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Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis

Cancer, especially malignant tumors with poor prognosis, has become a major hazard to human life and health. The tumor microenvironment is gaining increasing attention from researchers, as it offers a new focus for tumor diagnosis, therapy, and prognosis. The numbers of immune and stromal cells, whi...

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Autores principales: Liu, Yu, Zhou, Hao, Zheng, Ji, Zeng, Xiaojun, Yu, Wenjing, Liu, Wei, Huang, Guorong, Zhang, Yang, Fu, Weiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438715/
https://www.ncbi.nlm.nih.gov/pubmed/32903590
http://dx.doi.org/10.3389/fonc.2020.01008
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author Liu, Yu
Zhou, Hao
Zheng, Ji
Zeng, Xiaojun
Yu, Wenjing
Liu, Wei
Huang, Guorong
Zhang, Yang
Fu, Weiling
author_facet Liu, Yu
Zhou, Hao
Zheng, Ji
Zeng, Xiaojun
Yu, Wenjing
Liu, Wei
Huang, Guorong
Zhang, Yang
Fu, Weiling
author_sort Liu, Yu
collection PubMed
description Cancer, especially malignant tumors with poor prognosis, has become a major hazard to human life and health. The tumor microenvironment is gaining increasing attention from researchers, as it offers a new focus for tumor diagnosis, therapy, and prognosis. The numbers of immune and stromal cells, which are major components of the tumor microenvironment, could be determined from RNA-seq data with the Estimation of STromal and Immune cells in Malignant Tumors using Expression data (ESTIMATE) algorithm. To explore the effects of immune and stromal cells on tumor prognosis, we analyzed associations between overall survival and immune/stromal scores for 20 malignant tumor types based on The Cancer Genome Atlas (TCGA) data. For six of the 20 tumor types, we observed statistically significant associations. Furthermore, to better explain the predictive ability of these scores, differentially expressed genes (DEGs) were identified in groups of cases with high or low immune or stromal scores for each of these six malignant tumor types. In addition, a list of immune-related genes was screened to identify prognostic predictors for one or more tumor types. Thus, multi-database joint analysis can provide a new approach to the assessment of tumor prognosis and allow the identification of related genes that may be new biomarkers for tumor metastasis and prognosis.
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spelling pubmed-74387152020-09-03 Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis Liu, Yu Zhou, Hao Zheng, Ji Zeng, Xiaojun Yu, Wenjing Liu, Wei Huang, Guorong Zhang, Yang Fu, Weiling Front Oncol Oncology Cancer, especially malignant tumors with poor prognosis, has become a major hazard to human life and health. The tumor microenvironment is gaining increasing attention from researchers, as it offers a new focus for tumor diagnosis, therapy, and prognosis. The numbers of immune and stromal cells, which are major components of the tumor microenvironment, could be determined from RNA-seq data with the Estimation of STromal and Immune cells in Malignant Tumors using Expression data (ESTIMATE) algorithm. To explore the effects of immune and stromal cells on tumor prognosis, we analyzed associations between overall survival and immune/stromal scores for 20 malignant tumor types based on The Cancer Genome Atlas (TCGA) data. For six of the 20 tumor types, we observed statistically significant associations. Furthermore, to better explain the predictive ability of these scores, differentially expressed genes (DEGs) were identified in groups of cases with high or low immune or stromal scores for each of these six malignant tumor types. In addition, a list of immune-related genes was screened to identify prognostic predictors for one or more tumor types. Thus, multi-database joint analysis can provide a new approach to the assessment of tumor prognosis and allow the identification of related genes that may be new biomarkers for tumor metastasis and prognosis. Frontiers Media S.A. 2020-07-31 /pmc/articles/PMC7438715/ /pubmed/32903590 http://dx.doi.org/10.3389/fonc.2020.01008 Text en Copyright © 2020 Liu, Zhou, Zheng, Zeng, Yu, Liu, Huang, Zhang and Fu. 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 Oncology
Liu, Yu
Zhou, Hao
Zheng, Ji
Zeng, Xiaojun
Yu, Wenjing
Liu, Wei
Huang, Guorong
Zhang, Yang
Fu, Weiling
Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis
title Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis
title_full Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis
title_fullStr Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis
title_full_unstemmed Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis
title_short Identification of Immune-Related Prognostic Biomarkers Based on the Tumor Microenvironment in 20 Malignant Tumor Types With Poor Prognosis
title_sort identification of immune-related prognostic biomarkers based on the tumor microenvironment in 20 malignant tumor types with poor prognosis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7438715/
https://www.ncbi.nlm.nih.gov/pubmed/32903590
http://dx.doi.org/10.3389/fonc.2020.01008
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