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mTOR pathway: A current, up-to-date mini-review (Review)

Mammalian target of rapamycin (mTOR) is a protein serine/threonine kinase that was initially identified as the cellular target of rapamycin. This kinase regulates cell growth, proliferation, motility and survival, as well as the gene transcription and protein synthesis that are activated in response...

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Autores principales: ZAROGOULIDIS, PAUL, LAMPAKI, SOFIA, TURNER, J. FRANCIS, HUANG, HAIDONG, KAKOLYRIS, STYLIANOS, SYRIGOS, KONSTANTINOS, ZAROGOULIDIS, KONSTANTINOS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214394/
https://www.ncbi.nlm.nih.gov/pubmed/25360163
http://dx.doi.org/10.3892/ol.2014.2608
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author ZAROGOULIDIS, PAUL
LAMPAKI, SOFIA
TURNER, J. FRANCIS
HUANG, HAIDONG
KAKOLYRIS, STYLIANOS
SYRIGOS, KONSTANTINOS
ZAROGOULIDIS, KONSTANTINOS
author_facet ZAROGOULIDIS, PAUL
LAMPAKI, SOFIA
TURNER, J. FRANCIS
HUANG, HAIDONG
KAKOLYRIS, STYLIANOS
SYRIGOS, KONSTANTINOS
ZAROGOULIDIS, KONSTANTINOS
author_sort ZAROGOULIDIS, PAUL
collection PubMed
description Mammalian target of rapamycin (mTOR) is a protein serine/threonine kinase that was initially identified as the cellular target of rapamycin. This kinase regulates cell growth, proliferation, motility and survival, as well as the gene transcription and protein synthesis that are activated in response to hormones, growth factors and nutrients. Results from preclinical studies have indicated that factors antagonizing the mTOR pathway exert an antitumor effect on lung cancer. Furthermore, primary clinical trials of mTOR inhibitors have demonstrated that the inhibitors may be effective against lung carcinoma. The present study explores the association between mTOR and lung carcinogenesis and describes the clinical trials of mTOR inhibitors.
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spelling pubmed-42143942014-10-30 mTOR pathway: A current, up-to-date mini-review (Review) ZAROGOULIDIS, PAUL LAMPAKI, SOFIA TURNER, J. FRANCIS HUANG, HAIDONG KAKOLYRIS, STYLIANOS SYRIGOS, KONSTANTINOS ZAROGOULIDIS, KONSTANTINOS Oncol Lett Articles Mammalian target of rapamycin (mTOR) is a protein serine/threonine kinase that was initially identified as the cellular target of rapamycin. This kinase regulates cell growth, proliferation, motility and survival, as well as the gene transcription and protein synthesis that are activated in response to hormones, growth factors and nutrients. Results from preclinical studies have indicated that factors antagonizing the mTOR pathway exert an antitumor effect on lung cancer. Furthermore, primary clinical trials of mTOR inhibitors have demonstrated that the inhibitors may be effective against lung carcinoma. The present study explores the association between mTOR and lung carcinogenesis and describes the clinical trials of mTOR inhibitors. D.A. Spandidos 2014-12 2014-10-10 /pmc/articles/PMC4214394/ /pubmed/25360163 http://dx.doi.org/10.3892/ol.2014.2608 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
ZAROGOULIDIS, PAUL
LAMPAKI, SOFIA
TURNER, J. FRANCIS
HUANG, HAIDONG
KAKOLYRIS, STYLIANOS
SYRIGOS, KONSTANTINOS
ZAROGOULIDIS, KONSTANTINOS
mTOR pathway: A current, up-to-date mini-review (Review)
title mTOR pathway: A current, up-to-date mini-review (Review)
title_full mTOR pathway: A current, up-to-date mini-review (Review)
title_fullStr mTOR pathway: A current, up-to-date mini-review (Review)
title_full_unstemmed mTOR pathway: A current, up-to-date mini-review (Review)
title_short mTOR pathway: A current, up-to-date mini-review (Review)
title_sort mtor pathway: a current, up-to-date mini-review (review)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214394/
https://www.ncbi.nlm.nih.gov/pubmed/25360163
http://dx.doi.org/10.3892/ol.2014.2608
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