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Escape from IFN-γ-dependent immunosurveillance in tumorigenesis
Immune interferon (IFN), also known as IFN-γ, promotes not only immunomodulation but also antimicrobial and anticancer activity. After IFN-γ binds to the complex of IFN-γ receptor (IFNGR) 1-IFNGR2 and subsequently activates its downstream signaling pathways, IFN-γ immediately causes transcriptional...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286687/ https://www.ncbi.nlm.nih.gov/pubmed/28143527 http://dx.doi.org/10.1186/s12929-017-0317-0 |
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author | Lin, Chiou-Feng Lin, Chih-Ming Lee, Kang-Yun Wu, Szu-Yuan Feng, Po-Hao Chen, Kuan-Yuan Chuang, Hsiao-Chi Chen, Chia-Ling Wang, Yu-Chih Tseng, Po-Chun Tsai, Tsung-Ting |
author_facet | Lin, Chiou-Feng Lin, Chih-Ming Lee, Kang-Yun Wu, Szu-Yuan Feng, Po-Hao Chen, Kuan-Yuan Chuang, Hsiao-Chi Chen, Chia-Ling Wang, Yu-Chih Tseng, Po-Chun Tsai, Tsung-Ting |
author_sort | Lin, Chiou-Feng |
collection | PubMed |
description | Immune interferon (IFN), also known as IFN-γ, promotes not only immunomodulation but also antimicrobial and anticancer activity. After IFN-γ binds to the complex of IFN-γ receptor (IFNGR) 1-IFNGR2 and subsequently activates its downstream signaling pathways, IFN-γ immediately causes transcriptional stimulation of a variety of genes that are principally involved in its biological activities. Regarding IFN-γ-dependent immunosurveillance, IFN-γ can directly suppress tumorigenesis and infection and/or can modulate the immunological status in both cancer cells and infected cells. Regarding the anticancer effects of IFN-γ, cancer cells develop strategies to escape from IFN-γ-dependent cancer immunosurveillance. Immune evasion, including the recruitment of immunosuppressive cells, secretion of immunosuppressive factors, and suppression of cytotoxic T lymphocyte responses, is speculated to be elicited by the oncogenic microenvironment. All of these events effectively downregulate IFN-γ-expressing cells and IFN-γ production. In addition to these extrinsic pathways, cancer cells may develop cellular tolerance that manifests as hyporesponsiveness to IFN-γ stimulation. This review discusses the potential escape mechanisms from IFN-γ-dependent immunosurveillance in tumorigenesis. |
format | Online Article Text |
id | pubmed-5286687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52866872017-02-03 Escape from IFN-γ-dependent immunosurveillance in tumorigenesis Lin, Chiou-Feng Lin, Chih-Ming Lee, Kang-Yun Wu, Szu-Yuan Feng, Po-Hao Chen, Kuan-Yuan Chuang, Hsiao-Chi Chen, Chia-Ling Wang, Yu-Chih Tseng, Po-Chun Tsai, Tsung-Ting J Biomed Sci Review Immune interferon (IFN), also known as IFN-γ, promotes not only immunomodulation but also antimicrobial and anticancer activity. After IFN-γ binds to the complex of IFN-γ receptor (IFNGR) 1-IFNGR2 and subsequently activates its downstream signaling pathways, IFN-γ immediately causes transcriptional stimulation of a variety of genes that are principally involved in its biological activities. Regarding IFN-γ-dependent immunosurveillance, IFN-γ can directly suppress tumorigenesis and infection and/or can modulate the immunological status in both cancer cells and infected cells. Regarding the anticancer effects of IFN-γ, cancer cells develop strategies to escape from IFN-γ-dependent cancer immunosurveillance. Immune evasion, including the recruitment of immunosuppressive cells, secretion of immunosuppressive factors, and suppression of cytotoxic T lymphocyte responses, is speculated to be elicited by the oncogenic microenvironment. All of these events effectively downregulate IFN-γ-expressing cells and IFN-γ production. In addition to these extrinsic pathways, cancer cells may develop cellular tolerance that manifests as hyporesponsiveness to IFN-γ stimulation. This review discusses the potential escape mechanisms from IFN-γ-dependent immunosurveillance in tumorigenesis. BioMed Central 2017-02-01 /pmc/articles/PMC5286687/ /pubmed/28143527 http://dx.doi.org/10.1186/s12929-017-0317-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Lin, Chiou-Feng Lin, Chih-Ming Lee, Kang-Yun Wu, Szu-Yuan Feng, Po-Hao Chen, Kuan-Yuan Chuang, Hsiao-Chi Chen, Chia-Ling Wang, Yu-Chih Tseng, Po-Chun Tsai, Tsung-Ting Escape from IFN-γ-dependent immunosurveillance in tumorigenesis |
title | Escape from IFN-γ-dependent immunosurveillance in tumorigenesis |
title_full | Escape from IFN-γ-dependent immunosurveillance in tumorigenesis |
title_fullStr | Escape from IFN-γ-dependent immunosurveillance in tumorigenesis |
title_full_unstemmed | Escape from IFN-γ-dependent immunosurveillance in tumorigenesis |
title_short | Escape from IFN-γ-dependent immunosurveillance in tumorigenesis |
title_sort | escape from ifn-γ-dependent immunosurveillance in tumorigenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286687/ https://www.ncbi.nlm.nih.gov/pubmed/28143527 http://dx.doi.org/10.1186/s12929-017-0317-0 |
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