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Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?

The activation of the PI3K/AKT/mTOR pathway is a main driver of cell growth, proliferation, survival, and chemoresistance of cancer cells, and, for this reason, represents an attractive target for developing targeted anti-cancer drugs. There are plenty of preclinical data sustaining the anti-tumor a...

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Autores principales: Tarantelli, Chiara, Lupia, Antonio, Stathis, Anastasios, Bertoni, Francesco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037719/
https://www.ncbi.nlm.nih.gov/pubmed/32033478
http://dx.doi.org/10.3390/ijms21031060
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author Tarantelli, Chiara
Lupia, Antonio
Stathis, Anastasios
Bertoni, Francesco
author_facet Tarantelli, Chiara
Lupia, Antonio
Stathis, Anastasios
Bertoni, Francesco
author_sort Tarantelli, Chiara
collection PubMed
description The activation of the PI3K/AKT/mTOR pathway is a main driver of cell growth, proliferation, survival, and chemoresistance of cancer cells, and, for this reason, represents an attractive target for developing targeted anti-cancer drugs. There are plenty of preclinical data sustaining the anti-tumor activity of dual PI3K/mTOR inhibitors as single agents and in combination in lymphomas. Clinical responses, including complete remissions (especially in follicular lymphoma patients), are also observed in the very few clinical studies performed in patients that are affected by relapsed/refractory lymphomas or chronic lymphocytic leukemia. In this review, we summarize the literature on dual PI3K/mTOR inhibitors focusing on the lymphoma setting, presenting both the three compounds still in clinical development and those with a clinical program stopped or put on hold.
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spelling pubmed-70377192020-03-10 Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma? Tarantelli, Chiara Lupia, Antonio Stathis, Anastasios Bertoni, Francesco Int J Mol Sci Review The activation of the PI3K/AKT/mTOR pathway is a main driver of cell growth, proliferation, survival, and chemoresistance of cancer cells, and, for this reason, represents an attractive target for developing targeted anti-cancer drugs. There are plenty of preclinical data sustaining the anti-tumor activity of dual PI3K/mTOR inhibitors as single agents and in combination in lymphomas. Clinical responses, including complete remissions (especially in follicular lymphoma patients), are also observed in the very few clinical studies performed in patients that are affected by relapsed/refractory lymphomas or chronic lymphocytic leukemia. In this review, we summarize the literature on dual PI3K/mTOR inhibitors focusing on the lymphoma setting, presenting both the three compounds still in clinical development and those with a clinical program stopped or put on hold. MDPI 2020-02-05 /pmc/articles/PMC7037719/ /pubmed/32033478 http://dx.doi.org/10.3390/ijms21031060 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tarantelli, Chiara
Lupia, Antonio
Stathis, Anastasios
Bertoni, Francesco
Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?
title Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?
title_full Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?
title_fullStr Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?
title_full_unstemmed Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?
title_short Is There a Role for Dual PI3K/mTOR Inhibitors for Patients Affected with Lymphoma?
title_sort is there a role for dual pi3k/mtor inhibitors for patients affected with lymphoma?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037719/
https://www.ncbi.nlm.nih.gov/pubmed/32033478
http://dx.doi.org/10.3390/ijms21031060
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