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A novel gene signature related to oxidative stress predicts the prognosis in clear cell renal cell carcinoma
Clear cell renal cell carcinoma (ccRCC) is considered to be related to the worse prognosis, which might in part be attributed to the early recurrence and metastasis, compared with other type of kidney cancer. Oxidative stress refers to an imbalance between production of oxidants and antioxidant defe...
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Published in: | PeerJ (San Francisco, CA) CA), 2023-02, Vol.11, p.e14784-e14784, Article e14784 |
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description | Clear cell renal cell carcinoma (ccRCC) is considered to be related to the worse prognosis, which might in part be attributed to the early recurrence and metastasis, compared with other type of kidney cancer. Oxidative stress refers to an imbalance between production of oxidants and antioxidant defense. Accumulative studies have indicated that oxidative stress genes contribute to the tumor invasion, metastasis and drug sensitivity. However, the biological functions of oxidative stress genes in ccRCC remain largely unknown. In this study, we identified 1,399 oxidative stress genes from GeneCards with a relevance score ≥7. Data for analysis were accessed from The Cancer Genome Atlas (TCGA) and the International Cancer Genome Consortium (ICGC) database, and were utilized as training set and validation set respectively. Univariate Cox analysis, least absolute shrinkage and selection operator (LASSO) Cox regression and multivariate Cox were employed to construct a prognostic signature in ccRCC. Finally, a prognostic signature including four different oxidative stress genes was constructed from 1,399 genes, and its predictive performance was verified through Kaplan-Meier survival analysis and the receiver operating characteristic (ROC) curve. Interestingly, we found that there was significant correlation between the expression of oxidative stress genes and the immune infiltration and the sensitivity of tumor cells to chemotherapeutics. Moreover, the highest hazard ratio gene urocortin (
) was chosen for further study; some necessary vitro experiments proved that the
could promote the ability of ccRCC proliferation and migration and contribute to the degree of oxidative stress. In conclusion, it was promising to predict the prognosis of ccRCC through the four oxidative stress genes signature.
played oncogenic roles in ccRCC by influencing proliferation and oxidative stress pathway, which was expected to be the novel therapeutic target for ccRCC. |
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) was chosen for further study; some necessary vitro experiments proved that the
could promote the ability of ccRCC proliferation and migration and contribute to the degree of oxidative stress. In conclusion, it was promising to predict the prognosis of ccRCC through the four oxidative stress genes signature.
played oncogenic roles in ccRCC by influencing proliferation and oxidative stress pathway, which was expected to be the novel therapeutic target for ccRCC.</description><identifier>ISSN: 2167-8359</identifier><identifier>EISSN: 2167-8359</identifier><identifier>DOI: 10.7717/peerj.14784</identifier><identifier>PMID: 36785707</identifier><language>eng</language><publisher>United States: PeerJ. Ltd</publisher><subject>Bioinformatics ; Biomarker ; Cancer ; Carcinoma ; Carcinoma, Renal cell ; Carcinoma, Renal Cell - genetics ; Cell Biology ; Cell growth ; Clear cell renal cell carcinoma ; Clear cell-type renal cell carcinoma ; Cluster analysis ; Comparative analysis ; Gene expression ; Genes ; Genetic aspects ; Genomes ; Genomics ; Health aspects ; Humans ; Kidney cancer ; Kidney Neoplasms - genetics ; Medical Genetics ; Medical prognosis ; Metastases ; Mutation ; Oncology ; Oxidants ; Oxidative stress ; Oxidative Stress - genetics ; Plasmids ; Prognosis ; Therapeutic targets ; Tumor cells ; UCN ; Urocortin ; Urology</subject><ispartof>PeerJ (San Francisco, CA), 2023-02, Vol.11, p.e14784-e14784, Article e14784</ispartof><rights>2023 Ma et al.</rights><rights>COPYRIGHT 2023 PeerJ. Ltd.</rights><rights>2023 Ma et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 Ma et al. 2023 Ma et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c573t-de650e3275bc5e9fd757a0a048bc90f22098f17e4791a3022f9385ef6537dc423</citedby><cites>FETCH-LOGICAL-c573t-de650e3275bc5e9fd757a0a048bc90f22098f17e4791a3022f9385ef6537dc423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2774348507/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2774348507?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36785707$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ma, Sheng</creatorcontrib><creatorcontrib>Ge, Yue</creatorcontrib><creatorcontrib>Xiong, Zezhong</creatorcontrib><creatorcontrib>Wang, Yanan</creatorcontrib><creatorcontrib>Li, Le</creatorcontrib><creatorcontrib>Chao, Zheng</creatorcontrib><creatorcontrib>Li, Beining</creatorcontrib><creatorcontrib>Zhang, Junbiao</creatorcontrib><creatorcontrib>Ma, Siquan</creatorcontrib><creatorcontrib>Xiao, Jun</creatorcontrib><creatorcontrib>Liu, Bo</creatorcontrib><creatorcontrib>Wang, Zhihua</creatorcontrib><title>A novel gene signature related to oxidative stress predicts the prognosis in clear cell renal cell carcinoma</title><title>PeerJ (San Francisco, CA)</title><addtitle>PeerJ</addtitle><description>Clear cell renal cell carcinoma (ccRCC) is considered to be related to the worse prognosis, which might in part be attributed to the early recurrence and metastasis, compared with other type of kidney cancer. Oxidative stress refers to an imbalance between production of oxidants and antioxidant defense. Accumulative studies have indicated that oxidative stress genes contribute to the tumor invasion, metastasis and drug sensitivity. However, the biological functions of oxidative stress genes in ccRCC remain largely unknown. In this study, we identified 1,399 oxidative stress genes from GeneCards with a relevance score ≥7. Data for analysis were accessed from The Cancer Genome Atlas (TCGA) and the International Cancer Genome Consortium (ICGC) database, and were utilized as training set and validation set respectively. Univariate Cox analysis, least absolute shrinkage and selection operator (LASSO) Cox regression and multivariate Cox were employed to construct a prognostic signature in ccRCC. Finally, a prognostic signature including four different oxidative stress genes was constructed from 1,399 genes, and its predictive performance was verified through Kaplan-Meier survival analysis and the receiver operating characteristic (ROC) curve. Interestingly, we found that there was significant correlation between the expression of oxidative stress genes and the immune infiltration and the sensitivity of tumor cells to chemotherapeutics. Moreover, the highest hazard ratio gene urocortin (
) was chosen for further study; some necessary vitro experiments proved that the
could promote the ability of ccRCC proliferation and migration and contribute to the degree of oxidative stress. In conclusion, it was promising to predict the prognosis of ccRCC through the four oxidative stress genes signature.
played oncogenic roles in ccRCC by influencing proliferation and oxidative stress pathway, which was expected to be the novel therapeutic target for ccRCC.</description><subject>Bioinformatics</subject><subject>Biomarker</subject><subject>Cancer</subject><subject>Carcinoma</subject><subject>Carcinoma, Renal cell</subject><subject>Carcinoma, Renal Cell - genetics</subject><subject>Cell Biology</subject><subject>Cell growth</subject><subject>Clear cell renal cell carcinoma</subject><subject>Clear cell-type renal cell carcinoma</subject><subject>Cluster analysis</subject><subject>Comparative analysis</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genomes</subject><subject>Genomics</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Kidney cancer</subject><subject>Kidney Neoplasms - genetics</subject><subject>Medical Genetics</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Mutation</subject><subject>Oncology</subject><subject>Oxidants</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - genetics</subject><subject>Plasmids</subject><subject>Prognosis</subject><subject>Therapeutic targets</subject><subject>Tumor cells</subject><subject>UCN</subject><subject>Urocortin</subject><subject>Urology</subject><issn>2167-8359</issn><issn>2167-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkluLEzEUgAdR3GXdJ98lIIggXTO5TJIXoSxeFhZ80eeQyZxMU6ZJTTJF_71pu66tmDzk9p0vyeE0zcsW3wjRivdbgLS-aZmQ7ElzSdpOLCTl6unJ_KK5znmNa5Okw5I-by5oJyQXWFw20xKFuIMJjRAAZT8GU-YEKMFkCgyoRBR_-sEUv6vHJUHOaJtg8LZkVFZQF3EMMfuMfEB2ApOQhWmqgmCm49SaZH2IG_OieebMlOH6Ybxqvn_6-O32y-L-6-e72-X9wnJBy2KAjmOgRPDeclBuEFwYbDCTvVXYEYKVdK0AJlRrKCbEKSo5uI5TMVhG6FVzd_QO0az1NvmNSb90NF4fNmIatUnF19dq6wyVjCtqe2Ccs54zx50wQ--MEqqvrg9H13buNzBYCCWZ6Ux6fhL8So9xp5UirZKyCt4-CFL8MUMueuPzPi8mQJyzJkJ0vK0v4BV9_Q-6jnOqeTxQjDLJsfhLjaZ-wAcX6712L9VLQTtCW4H3rpv_ULUPsPE2BnC-7p8FvDkJWIGZyirHaS4-hnwOvjuCNsWcE7jHZLRY74tSH4pSH4qy0q9O8_fI_ilB-hv8PtyN</recordid><startdate>20230208</startdate><enddate>20230208</enddate><creator>Ma, Sheng</creator><creator>Ge, Yue</creator><creator>Xiong, Zezhong</creator><creator>Wang, Yanan</creator><creator>Li, Le</creator><creator>Chao, Zheng</creator><creator>Li, Beining</creator><creator>Zhang, Junbiao</creator><creator>Ma, Siquan</creator><creator>Xiao, Jun</creator><creator>Liu, Bo</creator><creator>Wang, Zhihua</creator><general>PeerJ. 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Oxidative stress refers to an imbalance between production of oxidants and antioxidant defense. Accumulative studies have indicated that oxidative stress genes contribute to the tumor invasion, metastasis and drug sensitivity. However, the biological functions of oxidative stress genes in ccRCC remain largely unknown. In this study, we identified 1,399 oxidative stress genes from GeneCards with a relevance score ≥7. Data for analysis were accessed from The Cancer Genome Atlas (TCGA) and the International Cancer Genome Consortium (ICGC) database, and were utilized as training set and validation set respectively. Univariate Cox analysis, least absolute shrinkage and selection operator (LASSO) Cox regression and multivariate Cox were employed to construct a prognostic signature in ccRCC. Finally, a prognostic signature including four different oxidative stress genes was constructed from 1,399 genes, and its predictive performance was verified through Kaplan-Meier survival analysis and the receiver operating characteristic (ROC) curve. Interestingly, we found that there was significant correlation between the expression of oxidative stress genes and the immune infiltration and the sensitivity of tumor cells to chemotherapeutics. Moreover, the highest hazard ratio gene urocortin (
) was chosen for further study; some necessary vitro experiments proved that the
could promote the ability of ccRCC proliferation and migration and contribute to the degree of oxidative stress. In conclusion, it was promising to predict the prognosis of ccRCC through the four oxidative stress genes signature.
played oncogenic roles in ccRCC by influencing proliferation and oxidative stress pathway, which was expected to be the novel therapeutic target for ccRCC.</abstract><cop>United States</cop><pub>PeerJ. Ltd</pub><pmid>36785707</pmid><doi>10.7717/peerj.14784</doi><oa>free_for_read</oa></addata></record> |
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subjects | Bioinformatics Biomarker Cancer Carcinoma Carcinoma, Renal cell Carcinoma, Renal Cell - genetics Cell Biology Cell growth Clear cell renal cell carcinoma Clear cell-type renal cell carcinoma Cluster analysis Comparative analysis Gene expression Genes Genetic aspects Genomes Genomics Health aspects Humans Kidney cancer Kidney Neoplasms - genetics Medical Genetics Medical prognosis Metastases Mutation Oncology Oxidants Oxidative stress Oxidative Stress - genetics Plasmids Prognosis Therapeutic targets Tumor cells UCN Urocortin Urology |
title | A novel gene signature related to oxidative stress predicts the prognosis in clear cell renal cell carcinoma |
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