CARD11 is a prognostic biomarker and correlated with immune infiltrates in uveal melanoma

Uveal melanoma (UVM), the most common primary intraocular malignancy, has a high mortality because of a high propensity to metastasize. Our study analyzed prognostic value and immune-related characteristics of CARD11 in UVM, hoping to provide a potential management and research direction. The RNA-se...

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Veröffentlicht in:PloS one 2021-08, Vol.16 (8), p.e0255293
Hauptverfasser: Shi, Xueying, Xia, Shilin, Chu, Yingming, Yang, Nan, Zheng, Jingyuan, Chen, Qianyi, Fen, Zeng, Jiang, Yuankuan, Fang, Shifeng, Lin, Jingrong
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creator Shi, Xueying
Xia, Shilin
Chu, Yingming
Yang, Nan
Zheng, Jingyuan
Chen, Qianyi
Fen, Zeng
Jiang, Yuankuan
Fang, Shifeng
Lin, Jingrong
description Uveal melanoma (UVM), the most common primary intraocular malignancy, has a high mortality because of a high propensity to metastasize. Our study analyzed prognostic value and immune-related characteristics of CARD11 in UVM, hoping to provide a potential management and research direction. The RNA-sequence data of 80 UVM patients were downloaded from The Cancer Genome Atlas database and divided them into high- and low-expression groups. We analyzed the differentially expressed genes, enrichment analyses and the infiltration of immune cells using the R package and Gene-Set Enrichment Analysis. A clinical prediction nomogram and protein-protein interaction network were constructed and the first 8 genes were considered as the hub-genes. Finally, we constructed a competing endogenous RNA (ceRNA) network by Cytoscape and analyzed the statistical data via the R software. Here we found that CARD11 expression had notable correlation with UVM clinicopathological features, which was also an independent predictor for overall survival (OS). Intriguingly, CARD11 had a positively correlation to autophagy, cellular senescence and apoptosis. Infiltration of monocytes was significantly higher in low CARD11 expression group, and infiltration of T cells regulatory was lower in the same group. Functional enrichment analyses revealed that CARD11 was positively related to T cell activation pathways and cell adhesion molecules. The expressions of hub-genes were all increased in the high CARD11 expression group and the ceRNA network showed the interaction among mRNA, miRNA and lncRNA. These findings show that high CARD11 expression in UVM is associated with poor OS, indicating that CARD11 may serve as a potential biomarker for the diagnosis and prognosis of the UVM.
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Our study analyzed prognostic value and immune-related characteristics of CARD11 in UVM, hoping to provide a potential management and research direction. The RNA-sequence data of 80 UVM patients were downloaded from The Cancer Genome Atlas database and divided them into high- and low-expression groups. We analyzed the differentially expressed genes, enrichment analyses and the infiltration of immune cells using the R package and Gene-Set Enrichment Analysis. A clinical prediction nomogram and protein-protein interaction network were constructed and the first 8 genes were considered as the hub-genes. Finally, we constructed a competing endogenous RNA (ceRNA) network by Cytoscape and analyzed the statistical data via the R software. Here we found that CARD11 expression had notable correlation with UVM clinicopathological features, which was also an independent predictor for overall survival (OS). Intriguingly, CARD11 had a positively correlation to autophagy, cellular senescence and apoptosis. Infiltration of monocytes was significantly higher in low CARD11 expression group, and infiltration of T cells regulatory was lower in the same group. Functional enrichment analyses revealed that CARD11 was positively related to T cell activation pathways and cell adhesion molecules. The expressions of hub-genes were all increased in the high CARD11 expression group and the ceRNA network showed the interaction among mRNA, miRNA and lncRNA. These findings show that high CARD11 expression in UVM is associated with poor OS, indicating that CARD11 may serve as a potential biomarker for the diagnosis and prognosis of the UVM.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0255293</identifier><identifier>PMID: 34370778</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Analysis ; Apoptosis ; Autophagy ; Biological markers ; Biology and Life Sciences ; Biomarkers ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Cancer ; CARD Signaling Adaptor Proteins - genetics ; CARD Signaling Adaptor Proteins - metabolism ; Cell activation ; Cell adhesion ; Cell adhesion molecules ; Correlation ; Dermatology ; Enrichment ; Eye diseases ; Female ; Gene expression ; Gene Expression Regulation, Neoplastic ; Gene Regulatory Networks ; Gene set enrichment analysis ; Genes ; Genomes ; Hospitals ; Humans ; Immune system ; Infiltration ; Integrative medicine ; Kinases ; Lymphocytes ; Lymphocytes T ; Lymphoma ; Male ; Malignancy ; Medical laboratories ; Medical prognosis ; Medicine ; Medicine and Health Sciences ; Melanoma ; Melanoma - genetics ; Melanoma - immunology ; Melanoma - mortality ; Melanoma - pathology ; Middle Aged ; miRNA ; Monocytes ; Mortality ; mRNA ; Nomograms ; Nomographs ; Nucleotide sequence ; Phagocytosis ; Prognosis ; Prostate cancer ; Protein interaction ; Protein Interaction Maps ; Proteins ; Ribonucleic acid ; RNA ; Senescence ; Uveal Neoplasms - genetics ; Uveal Neoplasms - immunology ; Uveal Neoplasms - mortality ; Uveal Neoplasms - pathology</subject><ispartof>PloS one, 2021-08, Vol.16 (8), p.e0255293</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Shi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Xueying</au><au>Xia, Shilin</au><au>Chu, Yingming</au><au>Yang, Nan</au><au>Zheng, Jingyuan</au><au>Chen, Qianyi</au><au>Fen, Zeng</au><au>Jiang, Yuankuan</au><au>Fang, Shifeng</au><au>Lin, Jingrong</au><au>Haass, Nikolas K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CARD11 is a prognostic biomarker and correlated with immune infiltrates in uveal melanoma</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2021-08-09</date><risdate>2021</risdate><volume>16</volume><issue>8</issue><spage>e0255293</spage><pages>e0255293-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Uveal melanoma (UVM), the most common primary intraocular malignancy, has a high mortality because of a high propensity to metastasize. Our study analyzed prognostic value and immune-related characteristics of CARD11 in UVM, hoping to provide a potential management and research direction. The RNA-sequence data of 80 UVM patients were downloaded from The Cancer Genome Atlas database and divided them into high- and low-expression groups. We analyzed the differentially expressed genes, enrichment analyses and the infiltration of immune cells using the R package and Gene-Set Enrichment Analysis. A clinical prediction nomogram and protein-protein interaction network were constructed and the first 8 genes were considered as the hub-genes. Finally, we constructed a competing endogenous RNA (ceRNA) network by Cytoscape and analyzed the statistical data via the R software. Here we found that CARD11 expression had notable correlation with UVM clinicopathological features, which was also an independent predictor for overall survival (OS). Intriguingly, CARD11 had a positively correlation to autophagy, cellular senescence and apoptosis. Infiltration of monocytes was significantly higher in low CARD11 expression group, and infiltration of T cells regulatory was lower in the same group. Functional enrichment analyses revealed that CARD11 was positively related to T cell activation pathways and cell adhesion molecules. The expressions of hub-genes were all increased in the high CARD11 expression group and the ceRNA network showed the interaction among mRNA, miRNA and lncRNA. These findings show that high CARD11 expression in UVM is associated with poor OS, indicating that CARD11 may serve as a potential biomarker for the diagnosis and prognosis of the UVM.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>34370778</pmid><doi>10.1371/journal.pone.0255293</doi><tpages>e0255293</tpages><orcidid>https://orcid.org/0000-0002-4737-0856</orcidid><oa>free_for_read</oa></addata></record>
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subjects Analysis
Apoptosis
Autophagy
Biological markers
Biology and Life Sciences
Biomarkers
Biomarkers, Tumor - genetics
Biomarkers, Tumor - metabolism
Cancer
CARD Signaling Adaptor Proteins - genetics
CARD Signaling Adaptor Proteins - metabolism
Cell activation
Cell adhesion
Cell adhesion molecules
Correlation
Dermatology
Enrichment
Eye diseases
Female
Gene expression
Gene Expression Regulation, Neoplastic
Gene Regulatory Networks
Gene set enrichment analysis
Genes
Genomes
Hospitals
Humans
Immune system
Infiltration
Integrative medicine
Kinases
Lymphocytes
Lymphocytes T
Lymphoma
Male
Malignancy
Medical laboratories
Medical prognosis
Medicine
Medicine and Health Sciences
Melanoma
Melanoma - genetics
Melanoma - immunology
Melanoma - mortality
Melanoma - pathology
Middle Aged
miRNA
Monocytes
Mortality
mRNA
Nomograms
Nomographs
Nucleotide sequence
Phagocytosis
Prognosis
Prostate cancer
Protein interaction
Protein Interaction Maps
Proteins
Ribonucleic acid
RNA
Senescence
Uveal Neoplasms - genetics
Uveal Neoplasms - immunology
Uveal Neoplasms - mortality
Uveal Neoplasms - pathology
title CARD11 is a prognostic biomarker and correlated with immune infiltrates in uveal melanoma
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