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PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer
The PI3K/AKT/mTOR (PAM) signaling pathway is a highly conserved signal transduction network in eukaryotic cells that promotes cell survival, cell growth, and cell cycle progression. Growth factor signalling to transcription factors in the PAM axis is highly regulated by multiple cross-interactions w...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436543/ https://www.ncbi.nlm.nih.gov/pubmed/37596643 http://dx.doi.org/10.1186/s12943-023-01827-6 |
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author | Glaviano, Antonino Foo, Aaron S. C. Lam, Hiu Y. Yap, Kenneth C. H. Jacot, William Jones, Robert H. Eng, Huiyan Nair, Madhumathy G. Makvandi, Pooyan Geoerger, Birgit Kulke, Matthew H. Baird, Richard D. Prabhu, Jyothi S. Carbone, Daniela Pecoraro, Camilla Teh, Daniel B. L. Sethi, Gautam Cavalieri, Vincenzo Lin, Kevin H. Javidi-Sharifi, Nathalie R. Toska, Eneda Davids, Matthew S. Brown, Jennifer R. Diana, Patrizia Stebbing, Justin Fruman, David A. Kumar, Alan P. |
author_facet | Glaviano, Antonino Foo, Aaron S. C. Lam, Hiu Y. Yap, Kenneth C. H. Jacot, William Jones, Robert H. Eng, Huiyan Nair, Madhumathy G. Makvandi, Pooyan Geoerger, Birgit Kulke, Matthew H. Baird, Richard D. Prabhu, Jyothi S. Carbone, Daniela Pecoraro, Camilla Teh, Daniel B. L. Sethi, Gautam Cavalieri, Vincenzo Lin, Kevin H. Javidi-Sharifi, Nathalie R. Toska, Eneda Davids, Matthew S. Brown, Jennifer R. Diana, Patrizia Stebbing, Justin Fruman, David A. Kumar, Alan P. |
author_sort | Glaviano, Antonino |
collection | PubMed |
description | The PI3K/AKT/mTOR (PAM) signaling pathway is a highly conserved signal transduction network in eukaryotic cells that promotes cell survival, cell growth, and cell cycle progression. Growth factor signalling to transcription factors in the PAM axis is highly regulated by multiple cross-interactions with several other signaling pathways, and dysregulation of signal transduction can predispose to cancer development. The PAM axis is the most frequently activated signaling pathway in human cancer and is often implicated in resistance to anticancer therapies. Dysfunction of components of this pathway such as hyperactivity of PI3K, loss of function of PTEN, and gain-of-function of AKT, are notorious drivers of treatment resistance and disease progression in cancer. In this review we highlight the major dysregulations in the PAM signaling pathway in cancer, and discuss the results of PI3K, AKT and mTOR inhibitors as monotherapy and in co-administation with other antineoplastic agents in clinical trials as a strategy for overcoming treatment resistance. Finally, the major mechanisms of resistance to PAM signaling targeted therapies, including PAM signaling in immunology and immunotherapies are also discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-023-01827-6. |
format | Online Article Text |
id | pubmed-10436543 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-104365432023-08-19 PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer Glaviano, Antonino Foo, Aaron S. C. Lam, Hiu Y. Yap, Kenneth C. H. Jacot, William Jones, Robert H. Eng, Huiyan Nair, Madhumathy G. Makvandi, Pooyan Geoerger, Birgit Kulke, Matthew H. Baird, Richard D. Prabhu, Jyothi S. Carbone, Daniela Pecoraro, Camilla Teh, Daniel B. L. Sethi, Gautam Cavalieri, Vincenzo Lin, Kevin H. Javidi-Sharifi, Nathalie R. Toska, Eneda Davids, Matthew S. Brown, Jennifer R. Diana, Patrizia Stebbing, Justin Fruman, David A. Kumar, Alan P. Mol Cancer Review The PI3K/AKT/mTOR (PAM) signaling pathway is a highly conserved signal transduction network in eukaryotic cells that promotes cell survival, cell growth, and cell cycle progression. Growth factor signalling to transcription factors in the PAM axis is highly regulated by multiple cross-interactions with several other signaling pathways, and dysregulation of signal transduction can predispose to cancer development. The PAM axis is the most frequently activated signaling pathway in human cancer and is often implicated in resistance to anticancer therapies. Dysfunction of components of this pathway such as hyperactivity of PI3K, loss of function of PTEN, and gain-of-function of AKT, are notorious drivers of treatment resistance and disease progression in cancer. In this review we highlight the major dysregulations in the PAM signaling pathway in cancer, and discuss the results of PI3K, AKT and mTOR inhibitors as monotherapy and in co-administation with other antineoplastic agents in clinical trials as a strategy for overcoming treatment resistance. Finally, the major mechanisms of resistance to PAM signaling targeted therapies, including PAM signaling in immunology and immunotherapies are also discussed. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12943-023-01827-6. BioMed Central 2023-08-18 /pmc/articles/PMC10436543/ /pubmed/37596643 http://dx.doi.org/10.1186/s12943-023-01827-6 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Glaviano, Antonino Foo, Aaron S. C. Lam, Hiu Y. Yap, Kenneth C. H. Jacot, William Jones, Robert H. Eng, Huiyan Nair, Madhumathy G. Makvandi, Pooyan Geoerger, Birgit Kulke, Matthew H. Baird, Richard D. Prabhu, Jyothi S. Carbone, Daniela Pecoraro, Camilla Teh, Daniel B. L. Sethi, Gautam Cavalieri, Vincenzo Lin, Kevin H. Javidi-Sharifi, Nathalie R. Toska, Eneda Davids, Matthew S. Brown, Jennifer R. Diana, Patrizia Stebbing, Justin Fruman, David A. Kumar, Alan P. PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer |
title | PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer |
title_full | PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer |
title_fullStr | PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer |
title_full_unstemmed | PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer |
title_short | PI3K/AKT/mTOR signaling transduction pathway and targeted therapies in cancer |
title_sort | pi3k/akt/mtor signaling transduction pathway and targeted therapies in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10436543/ https://www.ncbi.nlm.nih.gov/pubmed/37596643 http://dx.doi.org/10.1186/s12943-023-01827-6 |
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