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Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer
BACKGROUND: Renal cell carcinoma (RCC) is associated with poor prognostic outcomes. The current stratifying system does not predict prognostic outcomes and therapeutic benefits precisely for RCC patients. Here, we aim to construct an immune prognostic predictive model to assist clinician to predict...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546215/ https://www.ncbi.nlm.nih.gov/pubmed/34712244 http://dx.doi.org/10.3389/fimmu.2021.762120 |
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author | Feng, Tao Zhao, Jiahui Wei, Dechao Guo, Pengju Yang, Xiaobing Li, Qiankun Fang, Zhou Wei, Ziheng Li, Mingchuan Jiang, Yongguang Luo, Yong |
author_facet | Feng, Tao Zhao, Jiahui Wei, Dechao Guo, Pengju Yang, Xiaobing Li, Qiankun Fang, Zhou Wei, Ziheng Li, Mingchuan Jiang, Yongguang Luo, Yong |
author_sort | Feng, Tao |
collection | PubMed |
description | BACKGROUND: Renal cell carcinoma (RCC) is associated with poor prognostic outcomes. The current stratifying system does not predict prognostic outcomes and therapeutic benefits precisely for RCC patients. Here, we aim to construct an immune prognostic predictive model to assist clinician to predict RCC prognosis. METHODS: Herein, an immune prognostic signature was developed, and its predictive ability was confirmed in the kidney renal clear cell carcinoma (KIRC) cohorts based on The Cancer Genome Atlas (TCGA) dataset. Several immunogenomic analyses were conducted to investigate the correlations between immune risk scores and immune cell infiltrations, immune checkpoints, cancer genotypes, tumor mutational burden, and responses to chemotherapy and immunotherapy. RESULTS: The immune prognostic signature contained 14 immune-associated genes and was found to be an independent prognostic factor for KIRC. Furthermore, the immune risk score was established as a novel marker for predicting the overall survival outcomes for RCC. The risk score was correlated with some significant immunophenotypic factors, including T cell infiltration, antitumor immunity, antitumor response, oncogenic pathways, and immunotherapeutic and chemotherapeutic response. CONCLUSIONS: The immune prognostic, predictive model can be effectively and efficiently used in the prediction of survival outcomes and immunotherapeutic responses of RCC patients. |
format | Online Article Text |
id | pubmed-8546215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85462152021-10-27 Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer Feng, Tao Zhao, Jiahui Wei, Dechao Guo, Pengju Yang, Xiaobing Li, Qiankun Fang, Zhou Wei, Ziheng Li, Mingchuan Jiang, Yongguang Luo, Yong Front Immunol Immunology BACKGROUND: Renal cell carcinoma (RCC) is associated with poor prognostic outcomes. The current stratifying system does not predict prognostic outcomes and therapeutic benefits precisely for RCC patients. Here, we aim to construct an immune prognostic predictive model to assist clinician to predict RCC prognosis. METHODS: Herein, an immune prognostic signature was developed, and its predictive ability was confirmed in the kidney renal clear cell carcinoma (KIRC) cohorts based on The Cancer Genome Atlas (TCGA) dataset. Several immunogenomic analyses were conducted to investigate the correlations between immune risk scores and immune cell infiltrations, immune checkpoints, cancer genotypes, tumor mutational burden, and responses to chemotherapy and immunotherapy. RESULTS: The immune prognostic signature contained 14 immune-associated genes and was found to be an independent prognostic factor for KIRC. Furthermore, the immune risk score was established as a novel marker for predicting the overall survival outcomes for RCC. The risk score was correlated with some significant immunophenotypic factors, including T cell infiltration, antitumor immunity, antitumor response, oncogenic pathways, and immunotherapeutic and chemotherapeutic response. CONCLUSIONS: The immune prognostic, predictive model can be effectively and efficiently used in the prediction of survival outcomes and immunotherapeutic responses of RCC patients. Frontiers Media S.A. 2021-10-12 /pmc/articles/PMC8546215/ /pubmed/34712244 http://dx.doi.org/10.3389/fimmu.2021.762120 Text en Copyright © 2021 Feng, Zhao, Wei, Guo, Yang, Li, Fang, Wei, Li, Jiang and Luo https://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 | Immunology Feng, Tao Zhao, Jiahui Wei, Dechao Guo, Pengju Yang, Xiaobing Li, Qiankun Fang, Zhou Wei, Ziheng Li, Mingchuan Jiang, Yongguang Luo, Yong Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer |
title | Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer |
title_full | Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer |
title_fullStr | Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer |
title_full_unstemmed | Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer |
title_short | Immunogenomic Analyses of the Prognostic Predictive Model for Patients With Renal Cancer |
title_sort | immunogenomic analyses of the prognostic predictive model for patients with renal cancer |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546215/ https://www.ncbi.nlm.nih.gov/pubmed/34712244 http://dx.doi.org/10.3389/fimmu.2021.762120 |
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