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Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma

Clear cell renal cell carcinoma (ccRCC) is widely acknowledged to be extremely sensitive to immunotherapy, emphasizing the tremendous impacts on which the tumor microenvironment (TME) has shown. However, the molecular subgroups characterized by the TME features scarcely serve as the risk stratificat...

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Autores principales: Zhang, Lu, Li, Jianlong, Zhang, Mengzhao, Wang, Lu, Yang, Tao, Shao, Qiuya, Liang, Xiao, Ma, Minghai, Zhang, Nan, Jing, Minxuan, Song, Rundong, Fan, Jinhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637193/
https://www.ncbi.nlm.nih.gov/pubmed/34868201
http://dx.doi.org/10.3389/fgene.2021.722421
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author Zhang, Lu
Li, Jianlong
Zhang, Mengzhao
Wang, Lu
Yang, Tao
Shao, Qiuya
Liang, Xiao
Ma, Minghai
Zhang, Nan
Jing, Minxuan
Song, Rundong
Fan, Jinhai
author_facet Zhang, Lu
Li, Jianlong
Zhang, Mengzhao
Wang, Lu
Yang, Tao
Shao, Qiuya
Liang, Xiao
Ma, Minghai
Zhang, Nan
Jing, Minxuan
Song, Rundong
Fan, Jinhai
author_sort Zhang, Lu
collection PubMed
description Clear cell renal cell carcinoma (ccRCC) is widely acknowledged to be extremely sensitive to immunotherapy, emphasizing the tremendous impacts on which the tumor microenvironment (TME) has shown. However, the molecular subgroups characterized by the TME features scarcely serve as the risk stratification guides in clinical practice for survival outcomes and immunotherapy response prediction. This study generated fresh insights into a novel TME-related prognostic signature derived from The Cancer Genome Atlas database using integrated bioinformatics analyses. Subsequently, Kaplan–Meier survival analysis, receiver operating characteristic analysis, and univariate and multivariate Cox regression analysis were performed to evaluate and validate the efficacy and the accuracy of the signature in ccRCC prognosis. Furthermore, we discovered that the risk score presented an increased likelihood of correlation with miscellaneous clinicopathological characteristics, natural killer cell-mediated cytotoxicity, immune cell infiltration levels, and immune checkpoint expression. These findings highlighted the notion that the six-gene signature characterized by the TME features may have implications on the risk stratification for personalized and precise immunotherapeutic management.
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spelling pubmed-86371932021-12-03 Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma Zhang, Lu Li, Jianlong Zhang, Mengzhao Wang, Lu Yang, Tao Shao, Qiuya Liang, Xiao Ma, Minghai Zhang, Nan Jing, Minxuan Song, Rundong Fan, Jinhai Front Genet Genetics Clear cell renal cell carcinoma (ccRCC) is widely acknowledged to be extremely sensitive to immunotherapy, emphasizing the tremendous impacts on which the tumor microenvironment (TME) has shown. However, the molecular subgroups characterized by the TME features scarcely serve as the risk stratification guides in clinical practice for survival outcomes and immunotherapy response prediction. This study generated fresh insights into a novel TME-related prognostic signature derived from The Cancer Genome Atlas database using integrated bioinformatics analyses. Subsequently, Kaplan–Meier survival analysis, receiver operating characteristic analysis, and univariate and multivariate Cox regression analysis were performed to evaluate and validate the efficacy and the accuracy of the signature in ccRCC prognosis. Furthermore, we discovered that the risk score presented an increased likelihood of correlation with miscellaneous clinicopathological characteristics, natural killer cell-mediated cytotoxicity, immune cell infiltration levels, and immune checkpoint expression. These findings highlighted the notion that the six-gene signature characterized by the TME features may have implications on the risk stratification for personalized and precise immunotherapeutic management. Frontiers Media S.A. 2021-11-18 /pmc/articles/PMC8637193/ /pubmed/34868201 http://dx.doi.org/10.3389/fgene.2021.722421 Text en Copyright © 2021 Zhang, Li, Zhang, Wang, Yang, Shao, Liang, Ma, Zhang, Jing, Song and Fan. 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 Genetics
Zhang, Lu
Li, Jianlong
Zhang, Mengzhao
Wang, Lu
Yang, Tao
Shao, Qiuya
Liang, Xiao
Ma, Minghai
Zhang, Nan
Jing, Minxuan
Song, Rundong
Fan, Jinhai
Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma
title Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma
title_full Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma
title_fullStr Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma
title_full_unstemmed Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma
title_short Identification of a Six-Gene Prognostic Signature Characterized by Tumor Microenvironment Immune Profiles in Clear Cell Renal Cell Carcinoma
title_sort identification of a six-gene prognostic signature characterized by tumor microenvironment immune profiles in clear cell renal cell carcinoma
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8637193/
https://www.ncbi.nlm.nih.gov/pubmed/34868201
http://dx.doi.org/10.3389/fgene.2021.722421
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