Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis

Backgrounds: To screen biomarkers related to clear cell renal cell carcinoma (ccRCC) progression and prognosis. Methods: 1,026 ccRCC-related genes were dug from 494 ccRCC samples in TCGA based on weighted gene co-expression network analysis, and 7 modules were identified. Afterwards, GO and KEGG enr...

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Autores principales: Xiaoxia Yu, Hua Wu, Hongmei Wang, He Dong, Bihu Gao
Formato: article
Lenguaje:EN
Publicado: Karger Publishers 2021
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spelling oai:doaj.org-article:bf925408642f4dc89481cbc09f2399fd2021-12-02T12:40:22ZIdentification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis1420-40961423-014310.1159/000520832https://doaj.org/article/bf925408642f4dc89481cbc09f2399fd2021-11-01T00:00:00Zhttps://www.karger.com/Article/FullText/520832https://doaj.org/toc/1420-4096https://doaj.org/toc/1423-0143Backgrounds: To screen biomarkers related to clear cell renal cell carcinoma (ccRCC) progression and prognosis. Methods: 1,026 ccRCC-related genes were dug from 494 ccRCC samples in TCGA based on weighted gene co-expression network analysis, and 7 modules were identified. Afterwards, GO and KEGG enrichment analyses were conducted on modules of interest. Genes in these modules were taken as the input to construct a protein-protein interaction network. Thereafter, 30 genes with the highest connectivity were taken as core genes. Univariate Cox regression, LASSO Cox regression and multivariate Cox regression analyses were performed on core genes. Univariate and multivariate Cox regression analyses were performed on patient’s clinical characteristics and risk scores. Results: Stage displayed significantly strong correlations with green module and red module (p<0.001). Genes in modules participated in biological functions including T cell proliferation and regulation of lymphocyte activation. GSEA showed that high- and low-risk groups exhibited significant enrichment differences in pathways related to immunity, cell migration and invasion. Immune infiltration analysis also presented strong correlation between expression of these 8 genes and immune cell infiltration in ccRCC samples. It was displayed that risk score could be an independent factor to assess patient’s prognosis. Conclusion: We determined biomarkers relevant to ccRCC progression, offering candidate targets for ccRCC treatment.Xiaoxia YuHua WuHongmei WangHe DongBihu GaoKarger PublishersarticleDermatologyRL1-803Diseases of the circulatory (Cardiovascular) systemRC666-701Diseases of the genitourinary system. UrologyRC870-923ENKidney & Blood Pressure Research (2021)
institution DOAJ
collection DOAJ
language EN
topic Dermatology
RL1-803
Diseases of the circulatory (Cardiovascular) system
RC666-701
Diseases of the genitourinary system. Urology
RC870-923
spellingShingle Dermatology
RL1-803
Diseases of the circulatory (Cardiovascular) system
RC666-701
Diseases of the genitourinary system. Urology
RC870-923
Xiaoxia Yu
Hua Wu
Hongmei Wang
He Dong
Bihu Gao
Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
description Backgrounds: To screen biomarkers related to clear cell renal cell carcinoma (ccRCC) progression and prognosis. Methods: 1,026 ccRCC-related genes were dug from 494 ccRCC samples in TCGA based on weighted gene co-expression network analysis, and 7 modules were identified. Afterwards, GO and KEGG enrichment analyses were conducted on modules of interest. Genes in these modules were taken as the input to construct a protein-protein interaction network. Thereafter, 30 genes with the highest connectivity were taken as core genes. Univariate Cox regression, LASSO Cox regression and multivariate Cox regression analyses were performed on core genes. Univariate and multivariate Cox regression analyses were performed on patient’s clinical characteristics and risk scores. Results: Stage displayed significantly strong correlations with green module and red module (p<0.001). Genes in modules participated in biological functions including T cell proliferation and regulation of lymphocyte activation. GSEA showed that high- and low-risk groups exhibited significant enrichment differences in pathways related to immunity, cell migration and invasion. Immune infiltration analysis also presented strong correlation between expression of these 8 genes and immune cell infiltration in ccRCC samples. It was displayed that risk score could be an independent factor to assess patient’s prognosis. Conclusion: We determined biomarkers relevant to ccRCC progression, offering candidate targets for ccRCC treatment.
format article
author Xiaoxia Yu
Hua Wu
Hongmei Wang
He Dong
Bihu Gao
author_facet Xiaoxia Yu
Hua Wu
Hongmei Wang
He Dong
Bihu Gao
author_sort Xiaoxia Yu
title Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
title_short Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
title_full Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
title_fullStr Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
title_full_unstemmed Identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
title_sort identification of 8 feature genes related to clear cell renal cell carcinoma progression based on co-expression analysis
publisher Karger Publishers
publishDate 2021
url https://doaj.org/article/bf925408642f4dc89481cbc09f2399fd
work_keys_str_mv AT xiaoxiayu identificationof8featuregenesrelatedtoclearcellrenalcellcarcinomaprogressionbasedoncoexpressionanalysis
AT huawu identificationof8featuregenesrelatedtoclearcellrenalcellcarcinomaprogressionbasedoncoexpressionanalysis
AT hongmeiwang identificationof8featuregenesrelatedtoclearcellrenalcellcarcinomaprogressionbasedoncoexpressionanalysis
AT hedong identificationof8featuregenesrelatedtoclearcellrenalcellcarcinomaprogressionbasedoncoexpressionanalysis
AT bihugao identificationof8featuregenesrelatedtoclearcellrenalcellcarcinomaprogressionbasedoncoexpressionanalysis
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