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The immune contexture of hepatocellular carcinoma predicts clinical outcome
The general relevance of the immune system for cancer development and therapy is increasingly recognized. However and although the immune contexture of most human cancer types has been determined, a global characterisation of the immune tumour microenvironment in hepatocellular carcinoma (HCC) is la...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876395/ https://www.ncbi.nlm.nih.gov/pubmed/29599491 http://dx.doi.org/10.1038/s41598-018-21937-2 |
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author | Foerster, Friedrich Hess, Moritz Gerhold-Ay, Aslihan Marquardt, Jens Uwe Becker, Diana Galle, Peter Robert Schuppan, Detlef Binder, Harald Bockamp, Ernesto |
author_facet | Foerster, Friedrich Hess, Moritz Gerhold-Ay, Aslihan Marquardt, Jens Uwe Becker, Diana Galle, Peter Robert Schuppan, Detlef Binder, Harald Bockamp, Ernesto |
author_sort | Foerster, Friedrich |
collection | PubMed |
description | The general relevance of the immune system for cancer development and therapy is increasingly recognized. However and although the immune contexture of most human cancer types has been determined, a global characterisation of the immune tumour microenvironment in hepatocellular carcinoma (HCC) is lacking. Equally, differences in the immune contexture of HCC between different patient subgroups and its effect on survival remain to be established. Here we report an in silico analysis of the immune contexture of human HCC. Using large deep sequencing HCC tumour, adjacent non-tumour and healthy liver high-dimensional data sets, we were able to reveal previously unrecognized differences in the immune contexture of HCC. Strikingly, we found that different etiologies and HCC stages were not associated with major changes in the immune contexture. In contrast, the presence of T cells and cytotoxic cells as well as the absence of macrophages and Th2 cells positively correlated with patient survival. Based on these novel findings, we developed a prognostic score that accurately distinguishes between patients with good and poor survival. Our study provides the first global characterisation of the immune contexture of HCC and will have direct implications for future HCC therapies. |
format | Online Article Text |
id | pubmed-5876395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58763952018-04-02 The immune contexture of hepatocellular carcinoma predicts clinical outcome Foerster, Friedrich Hess, Moritz Gerhold-Ay, Aslihan Marquardt, Jens Uwe Becker, Diana Galle, Peter Robert Schuppan, Detlef Binder, Harald Bockamp, Ernesto Sci Rep Article The general relevance of the immune system for cancer development and therapy is increasingly recognized. However and although the immune contexture of most human cancer types has been determined, a global characterisation of the immune tumour microenvironment in hepatocellular carcinoma (HCC) is lacking. Equally, differences in the immune contexture of HCC between different patient subgroups and its effect on survival remain to be established. Here we report an in silico analysis of the immune contexture of human HCC. Using large deep sequencing HCC tumour, adjacent non-tumour and healthy liver high-dimensional data sets, we were able to reveal previously unrecognized differences in the immune contexture of HCC. Strikingly, we found that different etiologies and HCC stages were not associated with major changes in the immune contexture. In contrast, the presence of T cells and cytotoxic cells as well as the absence of macrophages and Th2 cells positively correlated with patient survival. Based on these novel findings, we developed a prognostic score that accurately distinguishes between patients with good and poor survival. Our study provides the first global characterisation of the immune contexture of HCC and will have direct implications for future HCC therapies. Nature Publishing Group UK 2018-03-29 /pmc/articles/PMC5876395/ /pubmed/29599491 http://dx.doi.org/10.1038/s41598-018-21937-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Foerster, Friedrich Hess, Moritz Gerhold-Ay, Aslihan Marquardt, Jens Uwe Becker, Diana Galle, Peter Robert Schuppan, Detlef Binder, Harald Bockamp, Ernesto The immune contexture of hepatocellular carcinoma predicts clinical outcome |
title | The immune contexture of hepatocellular carcinoma predicts clinical outcome |
title_full | The immune contexture of hepatocellular carcinoma predicts clinical outcome |
title_fullStr | The immune contexture of hepatocellular carcinoma predicts clinical outcome |
title_full_unstemmed | The immune contexture of hepatocellular carcinoma predicts clinical outcome |
title_short | The immune contexture of hepatocellular carcinoma predicts clinical outcome |
title_sort | immune contexture of hepatocellular carcinoma predicts clinical outcome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876395/ https://www.ncbi.nlm.nih.gov/pubmed/29599491 http://dx.doi.org/10.1038/s41598-018-21937-2 |
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