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Nanotechnology-Based Targeting of mTOR Signaling in Cancer

Mammalian target of rapamycin (mTOR) is a master regulator of cell growth and metabolism, which is activated in response to intra- and extracellular signals, including nutrients, growth factors, and cellular energy levels. The frequent dysregulation of mTOR signaling in cancer makes it an attractive...

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Autor principal: Yoon, Mee-Sup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418174/
https://www.ncbi.nlm.nih.gov/pubmed/32821100
http://dx.doi.org/10.2147/IJN.S254574
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author Yoon, Mee-Sup
author_facet Yoon, Mee-Sup
author_sort Yoon, Mee-Sup
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description Mammalian target of rapamycin (mTOR) is a master regulator of cell growth and metabolism, which is activated in response to intra- and extracellular signals, including nutrients, growth factors, and cellular energy levels. The frequent dysregulation of mTOR signaling in cancer makes it an attractive therapeutic target, and several types of mTOR inhibitors have been developed. Nanoparticle-based mTOR modulators are predicted to target various cancers and deliver as well as release drugs in a controlled manner, resulting in enhanced bioavailability and reduced side effects. This mini-review is focused on the molecular mechanism of nanoparticle-based mTOR modulator action as well as the current development of mTOR inhibitors using nanoparticles. Understanding the biological function of nanoparticle-based mTOR modulators will contribute to the development of efficient nano-therapeutics for the treatment of cancers.
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spelling pubmed-74181742020-08-19 Nanotechnology-Based Targeting of mTOR Signaling in Cancer Yoon, Mee-Sup Int J Nanomedicine Review Mammalian target of rapamycin (mTOR) is a master regulator of cell growth and metabolism, which is activated in response to intra- and extracellular signals, including nutrients, growth factors, and cellular energy levels. The frequent dysregulation of mTOR signaling in cancer makes it an attractive therapeutic target, and several types of mTOR inhibitors have been developed. Nanoparticle-based mTOR modulators are predicted to target various cancers and deliver as well as release drugs in a controlled manner, resulting in enhanced bioavailability and reduced side effects. This mini-review is focused on the molecular mechanism of nanoparticle-based mTOR modulator action as well as the current development of mTOR inhibitors using nanoparticles. Understanding the biological function of nanoparticle-based mTOR modulators will contribute to the development of efficient nano-therapeutics for the treatment of cancers. Dove 2020-08-06 /pmc/articles/PMC7418174/ /pubmed/32821100 http://dx.doi.org/10.2147/IJN.S254574 Text en © 2020 Yoon. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Review
Yoon, Mee-Sup
Nanotechnology-Based Targeting of mTOR Signaling in Cancer
title Nanotechnology-Based Targeting of mTOR Signaling in Cancer
title_full Nanotechnology-Based Targeting of mTOR Signaling in Cancer
title_fullStr Nanotechnology-Based Targeting of mTOR Signaling in Cancer
title_full_unstemmed Nanotechnology-Based Targeting of mTOR Signaling in Cancer
title_short Nanotechnology-Based Targeting of mTOR Signaling in Cancer
title_sort nanotechnology-based targeting of mtor signaling in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418174/
https://www.ncbi.nlm.nih.gov/pubmed/32821100
http://dx.doi.org/10.2147/IJN.S254574
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