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Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer
Background: Colorectal cancer (CRC) accounts for the highest fatality rate among all malignant tumors. Immunotherapy has shown great promise in management of many malignant tumors, necessitating the need to explore its role in CRC. Results: Our analysis revealed a total of 71 differentially expresse...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185108/ https://www.ncbi.nlm.nih.gov/pubmed/32235004 http://dx.doi.org/10.18632/aging.102979 |
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author | Lin, Kang Huang, Jun Luo, Hongliang Luo, Chen Zhu, Xiaojian Bu, Fanqin Xiao, Han Xiao, Li Zhu, Zhengming |
author_facet | Lin, Kang Huang, Jun Luo, Hongliang Luo, Chen Zhu, Xiaojian Bu, Fanqin Xiao, Han Xiao, Li Zhu, Zhengming |
author_sort | Lin, Kang |
collection | PubMed |
description | Background: Colorectal cancer (CRC) accounts for the highest fatality rate among all malignant tumors. Immunotherapy has shown great promise in management of many malignant tumors, necessitating the need to explore its role in CRC. Results: Our analysis revealed a total of 71 differentially expressed IRGs, that were associated with prognosis of CRC patients. Ten IRGs (FABP4, IGKV1-33, IGKV2D-40, IGLV6-57, NGF, RETNLB, UCN, VIP, NGFR, and OXTR) showed high prognostic performance in predicting CRC outcomes, and were further associated with tumor burden, metastasis, tumor TNM stage, gender, age, and pathological stage. Interestingly, the IRG-based prognostic index (IRGPI) reflected infiltration of multiple immune cell types. Conclusions: This model provides an effective approach for stratification and characterization of patients using IRG-based immunolabeling tools to monitor prognosis of CRC. Methods: We performed a comprehensive analysis of expression profiles for immune-related genes (IRGs) and overall survival time in 437 CRC patients from the TCGA database. We employed computational algorithms and Cox regression analysis to estimate the relationship between differentially expressed IRGs and survival rates in CRC patients. Furthermore, we investigated the mechanisms of action of the IRGs involved in CRC, and established a novel prognostic index based on multivariate Cox models. |
format | Online Article Text |
id | pubmed-7185108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-71851082020-05-01 Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer Lin, Kang Huang, Jun Luo, Hongliang Luo, Chen Zhu, Xiaojian Bu, Fanqin Xiao, Han Xiao, Li Zhu, Zhengming Aging (Albany NY) Research Paper Background: Colorectal cancer (CRC) accounts for the highest fatality rate among all malignant tumors. Immunotherapy has shown great promise in management of many malignant tumors, necessitating the need to explore its role in CRC. Results: Our analysis revealed a total of 71 differentially expressed IRGs, that were associated with prognosis of CRC patients. Ten IRGs (FABP4, IGKV1-33, IGKV2D-40, IGLV6-57, NGF, RETNLB, UCN, VIP, NGFR, and OXTR) showed high prognostic performance in predicting CRC outcomes, and were further associated with tumor burden, metastasis, tumor TNM stage, gender, age, and pathological stage. Interestingly, the IRG-based prognostic index (IRGPI) reflected infiltration of multiple immune cell types. Conclusions: This model provides an effective approach for stratification and characterization of patients using IRG-based immunolabeling tools to monitor prognosis of CRC. Methods: We performed a comprehensive analysis of expression profiles for immune-related genes (IRGs) and overall survival time in 437 CRC patients from the TCGA database. We employed computational algorithms and Cox regression analysis to estimate the relationship between differentially expressed IRGs and survival rates in CRC patients. Furthermore, we investigated the mechanisms of action of the IRGs involved in CRC, and established a novel prognostic index based on multivariate Cox models. Impact Journals 2020-03-31 /pmc/articles/PMC7185108/ /pubmed/32235004 http://dx.doi.org/10.18632/aging.102979 Text en Copyright © 2020 Lin et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Lin, Kang Huang, Jun Luo, Hongliang Luo, Chen Zhu, Xiaojian Bu, Fanqin Xiao, Han Xiao, Li Zhu, Zhengming Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
title | Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
title_full | Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
title_fullStr | Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
title_full_unstemmed | Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
title_short | Development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
title_sort | development of a prognostic index and screening of potential biomarkers based on immunogenomic landscape analysis of colorectal cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7185108/ https://www.ncbi.nlm.nih.gov/pubmed/32235004 http://dx.doi.org/10.18632/aging.102979 |
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