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Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment

Targeting kinase activity is considered to be an attractive therapeutic strategy to overcome acute myeloid leukemia (AML) since aberrant activation of the kinase pathway plays a pivotal role in leukemogenesis through abnormal cell proliferation and differentiation block. Although clinical trials for...

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Autor principal: Takahashi, Shinichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297912/
https://www.ncbi.nlm.nih.gov/pubmed/37367084
http://dx.doi.org/10.3390/hematolrep15020035
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author Takahashi, Shinichiro
author_facet Takahashi, Shinichiro
author_sort Takahashi, Shinichiro
collection PubMed
description Targeting kinase activity is considered to be an attractive therapeutic strategy to overcome acute myeloid leukemia (AML) since aberrant activation of the kinase pathway plays a pivotal role in leukemogenesis through abnormal cell proliferation and differentiation block. Although clinical trials for kinase modulators as single agents remain scarce, combination therapies are an area of therapeutic interest. In this review, the author summarizes attractive kinase pathways for therapeutic targets and the combination strategies for these pathways. Specifically, the review focuses on combination therapies targeting the FLT3 pathways, as well as PI3K/AKT/mTOR, CDK and CHK1 pathways. From a literature review, combination therapies with the kinase inhibitors appear more promising than monotherapies with individual agents. Therefore, the development of efficient combination therapies with kinase inhibitors may result in effective therapeutic strategies for AML.
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spelling pubmed-102979122023-06-28 Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment Takahashi, Shinichiro Hematol Rep Review Targeting kinase activity is considered to be an attractive therapeutic strategy to overcome acute myeloid leukemia (AML) since aberrant activation of the kinase pathway plays a pivotal role in leukemogenesis through abnormal cell proliferation and differentiation block. Although clinical trials for kinase modulators as single agents remain scarce, combination therapies are an area of therapeutic interest. In this review, the author summarizes attractive kinase pathways for therapeutic targets and the combination strategies for these pathways. Specifically, the review focuses on combination therapies targeting the FLT3 pathways, as well as PI3K/AKT/mTOR, CDK and CHK1 pathways. From a literature review, combination therapies with the kinase inhibitors appear more promising than monotherapies with individual agents. Therefore, the development of efficient combination therapies with kinase inhibitors may result in effective therapeutic strategies for AML. MDPI 2023-05-24 /pmc/articles/PMC10297912/ /pubmed/37367084 http://dx.doi.org/10.3390/hematolrep15020035 Text en © 2023 by the author. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Takahashi, Shinichiro
Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment
title Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment
title_full Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment
title_fullStr Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment
title_full_unstemmed Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment
title_short Combination Therapies with Kinase Inhibitors for Acute Myeloid Leukemia Treatment
title_sort combination therapies with kinase inhibitors for acute myeloid leukemia treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297912/
https://www.ncbi.nlm.nih.gov/pubmed/37367084
http://dx.doi.org/10.3390/hematolrep15020035
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