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Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis

The biologic function of the CC chemokine macrophage inflammatory protein-1α (MIP-1α/CCL3) has been extensively studied since its initial identification as a macrophage-derived inflammatory mediator. In addition to its proinflammatory activities, CCL3 negatively regulates the proliferation of hemato...

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Detalles Bibliográficos
Autores principales: Baba, Tomohisa, Mukaida, Naofumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905173/
https://www.ncbi.nlm.nih.gov/pubmed/27308309
http://dx.doi.org/10.4161/mco.29899
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author Baba, Tomohisa
Mukaida, Naofumi
author_facet Baba, Tomohisa
Mukaida, Naofumi
author_sort Baba, Tomohisa
collection PubMed
description The biologic function of the CC chemokine macrophage inflammatory protein-1α (MIP-1α/CCL3) has been extensively studied since its initial identification as a macrophage-derived inflammatory mediator. In addition to its proinflammatory activities, CCL3 negatively regulates the proliferation of hematopoietic stem/progenitor cells (HSPCs). On the basis of this unique function, CCL3 is alternatively referred to as a stem cell inhibitor. This property has prompted many researchers to investigate the effects of CCL3 on normal physiologic hematopoiesis and pathophysiologic processes of hematopoietic malignancies. Consequently, there is accumulating evidence supporting a crucial involvement of CCL3 in the pathophysiology of several types of leukemia arising from neoplastic transformation of HSPCs. In this review we discuss the roles of CCL3 in leukemogenesis and its potential value as a target in a novel therapeutic strategy for the treatment of leukemia.
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spelling pubmed-49051732016-06-15 Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis Baba, Tomohisa Mukaida, Naofumi Mol Cell Oncol Review The biologic function of the CC chemokine macrophage inflammatory protein-1α (MIP-1α/CCL3) has been extensively studied since its initial identification as a macrophage-derived inflammatory mediator. In addition to its proinflammatory activities, CCL3 negatively regulates the proliferation of hematopoietic stem/progenitor cells (HSPCs). On the basis of this unique function, CCL3 is alternatively referred to as a stem cell inhibitor. This property has prompted many researchers to investigate the effects of CCL3 on normal physiologic hematopoiesis and pathophysiologic processes of hematopoietic malignancies. Consequently, there is accumulating evidence supporting a crucial involvement of CCL3 in the pathophysiology of several types of leukemia arising from neoplastic transformation of HSPCs. In this review we discuss the roles of CCL3 in leukemogenesis and its potential value as a target in a novel therapeutic strategy for the treatment of leukemia. Taylor & Francis 2014-07-15 /pmc/articles/PMC4905173/ /pubmed/27308309 http://dx.doi.org/10.4161/mco.29899 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
Baba, Tomohisa
Mukaida, Naofumi
Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis
title Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis
title_full Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis
title_fullStr Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis
title_full_unstemmed Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis
title_short Role of macrophage inflammatory protein (MIP)-1α/CCL3 in leukemogenesis
title_sort role of macrophage inflammatory protein (mip)-1α/ccl3 in leukemogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4905173/
https://www.ncbi.nlm.nih.gov/pubmed/27308309
http://dx.doi.org/10.4161/mco.29899
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