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Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?

Acquired resistance toward apoptosis represents one of the hallmarks of human cancer and a major cause of the inefficacy of most anticancer treatment regimens. Based on its ability to inhibit apoptosis, the B-cell lymphoma/leukemia 2 (Bcl-2) protein family has garnered the most attention as a promis...

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Detalles Bibliográficos
Autores principales: Brinkmann, K, Kashkar, H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973243/
https://www.ncbi.nlm.nih.gov/pubmed/24603326
http://dx.doi.org/10.1038/cddis.2014.61
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author Brinkmann, K
Kashkar, H
author_facet Brinkmann, K
Kashkar, H
author_sort Brinkmann, K
collection PubMed
description Acquired resistance toward apoptosis represents one of the hallmarks of human cancer and a major cause of the inefficacy of most anticancer treatment regimens. Based on its ability to inhibit apoptosis, the B-cell lymphoma/leukemia 2 (Bcl-2) protein family has garnered the most attention as a promising therapeutic target in cancer. Accordingly, efforts have lately been focused on the development of drugs targeting Bcl-2 proteins with considerable therapeutic success, particularly in hematologic malignancies. Here, we review the previous studies and highlight the pivotal role of the Bcl-2 protein family in the homeostasis of hematologic tissue compartment. This knowledge provides more insight into why some cancers are more sensitive to Bcl-2 targeting than others and will foster the clinical evaluation of Bcl-2-targeting strategies in cancer by avoiding severe on-target side effects in the development of healthy tissues.
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spelling pubmed-39732432014-04-02 Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies? Brinkmann, K Kashkar, H Cell Death Dis Review Acquired resistance toward apoptosis represents one of the hallmarks of human cancer and a major cause of the inefficacy of most anticancer treatment regimens. Based on its ability to inhibit apoptosis, the B-cell lymphoma/leukemia 2 (Bcl-2) protein family has garnered the most attention as a promising therapeutic target in cancer. Accordingly, efforts have lately been focused on the development of drugs targeting Bcl-2 proteins with considerable therapeutic success, particularly in hematologic malignancies. Here, we review the previous studies and highlight the pivotal role of the Bcl-2 protein family in the homeostasis of hematologic tissue compartment. This knowledge provides more insight into why some cancers are more sensitive to Bcl-2 targeting than others and will foster the clinical evaluation of Bcl-2-targeting strategies in cancer by avoiding severe on-target side effects in the development of healthy tissues. Nature Publishing Group 2014-03 2014-03-06 /pmc/articles/PMC3973243/ /pubmed/24603326 http://dx.doi.org/10.1038/cddis.2014.61 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Review
Brinkmann, K
Kashkar, H
Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
title Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
title_full Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
title_fullStr Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
title_full_unstemmed Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
title_short Targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
title_sort targeting the mitochondrial apoptotic pathway: a preferred approach in hematologic malignancies?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3973243/
https://www.ncbi.nlm.nih.gov/pubmed/24603326
http://dx.doi.org/10.1038/cddis.2014.61
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