Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246

p53 gain of function mutants (mutp53) are involved in the pathogenesis of most human cancers. Here, the authors show that mutp53 regulates the tumor microenvironment by inducing the release of specific exosomes containing miR-1246 that once received by macrophages turns them into tumor supportive ma...

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Main Authors: Tomer Cooks, Ioannis S. Pateras, Lisa M. Jenkins, Keval M. Patel, Ana I. Robles, James Morris, Tim Forshew, Ettore Appella, Vassilis G. Gorgoulis, Curtis C. Harris
Format: Article
Language:English
Published: Nature Portfolio 2018-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-018-03224-w
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author Tomer Cooks
Ioannis S. Pateras
Lisa M. Jenkins
Keval M. Patel
Ana I. Robles
James Morris
Tim Forshew
Ettore Appella
Vassilis G. Gorgoulis
Curtis C. Harris
author_facet Tomer Cooks
Ioannis S. Pateras
Lisa M. Jenkins
Keval M. Patel
Ana I. Robles
James Morris
Tim Forshew
Ettore Appella
Vassilis G. Gorgoulis
Curtis C. Harris
author_sort Tomer Cooks
collection DOAJ
description p53 gain of function mutants (mutp53) are involved in the pathogenesis of most human cancers. Here, the authors show that mutp53 regulates the tumor microenvironment by inducing the release of specific exosomes containing miR-1246 that once received by macrophages turns them into tumor supportive macrophages.
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spelling doaj.art-c7c38fedb00642b095bd023227041cc02022-12-21T18:32:04ZengNature PortfolioNature Communications2041-17232018-02-019111510.1038/s41467-018-03224-wMutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246Tomer Cooks0Ioannis S. Pateras1Lisa M. Jenkins2Keval M. Patel3Ana I. Robles4James Morris5Tim Forshew6Ettore Appella7Vassilis G. Gorgoulis8Curtis C. Harris9Laboratory of Human Carcinogenesis, NCI-CCR, National Institutes of HealthMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, National Kapodistrian University of AthensLaboratory of Cell Biology, National Cancer Institute, National Institutes of HealthAddenbrooke’s HospitalLaboratory of Human Carcinogenesis, NCI-CCR, National Institutes of HealthCancer Research UK, Cambridge Research InstituteUCL Cancer InstituteLaboratory of Cell Biology, National Cancer Institute, National Institutes of HealthMolecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, National Kapodistrian University of AthensLaboratory of Human Carcinogenesis, NCI-CCR, National Institutes of Healthp53 gain of function mutants (mutp53) are involved in the pathogenesis of most human cancers. Here, the authors show that mutp53 regulates the tumor microenvironment by inducing the release of specific exosomes containing miR-1246 that once received by macrophages turns them into tumor supportive macrophages.https://doi.org/10.1038/s41467-018-03224-w
spellingShingle Tomer Cooks
Ioannis S. Pateras
Lisa M. Jenkins
Keval M. Patel
Ana I. Robles
James Morris
Tim Forshew
Ettore Appella
Vassilis G. Gorgoulis
Curtis C. Harris
Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
Nature Communications
title Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
title_full Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
title_fullStr Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
title_full_unstemmed Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
title_short Mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal miR-1246
title_sort mutant p53 cancers reprogram macrophages to tumor supporting macrophages via exosomal mir 1246
url https://doi.org/10.1038/s41467-018-03224-w
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