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- W1525899559 endingPage "66" @default.
- W1525899559 startingPage "49" @default.
- W1525899559 abstract "// Maria Giovanna Francipane 1,2 and Eric Lagasse 1 1 McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. 2 Ri.MED Foundation, Palermo, Italy. Correspondence: Eric Lagasse, email: // Keywords : mTOR, colorectal cancer, cancer stem-like cells, personalized medicine. Received : October 28, 2013 Accepted : December 3, 2013 Published : December 5, 2013 Abstract The mammalian target of rapamycin (mTOR) has emerged as a potential target for drug development, particularly due to the fact that it plays such a crucial role in cancer biology. In addition, next-generation mTOR inhibitors have become available, marking an exciting new phase in mTOR-based therapy. However, the verdict on their therapeutic effectiveness remains unclear. Here we review phosphatidylinositol-3-kinase (PI3K)/Akt/mTOR signaling as one of the primary mechanisms for sustaining tumor outgrowth and metastasis, recent advances in the development of mTOR inhibitors, and current studies addressing mTOR activation/inhibition in colorectal cancer (CRC). We will also discuss our recent comparative study of different mTOR inhibitors in a population of colon cancer stem cells (CSCs), and current major challenges for achieving individualized drug therapy using kinase inhibitors." @default.
- W1525899559 created "2016-06-24" @default.
- W1525899559 creator A5000371170 @default.
- W1525899559 creator A5000371607 @default.
- W1525899559 date "2013-12-05" @default.
- W1525899559 modified "2023-10-16" @default.
- W1525899559 title "mTOR pathway in colorectal cancer: an update" @default.
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