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Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies

In the last decade, the advent of biological targeted therapies has revolutionized the management of several types of cancer, especially in the realm of hematologic malignancies. One of these pathways, and the center of this review, is the phosphatidylinositol-3-kinase (PI3K) pathway. The PI3K pathw...

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Autores principales: Castillo, Jorge J, Iyengar, Meera, Kuritzky, Benjamin, Bishop, Kenneth D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937185/
https://www.ncbi.nlm.nih.gov/pubmed/24591840
http://dx.doi.org/10.2147/OTT.S34641
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author Castillo, Jorge J
Iyengar, Meera
Kuritzky, Benjamin
Bishop, Kenneth D
author_facet Castillo, Jorge J
Iyengar, Meera
Kuritzky, Benjamin
Bishop, Kenneth D
author_sort Castillo, Jorge J
collection PubMed
description In the last decade, the advent of biological targeted therapies has revolutionized the management of several types of cancer, especially in the realm of hematologic malignancies. One of these pathways, and the center of this review, is the phosphatidylinositol-3-kinase (PI3K) pathway. The PI3K pathway seems to play an important role in the pathogenesis and survival advantage in hematologic malignancies, such as leukemia, lymphoma, and myeloma. The objectives of the present review, hence, are to describe the current knowledge on the PI3K pathway and its isoforms, and to summarize preclinical and clinical studies using PI3K inhibitors, focusing on the advances made in hematologic malignancies.
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spelling pubmed-39371852014-03-03 Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies Castillo, Jorge J Iyengar, Meera Kuritzky, Benjamin Bishop, Kenneth D Onco Targets Ther Review In the last decade, the advent of biological targeted therapies has revolutionized the management of several types of cancer, especially in the realm of hematologic malignancies. One of these pathways, and the center of this review, is the phosphatidylinositol-3-kinase (PI3K) pathway. The PI3K pathway seems to play an important role in the pathogenesis and survival advantage in hematologic malignancies, such as leukemia, lymphoma, and myeloma. The objectives of the present review, hence, are to describe the current knowledge on the PI3K pathway and its isoforms, and to summarize preclinical and clinical studies using PI3K inhibitors, focusing on the advances made in hematologic malignancies. Dove Medical Press 2014-02-21 /pmc/articles/PMC3937185/ /pubmed/24591840 http://dx.doi.org/10.2147/OTT.S34641 Text en © 2014 Castillo et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Castillo, Jorge J
Iyengar, Meera
Kuritzky, Benjamin
Bishop, Kenneth D
Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
title Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
title_full Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
title_fullStr Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
title_full_unstemmed Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
title_short Isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
title_sort isotype-specific inhibition of the phosphatidylinositol-3-kinase pathway in hematologic malignancies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937185/
https://www.ncbi.nlm.nih.gov/pubmed/24591840
http://dx.doi.org/10.2147/OTT.S34641
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