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mTOR inhibitors in cancer therapy [version 1; referees: 3 approved]
- Source :
- F1000Research. 5:F1000 Faculty Rev-2078
- Publication Year :
- 2016
- Publisher :
- London, UK: F1000 Research Limited, 2016.
-
Abstract
- The mammalian target of rapamycin, mTOR, plays key roles in cell growth and proliferation, acting at the catalytic subunit of two protein kinase complexes: mTOR complexes 1 and 2 (mTORC1/2). mTORC1 signaling is switched on by several oncogenic signaling pathways and is accordingly hyperactive in the majority of cancers. Inhibiting mTORC1 signaling has therefore attracted great attention as an anti-cancer therapy. However, progress in using inhibitors of mTOR signaling as therapeutic agents in oncology has been limited by a number of factors, including the fact that the classic mTOR inhibitor, rapamycin, inhibits only some of the effects of mTOR; the existence of several feedback loops; and the crucial importance of mTOR in normal physiology.
Details
- ISSN :
- 20461402
- Volume :
- 5
- Database :
- F1000Research
- Journal :
- F1000Research
- Notes :
- Editorial Note on the Review Process F1000 Faculty Reviews are commissioned from members of the prestigious F1000 Faculty and are edited as a service to readers. In order to make these reviews as comprehensive and accessible as possible, the referees provide input before publication and only the final, revised version is published. The referees who approved the final version are listed with their names and affiliations but without their reports on earlier versions (any comments will already have been addressed in the published version). The referees who approved this article are: Joseph Avruch, Department of Molecular Biology, Massachusetts General Hospital, Boston, MA, USA No competing interests were disclosed. Andrew Tee, Institute of Cancer & Genetics, Cardiff University School of Medicine, Cardiff, UK No competing interests were disclosed. Mario Pende, Institut Necker-Enfants Malades, Inserm, Paris Descartes University, Paris, France No competing interests were disclosed., , [version 1; referees: 3 approved]
- Publication Type :
- Academic Journal
- Accession number :
- edsfor.10.12688.f1000research.9207.1
- Document Type :
- review
- Full Text :
- https://doi.org/10.12688/f1000research.9207.1