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A shortcut for early macrophage recruitment into tumors by activated oncogenes

Macrophages play an important role in tumor promotion, usually acting as facilitators of cancer initiation and progression. However, it is not clear how macrophages impact early phases of tumorigenesis. Using genetically modified mouse models, Guo et al. (pp. 247–259) demonstrated that tumor-initiat...

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Detalles Bibliográficos
Autores principales: Austenaa, Liv, Natoli, Gioacchino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358718/
https://www.ncbi.nlm.nih.gov/pubmed/28270513
http://dx.doi.org/10.1101/gad.296905.117
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author Austenaa, Liv
Natoli, Gioacchino
author_facet Austenaa, Liv
Natoli, Gioacchino
author_sort Austenaa, Liv
collection PubMed
description Macrophages play an important role in tumor promotion, usually acting as facilitators of cancer initiation and progression. However, it is not clear how macrophages impact early phases of tumorigenesis. Using genetically modified mouse models, Guo et al. (pp. 247–259) demonstrated that tumor-initiating cells with an activated Hippo pathway are able to recruit macrophages starting from the very early phases of cancer development, mainly through direct activation of genes encoding macrophage chemoattractants and survival factors. The recruited macrophages were of vital importance for protection of tumor-initiating cells against eradication by lymphocyte-mediated immune surveillance. Such a tight link between macrophages and a pathway controlling organ development and size may reflect the normal role of these cells in tissue morphogenesis.
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spelling pubmed-53587182017-08-01 A shortcut for early macrophage recruitment into tumors by activated oncogenes Austenaa, Liv Natoli, Gioacchino Genes Dev Outlook Macrophages play an important role in tumor promotion, usually acting as facilitators of cancer initiation and progression. However, it is not clear how macrophages impact early phases of tumorigenesis. Using genetically modified mouse models, Guo et al. (pp. 247–259) demonstrated that tumor-initiating cells with an activated Hippo pathway are able to recruit macrophages starting from the very early phases of cancer development, mainly through direct activation of genes encoding macrophage chemoattractants and survival factors. The recruited macrophages were of vital importance for protection of tumor-initiating cells against eradication by lymphocyte-mediated immune surveillance. Such a tight link between macrophages and a pathway controlling organ development and size may reflect the normal role of these cells in tissue morphogenesis. Cold Spring Harbor Laboratory Press 2017-02-01 /pmc/articles/PMC5358718/ /pubmed/28270513 http://dx.doi.org/10.1101/gad.296905.117 Text en © 2017 Austenaa and Natoli; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Outlook
Austenaa, Liv
Natoli, Gioacchino
A shortcut for early macrophage recruitment into tumors by activated oncogenes
title A shortcut for early macrophage recruitment into tumors by activated oncogenes
title_full A shortcut for early macrophage recruitment into tumors by activated oncogenes
title_fullStr A shortcut for early macrophage recruitment into tumors by activated oncogenes
title_full_unstemmed A shortcut for early macrophage recruitment into tumors by activated oncogenes
title_short A shortcut for early macrophage recruitment into tumors by activated oncogenes
title_sort shortcut for early macrophage recruitment into tumors by activated oncogenes
topic Outlook
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5358718/
https://www.ncbi.nlm.nih.gov/pubmed/28270513
http://dx.doi.org/10.1101/gad.296905.117
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