (ASC), an isoprenoid antibiotic isolated initially from the fermented broth of Ascochyta viciae, and its synthetic derivatives have recently demonstrated substantial antineoplastic effects in a variety of tumor cell lines and mouse models. The major focus of this review article is to briefly analyze the chemopreventive as well as therapeutic properties of ASC and its derivatives and to identify the multiple molecular targets modulated by this novel class of anticancer agent.

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