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Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study
Mounting evidence supports that the malignant phenotypes of cancers are defined not only by the intrinsic activity of tumor cells but also by immune cells that are recruited and activated in tumor-related microenvironment. Here, we developed a diagnostic and prognostic model for colon cancer, based...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227137/ https://www.ncbi.nlm.nih.gov/pubmed/32457797 http://dx.doi.org/10.3389/fgene.2020.00401 |
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author | Yang, Haojie Jin, Wei Liu, Hua Gan, Dan Cui, Can Han, Changpeng Wang, Zhenyi |
author_facet | Yang, Haojie Jin, Wei Liu, Hua Gan, Dan Cui, Can Han, Changpeng Wang, Zhenyi |
author_sort | Yang, Haojie |
collection | PubMed |
description | Mounting evidence supports that the malignant phenotypes of cancers are defined not only by the intrinsic activity of tumor cells but also by immune cells that are recruited and activated in tumor-related microenvironment. Here, we developed a diagnostic and prognostic model for colon cancer, based on expression profiles of immune-related genes and immune cell component. As a result, we found that B cell infiltration ratio, CD4(+) T cells, as well as immune-related genes of TRIB3, CHGA, CASP7, LGALS4, LEP, NOX4, IL17A, and HSPD1 may be highly relevant with clinical outcome of colon cancer. |
format | Online Article Text |
id | pubmed-7227137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72271372020-05-25 Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study Yang, Haojie Jin, Wei Liu, Hua Gan, Dan Cui, Can Han, Changpeng Wang, Zhenyi Front Genet Genetics Mounting evidence supports that the malignant phenotypes of cancers are defined not only by the intrinsic activity of tumor cells but also by immune cells that are recruited and activated in tumor-related microenvironment. Here, we developed a diagnostic and prognostic model for colon cancer, based on expression profiles of immune-related genes and immune cell component. As a result, we found that B cell infiltration ratio, CD4(+) T cells, as well as immune-related genes of TRIB3, CHGA, CASP7, LGALS4, LEP, NOX4, IL17A, and HSPD1 may be highly relevant with clinical outcome of colon cancer. Frontiers Media S.A. 2020-05-08 /pmc/articles/PMC7227137/ /pubmed/32457797 http://dx.doi.org/10.3389/fgene.2020.00401 Text en Copyright © 2020 Yang, Jin, Liu, Gan, Cui, Han and Wang. http://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(s) 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 | Genetics Yang, Haojie Jin, Wei Liu, Hua Gan, Dan Cui, Can Han, Changpeng Wang, Zhenyi Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study |
title | Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study |
title_full | Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study |
title_fullStr | Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study |
title_full_unstemmed | Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study |
title_short | Immune-Related Prognostic Model in Colon Cancer: A Gene Expression-Based Study |
title_sort | immune-related prognostic model in colon cancer: a gene expression-based study |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7227137/ https://www.ncbi.nlm.nih.gov/pubmed/32457797 http://dx.doi.org/10.3389/fgene.2020.00401 |
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