Evidence map›Paper›PMID 40530147›Full record

ArticleTranslational cancer research2025

Development and validation of prognostic models based on cell cycle-related signatures for predicting the prognosis of patients with lung adenocarcinoma.

Yuanping Huang, Yanfei Zhao, Yinghui Guan

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Article in Translational cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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3 authors.

Yuanping HuangDepartment of Respiratory Medicine, First Hospital of Jilin University, Changchun, China.
Yanfei ZhaoDepartment of Pediatrics, First Hospital of Jilin University, Changchun, China.
Yinghui GuanDepartment of Respiratory Medicine, First Hospital of Jilin University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lung adenocarcinoma (LUAD) represents the most prevalent histological subtype within lung cancer. Nevertheless, the risk of postoperative metastasis and recurrence remains a substantial concern. We aimed to build the cell cycle-related competing endogenous RNA (ceRNA) networks and potential prognosis prediction models of LUAD, which might provide a valuable reference for studying the prognosis of LUAD. Methods: The RNA sequencing data of LUAD were procured from The Cancer Genome Atlas (TCGA) database and the differentially expressed RNAs were identified from the Ensembl genome browser 96 database [P<0.05 and |log2 fold change (FC)| >1]. The gene expression profile data were acquired from the Gene Expression Omnibus (GEO) repository. A gene set variation analysis was carried out to determine the differentially expressed genes (DEGs) (P<0.05) and a cell cycle-related ceRNA network of LUAD was constructed based on the DEGs. Least absolute shrinkage and selection operator (LASSO) analysis was conducted to acquire the optimized gene combination, a risk score (RS) prognostic risk prediction model was generated subsequently, and a Kaplan-Meier curve was developed to evaluate the efficacy of the RS model. Moreover, we constructed the 3- and 5-year prognostic models of nomogram using R3.6.1 "rms" package, the C-index was counted for accessing predictive capacity. Receiver operating characteristic (ROC) curves were used to evaluate the multiple prognostic risk prediction model. Results: In total, we identified 240 DEGs and constructed the cell cycle-related ceRNA network of LUAD from datasets GSE50081 and GSE37745. Six optimal genes ( Conclusions: This research identified six prognostic biomarkers and built the prognostic prediction models of LUAD, which may enhance the comprehension of disease biology, serve as an effective prognostic tool for LUAD and drive novel therapy development potentially.

Indexed as

competing endogenous RNA regulation network (ceRNA regulation network)Lung adenocarcinoma (LUAD)prognostic prediction model

Identifiers

PMID40530147
PMCPMC12170059

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