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Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression
Despite the advent of many therapeutic agents, such as bortezomib and lenalidomide that have significantly improved the overall survival, multiple myeloma remains an incurable disease. Failure to cure is multifactorial and can be attributed to the underlying genetic heterogeneity of the cancer and t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386771/ https://www.ncbi.nlm.nih.gov/pubmed/28099912 http://dx.doi.org/10.18632/oncotarget.14610 |
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author | Mondello, Patrizia Cuzzocrea, Salvatore Navarra, Michele Mian, Michael |
author_facet | Mondello, Patrizia Cuzzocrea, Salvatore Navarra, Michele Mian, Michael |
author_sort | Mondello, Patrizia |
collection | PubMed |
description | Despite the advent of many therapeutic agents, such as bortezomib and lenalidomide that have significantly improved the overall survival, multiple myeloma remains an incurable disease. Failure to cure is multifactorial and can be attributed to the underlying genetic heterogeneity of the cancer and to the surrounding micro-environment. Understanding the mutual interaction between myeloma cells and micro-environment may lead to the development of novel treatment strategies able to eradicate this disease. In this review we discuss the principal molecules involved in the micro-environment network in multiple myeloma and the currently available therapies targeting them. |
format | Online Article Text |
id | pubmed-5386771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53867712017-04-26 Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression Mondello, Patrizia Cuzzocrea, Salvatore Navarra, Michele Mian, Michael Oncotarget Review Despite the advent of many therapeutic agents, such as bortezomib and lenalidomide that have significantly improved the overall survival, multiple myeloma remains an incurable disease. Failure to cure is multifactorial and can be attributed to the underlying genetic heterogeneity of the cancer and to the surrounding micro-environment. Understanding the mutual interaction between myeloma cells and micro-environment may lead to the development of novel treatment strategies able to eradicate this disease. In this review we discuss the principal molecules involved in the micro-environment network in multiple myeloma and the currently available therapies targeting them. Impact Journals LLC 2017-01-12 /pmc/articles/PMC5386771/ /pubmed/28099912 http://dx.doi.org/10.18632/oncotarget.14610 Text en Copyright: © 2017 Mondello et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Mondello, Patrizia Cuzzocrea, Salvatore Navarra, Michele Mian, Michael Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
title | Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
title_full | Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
title_fullStr | Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
title_full_unstemmed | Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
title_short | Bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
title_sort | bone marrow micro-environment is a crucial player for myelomagenesis and disease progression |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386771/ https://www.ncbi.nlm.nih.gov/pubmed/28099912 http://dx.doi.org/10.18632/oncotarget.14610 |
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