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dc.contributor.authorChen, J.
dc.contributor.authorShao, R.
dc.contributor.authorLi, F.
dc.contributor.authorMonteiro, M.
dc.contributor.authorLiu, Jian
dc.contributor.authorXu, Z.
dc.contributor.authorGu, W.
dc.date.accessioned2018-12-13T09:14:51Z
dc.date.available2018-12-13T09:14:51Z
dc.date.created2018-12-12T02:46:48Z
dc.date.issued2015
dc.identifier.citationChen, 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.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/72938
dc.identifier.doi10.1111/1440-1681.12493
dc.description.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.

dc.publisherWiley-Blackwell Publishing Asia
dc.titlePI3K/Akt/mTOR pathway dual inhibitor BEZ235 suppresses the stemness of colon cancer stem cells
dc.typeJournal Article
dcterms.source.volume42
dcterms.source.number12
dcterms.source.startPage1317
dcterms.source.endPage1326
dcterms.source.issn0305-1870
dcterms.source.titleClinical and Experimental Pharmacology and Physiology
curtin.departmentWASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
curtin.accessStatusFulltext not available


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