Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma

Tumor immune microenvironment (TIME) plays an important role in tumor diagnosis, prevention, treatment and prognosis. However, the correlation and potential mechanism between clear cell renal cell carcinoma (ccRCC) and its TIME are not clear. Therefore, we aimed to identify potential prognostic biom...

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Main Authors: Jingwei Ke, Jie Chen, Xin Liu
Format: Article
Language:English
Published: Taylor & Francis Group 2022-03-01
Series:Animal Cells and Systems
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/19768354.2022.2056635
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author Jingwei Ke
Jie Chen
Xin Liu
author_facet Jingwei Ke
Jie Chen
Xin Liu
author_sort Jingwei Ke
collection DOAJ
description Tumor immune microenvironment (TIME) plays an important role in tumor diagnosis, prevention, treatment and prognosis. However, the correlation and potential mechanism between clear cell renal cell carcinoma (ccRCC) and its TIME are not clear. Therefore, we aimed to identify potential prognostic biomarkers related to TIME of ccRCC. Unsupervised consensus clustering analysis was performed to divide patients into different immune subgroups according to their single-sample gene set enrichment analysis (ssGSEA) scores. Then, we validated the differences in immune cell infiltration, prognosis, clinical characteristics and expression levels of HLA and immune checkpoint genes between different immune subgroups. Weighted gene coexpression network analysis (WGCNA) was used to identify the significant modules and hub genes that were related to the immune subgroups. A nomogram was established to predict the overall survival (OS) outcomes after independent prognostic factors were identified by least absolute shrinkage and selection operator (LASSO) regression and multivariate Cox regression analyses. Five clusters (immune subgroups) were identified. There was no significant difference in age, sex or N stage. And there were significant differences in race, T stage, M stage, grade, prognosis and tumor microenvironment. WGCNA revealed that the red module has an important relationship with TIME, and obtained 14 hub genes. In addition, the nomogram containing LAG3 and GZMK accurately predicted OS outcomes of ccRCC patients. LAG3 and GZMK have a certain correlation with the prognosis of ccRCC patients, and play an important role in the TIME. These two hub genes deserve further study as biomarkers of the TIME.
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spelling doaj.art-3ff0cddcfcbd440e811063dbd82aec172022-12-22T02:03:40ZengTaylor & Francis GroupAnimal Cells and Systems1976-83542151-24852022-03-01262526110.1080/19768354.2022.2056635Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinomaJingwei Ke0Jie Chen1Xin Liu2Department of urology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, People’s Republic of ChinaGraduate School of Southwest Medical University, Luzhou, People’s Republic of ChinaDepartment of urology, The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University, Luzhou, People’s Republic of ChinaTumor immune microenvironment (TIME) plays an important role in tumor diagnosis, prevention, treatment and prognosis. However, the correlation and potential mechanism between clear cell renal cell carcinoma (ccRCC) and its TIME are not clear. Therefore, we aimed to identify potential prognostic biomarkers related to TIME of ccRCC. Unsupervised consensus clustering analysis was performed to divide patients into different immune subgroups according to their single-sample gene set enrichment analysis (ssGSEA) scores. Then, we validated the differences in immune cell infiltration, prognosis, clinical characteristics and expression levels of HLA and immune checkpoint genes between different immune subgroups. Weighted gene coexpression network analysis (WGCNA) was used to identify the significant modules and hub genes that were related to the immune subgroups. A nomogram was established to predict the overall survival (OS) outcomes after independent prognostic factors were identified by least absolute shrinkage and selection operator (LASSO) regression and multivariate Cox regression analyses. Five clusters (immune subgroups) were identified. There was no significant difference in age, sex or N stage. And there were significant differences in race, T stage, M stage, grade, prognosis and tumor microenvironment. WGCNA revealed that the red module has an important relationship with TIME, and obtained 14 hub genes. In addition, the nomogram containing LAG3 and GZMK accurately predicted OS outcomes of ccRCC patients. LAG3 and GZMK have a certain correlation with the prognosis of ccRCC patients, and play an important role in the TIME. These two hub genes deserve further study as biomarkers of the TIME.https://www.tandfonline.com/doi/10.1080/19768354.2022.2056635Clear cell renal cell carcinomamicroenvironmentprognosisnomogrambioinformatics
spellingShingle Jingwei Ke
Jie Chen
Xin Liu
Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
Animal Cells and Systems
Clear cell renal cell carcinoma
microenvironment
prognosis
nomogram
bioinformatics
title Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
title_full Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
title_fullStr Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
title_full_unstemmed Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
title_short Analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
title_sort analyzing and validating the prognostic value and immune microenvironment of clear cell renal cell carcinoma
topic Clear cell renal cell carcinoma
microenvironment
prognosis
nomogram
bioinformatics
url https://www.tandfonline.com/doi/10.1080/19768354.2022.2056635
work_keys_str_mv AT jingweike analyzingandvalidatingtheprognosticvalueandimmunemicroenvironmentofclearcellrenalcellcarcinoma
AT jiechen analyzingandvalidatingtheprognosticvalueandimmunemicroenvironmentofclearcellrenalcellcarcinoma
AT xinliu analyzingandvalidatingtheprognosticvalueandimmunemicroenvironmentofclearcellrenalcellcarcinoma