Bioinformatics Analysis of Autophagy-Related Genes in Kidney Transplantation.

IF 0.8 4区 医学 Q4 UROLOGY & NEPHROLOGY
Cankun Xie, Wingkeung Yiu, Jiahui Jie, Yonglu Wu, Guanjun Li
{"title":"Bioinformatics Analysis of Autophagy-Related Genes in Kidney Transplantation.","authors":"Cankun Xie, Wingkeung Yiu, Jiahui Jie, Yonglu Wu, Guanjun Li","doi":"10.52547/c9btn873","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Autophagy related genes (ARGs) may play important roles in various biological processes involving kidney transplantation (KT); however, their expression characteristics are rarely used to study the relationship between autophagy and prognosis in KT patients. This study aims to construct a new autophagy related gene feature based on high-throughput sequencing datasets.</p><p><strong>Methods: </strong>Differentially expressed ARGs (DEARGs) were identified in KT patients based on the Gene Expression Omnibus (GEO) database. Gene Ontology (GO)and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed to explore potential biological and pathological functions of DEARGs. Univariate and Lasso Cox regression analyses identified survival-related DEARGs and established a prognostic gene signature whose performance was evaluated by Kaplan-Meier curve and receiver operating characteristic (ROC). Moreover, the prognostic value of the gene signature was further validated in 48 KT patients from the GSE21374 dataset.  Results. A total of 28 common DEARGs were identified between rejection and non-rejection samples in 3 datasets, including GSE21374, GSE36059, and GSE48581. GO and KEGG enrichment analyses showed that DEARGs were mainly involved in regulating apoptotic processes. In addition, we identified and validated 7 DEARGs (CASP1, CASP3, FKBP1A, RAB11A, NFKB1, RGS19, and CCL2) as the prognostic signatures. The Kaplan-Meier (K-M) analysis showed that the survival rate of the high-risk patients was significantly lower than that of the low-risk patients.</p><p><strong>Conclusion: </strong>The effectiveness of autophagy related features was validated by using 48 KT patients in the GSE21374 dataset, and establishing and confirming a new ARG signal with independent survival prognostic value for KT patients.</p>","PeriodicalId":14610,"journal":{"name":"Iranian journal of kidney diseases","volume":"18 6","pages":"337-359"},"PeriodicalIF":0.8000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian journal of kidney diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.52547/c9btn873","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"UROLOGY & NEPHROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Autophagy related genes (ARGs) may play important roles in various biological processes involving kidney transplantation (KT); however, their expression characteristics are rarely used to study the relationship between autophagy and prognosis in KT patients. This study aims to construct a new autophagy related gene feature based on high-throughput sequencing datasets.

Methods: Differentially expressed ARGs (DEARGs) were identified in KT patients based on the Gene Expression Omnibus (GEO) database. Gene Ontology (GO)and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were performed to explore potential biological and pathological functions of DEARGs. Univariate and Lasso Cox regression analyses identified survival-related DEARGs and established a prognostic gene signature whose performance was evaluated by Kaplan-Meier curve and receiver operating characteristic (ROC). Moreover, the prognostic value of the gene signature was further validated in 48 KT patients from the GSE21374 dataset.  Results. A total of 28 common DEARGs were identified between rejection and non-rejection samples in 3 datasets, including GSE21374, GSE36059, and GSE48581. GO and KEGG enrichment analyses showed that DEARGs were mainly involved in regulating apoptotic processes. In addition, we identified and validated 7 DEARGs (CASP1, CASP3, FKBP1A, RAB11A, NFKB1, RGS19, and CCL2) as the prognostic signatures. The Kaplan-Meier (K-M) analysis showed that the survival rate of the high-risk patients was significantly lower than that of the low-risk patients.

Conclusion: The effectiveness of autophagy related features was validated by using 48 KT patients in the GSE21374 dataset, and establishing and confirming a new ARG signal with independent survival prognostic value for KT patients.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Iranian journal of kidney diseases
Iranian journal of kidney diseases UROLOGY & NEPHROLOGY-
CiteScore
2.50
自引率
0.00%
发文量
43
审稿时长
6-12 weeks
期刊介绍: The Iranian Journal of Kidney Diseases (IJKD), a peer-reviewed journal in English, is the official publication of the Iranian Society of Nephrology. The aim of the IJKD is the worldwide reflection of the knowledge produced by the scientists and clinicians in nephrology. Published quarterly, the IJKD provides a new platform for advancement of the field. The journal’s objective is to serve as a focal point for debates and exchange of knowledge and experience among researchers in a global context. Original papers, case reports, and invited reviews on all aspects of the kidney diseases, hypertension, dialysis, and transplantation will be covered by the IJKD. Research on the basic science, clinical practice, and socio-economics of renal health are all welcomed by the editors of the journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信