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mTOR and Tumor Cachexia
Cancer cachexia affects most patients with advanced forms of cancers. It is mainly characterized by weight loss, due to muscle and adipose mass depletion. As cachexia is associated with increased morbidity and mortality in cancer patients, identifying the underlying mechanisms leading to cachexia is...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121479/ https://www.ncbi.nlm.nih.gov/pubmed/30061533 http://dx.doi.org/10.3390/ijms19082225 |
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author | Duval, Adrian P. Jeanneret, Cheryl Santoro, Tania Dormond, Olivier |
author_facet | Duval, Adrian P. Jeanneret, Cheryl Santoro, Tania Dormond, Olivier |
author_sort | Duval, Adrian P. |
collection | PubMed |
description | Cancer cachexia affects most patients with advanced forms of cancers. It is mainly characterized by weight loss, due to muscle and adipose mass depletion. As cachexia is associated with increased morbidity and mortality in cancer patients, identifying the underlying mechanisms leading to cachexia is essential in order to design novel therapeutic strategies. The mechanistic target of rapamycin (mTOR) is a major intracellular signalling intermediary that participates in cell growth by upregulating anabolic processes such as protein and lipid synthesis. Accordingly, emerging evidence suggests that mTOR and mTOR inhibitors influence cancer cachexia. Here, we review the role of mTOR in cellular processes involved in cancer cachexia and highlight the studies supporting the contribution of mTOR in cancer cachexia. |
format | Online Article Text |
id | pubmed-6121479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61214792018-09-07 mTOR and Tumor Cachexia Duval, Adrian P. Jeanneret, Cheryl Santoro, Tania Dormond, Olivier Int J Mol Sci Review Cancer cachexia affects most patients with advanced forms of cancers. It is mainly characterized by weight loss, due to muscle and adipose mass depletion. As cachexia is associated with increased morbidity and mortality in cancer patients, identifying the underlying mechanisms leading to cachexia is essential in order to design novel therapeutic strategies. The mechanistic target of rapamycin (mTOR) is a major intracellular signalling intermediary that participates in cell growth by upregulating anabolic processes such as protein and lipid synthesis. Accordingly, emerging evidence suggests that mTOR and mTOR inhibitors influence cancer cachexia. Here, we review the role of mTOR in cellular processes involved in cancer cachexia and highlight the studies supporting the contribution of mTOR in cancer cachexia. MDPI 2018-07-30 /pmc/articles/PMC6121479/ /pubmed/30061533 http://dx.doi.org/10.3390/ijms19082225 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Duval, Adrian P. Jeanneret, Cheryl Santoro, Tania Dormond, Olivier mTOR and Tumor Cachexia |
title | mTOR and Tumor Cachexia |
title_full | mTOR and Tumor Cachexia |
title_fullStr | mTOR and Tumor Cachexia |
title_full_unstemmed | mTOR and Tumor Cachexia |
title_short | mTOR and Tumor Cachexia |
title_sort | mtor and tumor cachexia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121479/ https://www.ncbi.nlm.nih.gov/pubmed/30061533 http://dx.doi.org/10.3390/ijms19082225 |
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