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Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics

Delineating the contributions of specific cell signalling cascades to the development and maintenance of tumours has greatly informed our understanding of tumorigenesis and has advanced the modern era of targeted cancer therapy. It has been revealed that one of the key pathways regulating cell growt...

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Detalles Bibliográficos
Autores principales: Bhaoighill, Muireann Ní, Dunlop, Elaine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: OAE Publishing Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019212/
https://www.ncbi.nlm.nih.gov/pubmed/35582282
http://dx.doi.org/10.20517/cdr.2019.87
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author Bhaoighill, Muireann Ní
Dunlop, Elaine A.
author_facet Bhaoighill, Muireann Ní
Dunlop, Elaine A.
author_sort Bhaoighill, Muireann Ní
collection PubMed
description Delineating the contributions of specific cell signalling cascades to the development and maintenance of tumours has greatly informed our understanding of tumorigenesis and has advanced the modern era of targeted cancer therapy. It has been revealed that one of the key pathways regulating cell growth, the phosphatidylinositol 3-kinase/mechanistic target of rapamycin (PI3K/mTOR) signalling axis, is commonly dysregulated in cancer. With a specific, well-tolerated inhibitor of mTOR available, the impact of inhibiting this pathway at the level of mTOR has been tested clinically. This review highlights some of the promising results seen with mTOR inhibitors in the clinic and assesses some of the challenges that remain in predicting patient outcome following mTOR-targeted therapy.
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spelling pubmed-90192122022-05-16 Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics Bhaoighill, Muireann Ní Dunlop, Elaine A. Cancer Drug Resist Review Delineating the contributions of specific cell signalling cascades to the development and maintenance of tumours has greatly informed our understanding of tumorigenesis and has advanced the modern era of targeted cancer therapy. It has been revealed that one of the key pathways regulating cell growth, the phosphatidylinositol 3-kinase/mechanistic target of rapamycin (PI3K/mTOR) signalling axis, is commonly dysregulated in cancer. With a specific, well-tolerated inhibitor of mTOR available, the impact of inhibiting this pathway at the level of mTOR has been tested clinically. This review highlights some of the promising results seen with mTOR inhibitors in the clinic and assesses some of the challenges that remain in predicting patient outcome following mTOR-targeted therapy. OAE Publishing Inc. 2019-12-19 /pmc/articles/PMC9019212/ /pubmed/35582282 http://dx.doi.org/10.20517/cdr.2019.87 Text en © The Author(s) 2019. https://creativecommons.org/licenses/by/4.0/© The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Bhaoighill, Muireann Ní
Dunlop, Elaine A.
Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
title Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
title_full Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
title_fullStr Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
title_full_unstemmed Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
title_short Mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
title_sort mechanistic target of rapamycin inhibitors: successes and challenges as cancer therapeutics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019212/
https://www.ncbi.nlm.nih.gov/pubmed/35582282
http://dx.doi.org/10.20517/cdr.2019.87
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