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Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy

The clear cell renal cell carcinoma (ccRCC) is the main pathological subtype of renal cell carcinoma. Immune system evasion, one hallmark of cancer, contributes to cancer cells in escaping from the attack of immune cells. In order to identify potential prognostic biomarkers in ccRCC patients and imm...

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Autores principales: Xiang, Zhenfei, Shen, Erdong, Li, Mingyao, Hu, Danfei, Zhang, Zhanchun, Yu, Senquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806734/
https://www.ncbi.nlm.nih.gov/pubmed/34002666
http://dx.doi.org/10.1080/21655979.2021.1924546
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author Xiang, Zhenfei
Shen, Erdong
Li, Mingyao
Hu, Danfei
Zhang, Zhanchun
Yu, Senquan
author_facet Xiang, Zhenfei
Shen, Erdong
Li, Mingyao
Hu, Danfei
Zhang, Zhanchun
Yu, Senquan
author_sort Xiang, Zhenfei
collection PubMed
description The clear cell renal cell carcinoma (ccRCC) is the main pathological subtype of renal cell carcinoma. Immune system evasion, one hallmark of cancer, contributes to cancer cells in escaping from the attack of immune cells. In order to identify potential prognostic biomarkers in ccRCC patients and immune cells fraction, we collected and downloaded profiles from The Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO) database. We obtained 2 modules significantly associated with tumor stage and immune cells; functional enrichment analysis showed that genes in the module ‘yellow’ were significantly enriched in proteins targeting to membrane and ribosome, as well as the oxidative phosphorylation pathway, while genes in the module ‘green’ mainly participate in molecular functions associated with immunity like activation of T cells. Four LncRNAs (LINC00472, AL590094.1, AL365203.3, and AC147651.3) and RPL27A and RPL22L1 in the module ‘yellow’ and two lncRNAs (LINC00426 and AC129507.2) and five protein-coding genes (CSF1, NOD2, ITGAE, CD7, and PDCD1) in the module ‘green’ represented independent prognostic values in patients with ccRCC. Expression of LINC0042, NOD2, CD7, and PDCD1 were significantly correlated with ratio of immune cells (like T cells CD8 and resting mast cells). LINC00426, with significant correlation with immune cell fraction, shows potential prognostic value in ccRCC patients. Our findings provide a strategy in exploring biomarkers with prognostic significance and significant association with the fraction of immune cells.
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spelling pubmed-88067342022-02-02 Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy Xiang, Zhenfei Shen, Erdong Li, Mingyao Hu, Danfei Zhang, Zhanchun Yu, Senquan Bioengineered Research Paper The clear cell renal cell carcinoma (ccRCC) is the main pathological subtype of renal cell carcinoma. Immune system evasion, one hallmark of cancer, contributes to cancer cells in escaping from the attack of immune cells. In order to identify potential prognostic biomarkers in ccRCC patients and immune cells fraction, we collected and downloaded profiles from The Cancer Genome Atlas (TCGA) database and Gene Expression Omnibus (GEO) database. We obtained 2 modules significantly associated with tumor stage and immune cells; functional enrichment analysis showed that genes in the module ‘yellow’ were significantly enriched in proteins targeting to membrane and ribosome, as well as the oxidative phosphorylation pathway, while genes in the module ‘green’ mainly participate in molecular functions associated with immunity like activation of T cells. Four LncRNAs (LINC00472, AL590094.1, AL365203.3, and AC147651.3) and RPL27A and RPL22L1 in the module ‘yellow’ and two lncRNAs (LINC00426 and AC129507.2) and five protein-coding genes (CSF1, NOD2, ITGAE, CD7, and PDCD1) in the module ‘green’ represented independent prognostic values in patients with ccRCC. Expression of LINC0042, NOD2, CD7, and PDCD1 were significantly correlated with ratio of immune cells (like T cells CD8 and resting mast cells). LINC00426, with significant correlation with immune cell fraction, shows potential prognostic value in ccRCC patients. Our findings provide a strategy in exploring biomarkers with prognostic significance and significant association with the fraction of immune cells. Taylor & Francis 2021-05-18 /pmc/articles/PMC8806734/ /pubmed/34002666 http://dx.doi.org/10.1080/21655979.2021.1924546 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Xiang, Zhenfei
Shen, Erdong
Li, Mingyao
Hu, Danfei
Zhang, Zhanchun
Yu, Senquan
Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
title Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
title_full Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
title_fullStr Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
title_full_unstemmed Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
title_short Potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
title_sort potential prognostic biomarkers related to immunity in clear cell renal cell carcinoma using bioinformatic strategy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8806734/
https://www.ncbi.nlm.nih.gov/pubmed/34002666
http://dx.doi.org/10.1080/21655979.2021.1924546
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