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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2016
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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. |
format | Online Article Text |
id | pubmed-5007757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
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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