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Macrophages as Key Drivers of Cancer Progression and Metastasis

Macrophages are one of the most abundant immune cells in the tumour microenvironment of solid tumours and their presence correlates with reduced survival in most cancers. Macrophages are present at all stages of tumour progression and stimulate angiogenesis, tumour cell invasion, and intravasation a...

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Autores principales: Nielsen, Sebastian R., Schmid, Michael C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292164/
https://www.ncbi.nlm.nih.gov/pubmed/28210073
http://dx.doi.org/10.1155/2017/9624760
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author Nielsen, Sebastian R.
Schmid, Michael C.
author_facet Nielsen, Sebastian R.
Schmid, Michael C.
author_sort Nielsen, Sebastian R.
collection PubMed
description Macrophages are one of the most abundant immune cells in the tumour microenvironment of solid tumours and their presence correlates with reduced survival in most cancers. Macrophages are present at all stages of tumour progression and stimulate angiogenesis, tumour cell invasion, and intravasation at the primary site. At the metastatic site, macrophages and monocytes prepare for the arrival of disseminated tumour cells and promote their extravasation and survival by inhibiting immune-mediated clearance or by directly engaging with tumour cells to activate prosurvival signalling pathways. In addition, macrophages promote the growth of disseminated tumour cells at the metastatic site by organising the formation of a supportive metastatic niche. The development of agents inhibiting the recruitment or the protumorigenic effector functions of macrophages in both the primary tumour and at the metastatic site is a promising strategy to improve cancer survival in the future.
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spelling pubmed-52921642017-02-16 Macrophages as Key Drivers of Cancer Progression and Metastasis Nielsen, Sebastian R. Schmid, Michael C. Mediators Inflamm Review Article Macrophages are one of the most abundant immune cells in the tumour microenvironment of solid tumours and their presence correlates with reduced survival in most cancers. Macrophages are present at all stages of tumour progression and stimulate angiogenesis, tumour cell invasion, and intravasation at the primary site. At the metastatic site, macrophages and monocytes prepare for the arrival of disseminated tumour cells and promote their extravasation and survival by inhibiting immune-mediated clearance or by directly engaging with tumour cells to activate prosurvival signalling pathways. In addition, macrophages promote the growth of disseminated tumour cells at the metastatic site by organising the formation of a supportive metastatic niche. The development of agents inhibiting the recruitment or the protumorigenic effector functions of macrophages in both the primary tumour and at the metastatic site is a promising strategy to improve cancer survival in the future. Hindawi Publishing Corporation 2017 2017-01-22 /pmc/articles/PMC5292164/ /pubmed/28210073 http://dx.doi.org/10.1155/2017/9624760 Text en Copyright © 2017 S. R. Nielsen and M. C. Schmid. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Nielsen, Sebastian R.
Schmid, Michael C.
Macrophages as Key Drivers of Cancer Progression and Metastasis
title Macrophages as Key Drivers of Cancer Progression and Metastasis
title_full Macrophages as Key Drivers of Cancer Progression and Metastasis
title_fullStr Macrophages as Key Drivers of Cancer Progression and Metastasis
title_full_unstemmed Macrophages as Key Drivers of Cancer Progression and Metastasis
title_short Macrophages as Key Drivers of Cancer Progression and Metastasis
title_sort macrophages as key drivers of cancer progression and metastasis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292164/
https://www.ncbi.nlm.nih.gov/pubmed/28210073
http://dx.doi.org/10.1155/2017/9624760
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