Evidence map›Paper›PMID 33650306›Full record

ArticleCancer medicine2021

Construction and validation of an autophagy-related long noncoding RNA signature for prognosis prediction in kidney renal clear cell carcinoma patients.

JunJie Yu, WeiPu Mao, Bin Xu, Ming Chen

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Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

JunJie YuDepartment of medical college, Southeast University, Nanjing, China.ORCID 0000-0001-8920-7064
WeiPu MaoDepartment of medical college, Southeast University, Nanjing, China.
Bin XuDepartment of Urology, Southeast University Zhongda hospital, Nanjing, China.
Ming ChenDepartment of Urology, Southeast University Zhongda hospital, Nanjing, China.ORCID 0000-0002-3572-6886

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe purpose of this study was to identify autophagy-associated long noncoding RNAs (ARlncRNAs) using the kidney renal clear cell carcinoma (KIRC) patient data from The Cancer Genome Atlas (TCGA) database and to construct a prognostic risk-related ARlncRNAs signature to accurately predict the prognosis of KIRC patients.

methodsThe KIRC patient data were originated from TCGA database and were classified into a training set and testing set. Seven prognostic risk-related ARlncRNAs, identified using univariate, lasso, and multivariate Cox regression analysis, were used to construct prognostic risk-related signatures. Kaplan-Meier curves and receiver operating characteristic (ROC) curves as well as independent prognostic factor analysis and correlation analysis with clinical characteristics were utilized to evaluate and verify the specificity and sensitivity of the signature in training set and testing set, respectively. Two nomograms were established to predict the probable 1-, 3-, and 5-year survival of the KIRC patients. In addition, the lncRNA-mRNA co-expression network was constructed and Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to identify biological functions of ARlncRNAs.

resultsWe constructed and verified a prognostic risk-related ARlncRNAs signature in training set and testing set, respectively. We found the survival time of KIRC patients with low-risk scores was significantly better than those with high-risk scores in training set and testing set. ROC curves suggested that the area under the ROC (AUC) value for prognostic risk score signature was 0.81 in training set and 0.705 in testing set. And AUC values corresponding to 1-, 3-, and 5 years of OS were 0.809, 0.753, and 0.794 in training set and 0.698, 0.682, and 0.754 in testing set, respectively. We established the two nomograms that confirmed high C-index and accomplished good prediction accuracy.

conclusionsWe constructed a prognostic risk-related ARlncRNAs signature that could accurately predict the prognosis of KIRC patients.

Indexed as

TranscriptomeArea Under CurveAutophagyCarcinoma, Renal CellDatabases, GeneticHumansKaplan-Meier EstimateKidney NeoplasmsNomogramsProportional Hazards ModelsRiskRisk FactorsRNA, Long NoncodingRNA, MessengerROC CurveSensitivity and SpecificityRNA, Long NoncodingRNA, Messengerautophagykidney renal clear cell carcinomalong noncoding RNAprognostic signatureThe Cancer Genome Atlas

Identifiers

PMID33650306
PMCPMC7982638

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.