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Bone marrow niches in myeloid neoplasms

Pathological phenotypes of myeloid neoplasms are closely related to genetic/chromosomal abnormalities of neoplastic cells whereas the bone marrow microenvironment, including stromal elements and hematopoietic stem cell niche cells, have a great influence on the differentiation/proliferation of both...

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Autores principales: Kitagawa, Masanobu, Kurata, Morito, Onishi, Iichiroh, Yamamoto, Kouhei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232432/
https://www.ncbi.nlm.nih.gov/pubmed/31709722
http://dx.doi.org/10.1111/pin.12870
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author Kitagawa, Masanobu
Kurata, Morito
Onishi, Iichiroh
Yamamoto, Kouhei
author_facet Kitagawa, Masanobu
Kurata, Morito
Onishi, Iichiroh
Yamamoto, Kouhei
author_sort Kitagawa, Masanobu
collection PubMed
description Pathological phenotypes of myeloid neoplasms are closely related to genetic/chromosomal abnormalities of neoplastic cells whereas the bone marrow microenvironment, including stromal elements and hematopoietic stem cell niche cells, have a great influence on the differentiation/proliferation of both hematopoietic and neoplastic cells. The pathology of myeloid neoplasms might be generated through the interaction of hematopoietic (stem) cells and stromal cells. The present study aims to provide the morphological/functional aspects of the bone marrow environment in myeloid neoplasms. Among the myeloid neoplasms, myelodysplastic syndromes (MDS) exhibit significant and complex interactions between neoplastic cells and stromal cells. Hematopoietic cells in MDS are greatly influenced by macrophages/niche cells via several signaling pathways. As such, the pathological significance of cell proliferation, cell apoptosis, and anti‐apoptosis signals in the bone marrow of myeloid neoplasms, especially MDS bone marrow, will be discussed.
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spelling pubmed-72324322020-05-19 Bone marrow niches in myeloid neoplasms Kitagawa, Masanobu Kurata, Morito Onishi, Iichiroh Yamamoto, Kouhei Pathol Int Review Article Pathological phenotypes of myeloid neoplasms are closely related to genetic/chromosomal abnormalities of neoplastic cells whereas the bone marrow microenvironment, including stromal elements and hematopoietic stem cell niche cells, have a great influence on the differentiation/proliferation of both hematopoietic and neoplastic cells. The pathology of myeloid neoplasms might be generated through the interaction of hematopoietic (stem) cells and stromal cells. The present study aims to provide the morphological/functional aspects of the bone marrow environment in myeloid neoplasms. Among the myeloid neoplasms, myelodysplastic syndromes (MDS) exhibit significant and complex interactions between neoplastic cells and stromal cells. Hematopoietic cells in MDS are greatly influenced by macrophages/niche cells via several signaling pathways. As such, the pathological significance of cell proliferation, cell apoptosis, and anti‐apoptosis signals in the bone marrow of myeloid neoplasms, especially MDS bone marrow, will be discussed. John Wiley and Sons Inc. 2019-11-10 2020-02 /pmc/articles/PMC7232432/ /pubmed/31709722 http://dx.doi.org/10.1111/pin.12870 Text en © 2019 The Authors. Pathology International published by Japanese Society of Pathology and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kitagawa, Masanobu
Kurata, Morito
Onishi, Iichiroh
Yamamoto, Kouhei
Bone marrow niches in myeloid neoplasms
title Bone marrow niches in myeloid neoplasms
title_full Bone marrow niches in myeloid neoplasms
title_fullStr Bone marrow niches in myeloid neoplasms
title_full_unstemmed Bone marrow niches in myeloid neoplasms
title_short Bone marrow niches in myeloid neoplasms
title_sort bone marrow niches in myeloid neoplasms
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232432/
https://www.ncbi.nlm.nih.gov/pubmed/31709722
http://dx.doi.org/10.1111/pin.12870
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