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Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy

Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, affecting approximately 21,000 people annually (nearly 11,000 deaths) in the United States. B-cell lymphoma 2 (BCL-2) family proteins, notably myeloid cell leukemia-1 (MCL-1), have been associated with both the develop...

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Autores principales: Kadia, Tapan Mahendra, Kantarjian, Hagop M., Konopleva, Marina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383813/
https://www.ncbi.nlm.nih.gov/pubmed/30815228
http://dx.doi.org/10.18632/oncotarget.26579
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author Kadia, Tapan Mahendra
Kantarjian, Hagop M.
Konopleva, Marina
author_facet Kadia, Tapan Mahendra
Kantarjian, Hagop M.
Konopleva, Marina
author_sort Kadia, Tapan Mahendra
collection PubMed
description Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, affecting approximately 21,000 people annually (nearly 11,000 deaths) in the United States. B-cell lymphoma 2 (BCL-2) family proteins, notably myeloid cell leukemia-1 (MCL-1), have been associated with both the development and persistence of AML. MCL-1 is one of the predominant BCL-2 family members expressed in samples from patients with untreated AML. MCL-1 is a critical cell survival factor for cancer and contributes to chemotherapy resistance by directly affecting cell death pathways. Here, we review the role of MCL-1 in AML and the mechanisms by which the potent cyclin-dependent kinase 9 inhibitor alvocidib, through regulation of MCL-1, may serve as a rational therapeutic approach against the disease.
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spelling pubmed-63838132019-02-27 Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy Kadia, Tapan Mahendra Kantarjian, Hagop M. Konopleva, Marina Oncotarget Review Acute myeloid leukemia (AML) is the most common form of acute leukemia in adults, affecting approximately 21,000 people annually (nearly 11,000 deaths) in the United States. B-cell lymphoma 2 (BCL-2) family proteins, notably myeloid cell leukemia-1 (MCL-1), have been associated with both the development and persistence of AML. MCL-1 is one of the predominant BCL-2 family members expressed in samples from patients with untreated AML. MCL-1 is a critical cell survival factor for cancer and contributes to chemotherapy resistance by directly affecting cell death pathways. Here, we review the role of MCL-1 in AML and the mechanisms by which the potent cyclin-dependent kinase 9 inhibitor alvocidib, through regulation of MCL-1, may serve as a rational therapeutic approach against the disease. Impact Journals LLC 2019-02-08 /pmc/articles/PMC6383813/ /pubmed/30815228 http://dx.doi.org/10.18632/oncotarget.26579 Text en Copyright: © 2019 Kadia et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Review
Kadia, Tapan Mahendra
Kantarjian, Hagop M.
Konopleva, Marina
Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
title Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
title_full Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
title_fullStr Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
title_full_unstemmed Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
title_short Myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
title_sort myeloid cell leukemia-1 dependence in acute myeloid leukemia: a novel approach to patient therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383813/
https://www.ncbi.nlm.nih.gov/pubmed/30815228
http://dx.doi.org/10.18632/oncotarget.26579
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