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Targeting PI3K in Cancer: Any Good News?
The phosphatidylinositol 3-kinase (PI3K) signaling pathway regulates several cellular processes and it’s one of the most frequently deregulated pathway in human tumors. Given its prominent role in cancer, there is great interest in the development of inhibitors able to target several members of PI3K...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647219/ https://www.ncbi.nlm.nih.gov/pubmed/23658859 http://dx.doi.org/10.3389/fonc.2013.00108 |
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author | Martini, Miriam Ciraolo, Elisa Gulluni, Federico Hirsch, Emilio |
author_facet | Martini, Miriam Ciraolo, Elisa Gulluni, Federico Hirsch, Emilio |
author_sort | Martini, Miriam |
collection | PubMed |
description | The phosphatidylinositol 3-kinase (PI3K) signaling pathway regulates several cellular processes and it’s one of the most frequently deregulated pathway in human tumors. Given its prominent role in cancer, there is great interest in the development of inhibitors able to target several members of PI3K signaling pathway in clinical trials. These drug candidates include PI3K inhibitors, both pan- and isoform-specific inhibitors, AKT, mTOR, and dual PI3K/mTOR inhibitors. As novel compounds progress into clinical trials, it’s becoming urgent to identify and select patient population that most likely benefit from PI3K inhibition. In this review we will discuss individual PIK3CA mutations as predictors of sensitivity and resistance to targeted therapies, leading to use of novel PI3K/mTOR/AKT inhibitors to a more “personalized” treatment. |
format | Online Article Text |
id | pubmed-3647219 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-36472192013-05-08 Targeting PI3K in Cancer: Any Good News? Martini, Miriam Ciraolo, Elisa Gulluni, Federico Hirsch, Emilio Front Oncol Oncology The phosphatidylinositol 3-kinase (PI3K) signaling pathway regulates several cellular processes and it’s one of the most frequently deregulated pathway in human tumors. Given its prominent role in cancer, there is great interest in the development of inhibitors able to target several members of PI3K signaling pathway in clinical trials. These drug candidates include PI3K inhibitors, both pan- and isoform-specific inhibitors, AKT, mTOR, and dual PI3K/mTOR inhibitors. As novel compounds progress into clinical trials, it’s becoming urgent to identify and select patient population that most likely benefit from PI3K inhibition. In this review we will discuss individual PIK3CA mutations as predictors of sensitivity and resistance to targeted therapies, leading to use of novel PI3K/mTOR/AKT inhibitors to a more “personalized” treatment. Frontiers Media S.A. 2013-05-08 /pmc/articles/PMC3647219/ /pubmed/23658859 http://dx.doi.org/10.3389/fonc.2013.00108 Text en Copyright © 2013 Martini, Ciraolo, Gulluni and Hirsch. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Oncology Martini, Miriam Ciraolo, Elisa Gulluni, Federico Hirsch, Emilio Targeting PI3K in Cancer: Any Good News? |
title | Targeting PI3K in Cancer: Any Good News? |
title_full | Targeting PI3K in Cancer: Any Good News? |
title_fullStr | Targeting PI3K in Cancer: Any Good News? |
title_full_unstemmed | Targeting PI3K in Cancer: Any Good News? |
title_short | Targeting PI3K in Cancer: Any Good News? |
title_sort | targeting pi3k in cancer: any good news? |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647219/ https://www.ncbi.nlm.nih.gov/pubmed/23658859 http://dx.doi.org/10.3389/fonc.2013.00108 |
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