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    Targeting TNF-related apoptosis-inducing ligand (TRAIL) receptor by natural products as a potential therapeutic approach for cancer therapy

    Access Status
    Fulltext not available
    Authors
    Dai, X.
    Zhang, J.
    Arfuso, Frank
    Chinnathambi, A.
    Zayed, M.
    Alharbi, S.
    Kumar, A.
    Ahn, K.
    Sethi, G.
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Dai, X. and Zhang, J. and Arfuso, F. and Chinnathambi, A. and Zayed, M. and Alharbi, S. and Kumar, A. et al. 2015. Targeting TNF-related apoptosis-inducing ligand (TRAIL) receptor by natural products as a potential therapeutic approach for cancer therapy. Experimental Biology and Medicine. 240 (6): pp. 760-773.
    Source Title
    Experimental Biology and Medicine
    DOI
    10.1177/1535370215579167
    ISSN
    1535-3702
    School
    School of Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/5659
    Collection
    • Curtin Research Publications
    Abstract

    © 2015 by the Society for Experimental Biology and Medicine Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) has been shown to selectively induce apoptotic cell death in various tumor cells by engaging its death-inducing receptors (TRAIL-R1 and TRAIL-R2). This property has led to the development of a number of TRAIL–receptor agonists such as the soluble recombinant TRAIL and agonistic antibodies, which have shown promising anticancer activity in preclinical studies. However, besides activating caspase-dependent apoptosis in several cancer cells, TRAIL may also activate nonapoptotic signal transduction pathways such as nuclear factor-kappa B, mitogen-activated protein kinases, AKT, and signal transducers and activators of transcription 3, which may contribute to TRAIL resistance that is being now frequently encountered in various cancers. TRAIL resistance can be overcome by the application of efficient TRAIL-sensitizing pharmacological agents. Natural compounds have shown a great potential in sensitizing cells to TRAIL treatment through suppression of distinct survival pathways. In this review, we have summarized both apoptotic and nonapoptotic pathways activated by TRAIL, as well as recent advances in developing TRAIL–receptor agonists for cancer therapy. We also briefly discuss combination therapies that have shown great potential in overcoming TRAIL resistance in various tumors.

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