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Identification of a prognosis-related gene signature and ceRNA regulatory networks in lung adenocarcinoma

Authors :
Hong Wei
Fei Teng
XiaoLei Wang
XiuJuan Hou
HongBo Wang
Hong Wang
Hui Sun
XianLi Zhou
Source :
Heliyon, Vol 10, Iss 7, Pp e28084- (2024)
Publication Year :
2024
Publisher :
Elsevier, 2024.

Abstract

The ceRNA network, consisting of both noncoding RNA and protein-coding RNA, governs the occurrence, progression, metastasis, and infiltration of lung adenocarcinoma. Signatures comprising multiple genes can effectively determine survival stratification and prognosis of patients with lung adenocarcinoma. To explore the mechanisms of lung adenocarcinoma progression and identify potential biological targets, we carried out systematic bioinformatics analyses of the genetic profiles of lung adenocarcinoma, such as weighted gene co-expression network analysis (WGCNA), differential expression (DE) assessment, univariate and multivariate Cox proportional hazard regression models, ceRNA modulatory networks generated using the ENCORI and miRcode databases, nomogram models, ROC curve assessment, and Kaplan-Meier survival curve analysis. The ceRNA network encompassed 37 nodes, comprising 12 mRNAs, 22 lncRNAs, and three miRNAs. Simultaneously, we performed integration analysis using the 12 genes from the ceRNA network. Our findings revealed that the signature established by these 12 genes serves as an adverse element in lung adenocarcinoma, contributing to unfavorable patient prognosis. To ensure the credibility of our results, we used in vitro experiments for further verification. In conclusion, our study delved into the potential mechanisms underlying lung adenocarcinoma via the ceRNA regulatory network, specifically focusing on the PIF1 and has-miR-125a-5p axis. Additionally, a signature comprising 12 genes was identified as a biomarker related to the prognosis of lung adenocarcinoma.

Details

Language :
English
ISSN :
24058440
Volume :
10
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Heliyon
Publication Type :
Academic Journal
Accession number :
edsdoj.186128d4352d4edba347a95d9f71bf6a
Document Type :
article
Full Text :
https://doi.org/10.1016/j.heliyon.2024.e28084