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    PI3K/Akt/mTOR pathway dual inhibitor BEZ235 suppresses the stemness of colon cancer stem cells

    Access Status
    Fulltext not available
    Authors
    Chen, J.
    Shao, R.
    Li, F.
    Monteiro, M.
    Liu, Jian
    Xu, Z.
    Gu, W.
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Chen, J. and Shao, R. and Li, F. and Monteiro, M. and Liu, J. and Xu, Z. and Gu, W. 2015. PI3K/Akt/mTOR pathway dual inhibitor BEZ235 suppresses the stemness of colon cancer stem cells. Clinical and Experimental Pharmacology and Physiology. 42 (12): pp. 1317-1326.
    Source Title
    Clinical and Experimental Pharmacology and Physiology
    DOI
    10.1111/1440-1681.12493
    ISSN
    0305-1870
    School
    WASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
    URI
    http://hdl.handle.net/20.500.11937/72938
    Collection
    • Curtin Research Publications
    Abstract

    © 2015 Wiley Publishing Asia Pty Ltd. Colon cancer is one of the most common cancers worldwide with high mortality. A major issue in colon cancer treatment is drug-resistance and metastasis that have been ascribed to the cancer stem cells. In this study, colon cancer stem cells were isolated through sphere culture and verified with the cancer stem cell markers CD133, CD44, and CD24. It was demonstrated that the PI3K/Akt/mTOR signalling pathway was highly activated in the colon cancer stem cells and that inhibition of the PI3K/Akt/mTOR pathway by the inhibitor BEZ235 suppressed the colon cancer stem cell proliferation with reduced stemness indicated by CD133 and Lgr5 expressions. Treatment with insulin as a known activator of the PI3K/Akt pathway increased CD133 expression and decreased the effects of BEZ235 on colon cancer proliferation and survival. The data presented here collectively suggest that the PI3K/Akt/mTOR pathway underpins the stemness of colon cancer stem cells and BEZ235 is potentially a good drug candidate for treatment of colon cancer drug resistance and metastasis.

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