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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...

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Detalles Bibliográficos
Autores principales: Duval, Adrian P., Jeanneret, Cheryl, Santoro, Tania, Dormond, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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