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The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation

BACKGROUND: This study aims to identify potential biomarkers associated with acute kidney injury (AKI) post kidney transplantation. MATERIAL AND METHODS: Two mRNA expression profiles from Gene Expression Omnibus repertory were downloaded, including 20 delayed graft function (DGF) and 68 immediate gr...

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Autores principales: Bi, Hui, Zhang, Min, Wang, Jialin, Long, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703406/
https://www.ncbi.nlm.nih.gov/pubmed/33312771
http://dx.doi.org/10.7717/peerj.10441
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author Bi, Hui
Zhang, Min
Wang, Jialin
Long, Gang
author_facet Bi, Hui
Zhang, Min
Wang, Jialin
Long, Gang
author_sort Bi, Hui
collection PubMed
description BACKGROUND: This study aims to identify potential biomarkers associated with acute kidney injury (AKI) post kidney transplantation. MATERIAL AND METHODS: Two mRNA expression profiles from Gene Expression Omnibus repertory were downloaded, including 20 delayed graft function (DGF) and 68 immediate graft function (IGF) samples. Differentially expressed genes (DEGs) were identified between DGF and IGF group. The Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis of DEGs were performed. Then, a protein-protein interaction analysis was performed to extract hub genes. The key genes were searched by literature retrieval and cross-validated based on the training dataset. An external dataset was used to validate the expression levels of key genes. Receiver operating characteristic curve analyses were performed to evaluate diagnostic performance of key genes for AKI. RESULTS: A total of 330 DEGs were identified between DGF and IGF samples, including 179 up-regulated and 151 down-regulated genes. Of these, OLIG3, EBF3 and ETV1 were transcription factor genes. Moreover, LEP, EIF4A3, WDR3, MC4R, PPP2CB, DDX21 and GPT served as hub genes in PPI network. EBF3 was significantly up-regulated in validation GSE139061 dataset, which was consistently with our initial gene differential expression analysis. Finally, we found that LEP had a great diagnostic value for AKI (AUC = 0.740). CONCLUSION: EBF3 may be associated with the development of AKI following kidney transplantation. Furthermore, LEP had a good diagnostic value for AKI. These findings provide deeper insights into the diagnosis and management of AKI post renal transplantation.
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spelling pubmed-77034062020-12-10 The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation Bi, Hui Zhang, Min Wang, Jialin Long, Gang PeerJ Bioinformatics BACKGROUND: This study aims to identify potential biomarkers associated with acute kidney injury (AKI) post kidney transplantation. MATERIAL AND METHODS: Two mRNA expression profiles from Gene Expression Omnibus repertory were downloaded, including 20 delayed graft function (DGF) and 68 immediate graft function (IGF) samples. Differentially expressed genes (DEGs) were identified between DGF and IGF group. The Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analysis of DEGs were performed. Then, a protein-protein interaction analysis was performed to extract hub genes. The key genes were searched by literature retrieval and cross-validated based on the training dataset. An external dataset was used to validate the expression levels of key genes. Receiver operating characteristic curve analyses were performed to evaluate diagnostic performance of key genes for AKI. RESULTS: A total of 330 DEGs were identified between DGF and IGF samples, including 179 up-regulated and 151 down-regulated genes. Of these, OLIG3, EBF3 and ETV1 were transcription factor genes. Moreover, LEP, EIF4A3, WDR3, MC4R, PPP2CB, DDX21 and GPT served as hub genes in PPI network. EBF3 was significantly up-regulated in validation GSE139061 dataset, which was consistently with our initial gene differential expression analysis. Finally, we found that LEP had a great diagnostic value for AKI (AUC = 0.740). CONCLUSION: EBF3 may be associated with the development of AKI following kidney transplantation. Furthermore, LEP had a good diagnostic value for AKI. These findings provide deeper insights into the diagnosis and management of AKI post renal transplantation. PeerJ Inc. 2020-11-27 /pmc/articles/PMC7703406/ /pubmed/33312771 http://dx.doi.org/10.7717/peerj.10441 Text en ©2020 Bi et al. https://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by-nc/4.0) , which permits using, remixing, and building upon the work non-commercially, as long as 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.
spellingShingle Bioinformatics
Bi, Hui
Zhang, Min
Wang, Jialin
Long, Gang
The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation
title The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation
title_full The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation
title_fullStr The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation
title_full_unstemmed The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation
title_short The mRNA landscape profiling reveals potential biomarkers associated with acute kidney injury AKI after kidney transplantation
title_sort mrna landscape profiling reveals potential biomarkers associated with acute kidney injury aki after kidney transplantation
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703406/
https://www.ncbi.nlm.nih.gov/pubmed/33312771
http://dx.doi.org/10.7717/peerj.10441
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