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mTOR inhibitors in cancer therapy

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...

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Detalles Bibliográficos
Autores principales: Xie, Jianling, Wang, Xuemin, Proud, Christopher G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007757/
https://www.ncbi.nlm.nih.gov/pubmed/27635236
http://dx.doi.org/10.12688/f1000research.9207.1
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author Xie, Jianling
Wang, Xuemin
Proud, Christopher G.
author_facet Xie, Jianling
Wang, Xuemin
Proud, Christopher G.
author_sort Xie, Jianling
collection PubMed
description 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.
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spelling pubmed-50077572016-09-14 mTOR inhibitors in cancer therapy Xie, Jianling Wang, Xuemin Proud, Christopher G. F1000Res Review 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. F1000Research 2016-08-25 /pmc/articles/PMC5007757/ /pubmed/27635236 http://dx.doi.org/10.12688/f1000research.9207.1 Text en Copyright: © 2016 Xie J et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Xie, Jianling
Wang, Xuemin
Proud, Christopher G.
mTOR inhibitors in cancer therapy
title mTOR inhibitors in cancer therapy
title_full mTOR inhibitors in cancer therapy
title_fullStr mTOR inhibitors in cancer therapy
title_full_unstemmed mTOR inhibitors in cancer therapy
title_short mTOR inhibitors in cancer therapy
title_sort mtor inhibitors in cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5007757/
https://www.ncbi.nlm.nih.gov/pubmed/27635236
http://dx.doi.org/10.12688/f1000research.9207.1
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