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Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis

Kidney transplantation is the promising treatment of choice for chronic kidney disease and end-stage kidney disease and can effectively improve the quality of life and survival rates of patients. However, the allograft rejection following kidney transplantation has a negative impact on transplant su...

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Autores principales: Wang, Li-Jun, Ma, Xiao-Bo, Xia, Hong-Ying, Sun, Xun, Yu, Lu, Yang, Qian, Hu, Zong-Qiang, Zhao, Yong-Heng, Hu, Wei, Ran, Jiang-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342162/
https://www.ncbi.nlm.nih.gov/pubmed/34368360
http://dx.doi.org/10.1155/2021/9933136
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author Wang, Li-Jun
Ma, Xiao-Bo
Xia, Hong-Ying
Sun, Xun
Yu, Lu
Yang, Qian
Hu, Zong-Qiang
Zhao, Yong-Heng
Hu, Wei
Ran, Jiang-Hua
author_facet Wang, Li-Jun
Ma, Xiao-Bo
Xia, Hong-Ying
Sun, Xun
Yu, Lu
Yang, Qian
Hu, Zong-Qiang
Zhao, Yong-Heng
Hu, Wei
Ran, Jiang-Hua
author_sort Wang, Li-Jun
collection PubMed
description Kidney transplantation is the promising treatment of choice for chronic kidney disease and end-stage kidney disease and can effectively improve the quality of life and survival rates of patients. However, the allograft rejection following kidney transplantation has a negative impact on transplant success. Therefore, the present study is aimed at screening novel biomarkers for the diagnosis and treatment of allograft rejection following kidney transplantation for improving long-term transplant outcome. In the study, a total of 8 modules and 3065 genes were identified by WGCNA based on the GSE46474 and GSE15296 dataset from the Gene Expression Omnibus (GEO) database. Moreover, the results of Gene Ontology (GO) annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis showed that these genes were mainly involved in the immune-related biological processes and pathways. Thus, 317 immune-related genes were selected for further analysis. Finally, 5 genes (including CD200R1, VAV2, FASLG, SH2D1B, and RAP2B) were identified as the candidate biomarkers based on the ROC and difference analysis. Furthermore, we also found that in the 5 biomarkers an interaction might exist among each other in the protein and transcription level. Taken together, our study identified CD200R1, VAV2, FASLG, SH2D1B, and RAP2B as the candidate diagnostic biomarkers, which might contribute to the prevention and treatment of allograft rejection following kidney transplantation.
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spelling pubmed-83421622021-08-06 Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis Wang, Li-Jun Ma, Xiao-Bo Xia, Hong-Ying Sun, Xun Yu, Lu Yang, Qian Hu, Zong-Qiang Zhao, Yong-Heng Hu, Wei Ran, Jiang-Hua Biomed Res Int Research Article Kidney transplantation is the promising treatment of choice for chronic kidney disease and end-stage kidney disease and can effectively improve the quality of life and survival rates of patients. However, the allograft rejection following kidney transplantation has a negative impact on transplant success. Therefore, the present study is aimed at screening novel biomarkers for the diagnosis and treatment of allograft rejection following kidney transplantation for improving long-term transplant outcome. In the study, a total of 8 modules and 3065 genes were identified by WGCNA based on the GSE46474 and GSE15296 dataset from the Gene Expression Omnibus (GEO) database. Moreover, the results of Gene Ontology (GO) annotation and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis showed that these genes were mainly involved in the immune-related biological processes and pathways. Thus, 317 immune-related genes were selected for further analysis. Finally, 5 genes (including CD200R1, VAV2, FASLG, SH2D1B, and RAP2B) were identified as the candidate biomarkers based on the ROC and difference analysis. Furthermore, we also found that in the 5 biomarkers an interaction might exist among each other in the protein and transcription level. Taken together, our study identified CD200R1, VAV2, FASLG, SH2D1B, and RAP2B as the candidate diagnostic biomarkers, which might contribute to the prevention and treatment of allograft rejection following kidney transplantation. Hindawi 2021-07-29 /pmc/articles/PMC8342162/ /pubmed/34368360 http://dx.doi.org/10.1155/2021/9933136 Text en Copyright © 2021 Li-Jun Wang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Li-Jun
Ma, Xiao-Bo
Xia, Hong-Ying
Sun, Xun
Yu, Lu
Yang, Qian
Hu, Zong-Qiang
Zhao, Yong-Heng
Hu, Wei
Ran, Jiang-Hua
Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis
title Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis
title_full Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis
title_fullStr Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis
title_full_unstemmed Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis
title_short Identification of Biomarkers for Predicting Allograft Rejection following Kidney Transplantation Based on the Weighted Gene Coexpression Network Analysis
title_sort identification of biomarkers for predicting allograft rejection following kidney transplantation based on the weighted gene coexpression network analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342162/
https://www.ncbi.nlm.nih.gov/pubmed/34368360
http://dx.doi.org/10.1155/2021/9933136
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