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TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors

Tumor necrosis factor (TNF) is widely accepted as a tumor-suppressive cytokine via its ubiquitous receptor TNF receptor 1 (TNFR1). The other receptor, TNFR2, is not only expressed on some tumor cells but also on suppressive immune cells, including regulatory T cells and myeloid-derived suppressor ce...

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Detalles Bibliográficos
Autores principales: Sheng, Yuqiao, Li, Feng, Qin, Zhihai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985372/
https://www.ncbi.nlm.nih.gov/pubmed/29892300
http://dx.doi.org/10.3389/fimmu.2018.01170
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author Sheng, Yuqiao
Li, Feng
Qin, Zhihai
author_facet Sheng, Yuqiao
Li, Feng
Qin, Zhihai
author_sort Sheng, Yuqiao
collection PubMed
description Tumor necrosis factor (TNF) is widely accepted as a tumor-suppressive cytokine via its ubiquitous receptor TNF receptor 1 (TNFR1). The other receptor, TNFR2, is not only expressed on some tumor cells but also on suppressive immune cells, including regulatory T cells and myeloid-derived suppressor cells. In contrast to TNFR1, TNFR2 diverts the tumor-inhibiting TNF into a tumor-advocating factor. TNFR2 directly promotes the proliferation of some kinds of tumor cells. Also activating immunosuppressive cells, it supports immune escape and tumor development. Hence, TNFR2 may represent a potential target of cancer therapy. Here, we focus on expression and role of TNFR2 in the tumor microenvironment. We summarize the recent progress in understanding how TNFR2-dependent mechanisms promote carcinogenesis and tumor growth and discuss the potential value of TNFR2 in cancer treatment.
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spelling pubmed-59853722018-06-11 TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors Sheng, Yuqiao Li, Feng Qin, Zhihai Front Immunol Immunology Tumor necrosis factor (TNF) is widely accepted as a tumor-suppressive cytokine via its ubiquitous receptor TNF receptor 1 (TNFR1). The other receptor, TNFR2, is not only expressed on some tumor cells but also on suppressive immune cells, including regulatory T cells and myeloid-derived suppressor cells. In contrast to TNFR1, TNFR2 diverts the tumor-inhibiting TNF into a tumor-advocating factor. TNFR2 directly promotes the proliferation of some kinds of tumor cells. Also activating immunosuppressive cells, it supports immune escape and tumor development. Hence, TNFR2 may represent a potential target of cancer therapy. Here, we focus on expression and role of TNFR2 in the tumor microenvironment. We summarize the recent progress in understanding how TNFR2-dependent mechanisms promote carcinogenesis and tumor growth and discuss the potential value of TNFR2 in cancer treatment. Frontiers Media S.A. 2018-05-28 /pmc/articles/PMC5985372/ /pubmed/29892300 http://dx.doi.org/10.3389/fimmu.2018.01170 Text en Copyright © 2018 Sheng, Li and Qin. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sheng, Yuqiao
Li, Feng
Qin, Zhihai
TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors
title TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors
title_full TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors
title_fullStr TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors
title_full_unstemmed TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors
title_short TNF Receptor 2 Makes Tumor Necrosis Factor a Friend of Tumors
title_sort tnf receptor 2 makes tumor necrosis factor a friend of tumors
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985372/
https://www.ncbi.nlm.nih.gov/pubmed/29892300
http://dx.doi.org/10.3389/fimmu.2018.01170
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