Evidence map›Paper›PMID 41053452›Full record

ArticleHuman cell2025

Multi-omic analysis constructs ferroptosis subtypes and risk signature and reveals that PEBP1 is an important tumor suppressor in kidney cancer.

Shuaiqi Chen, Xizi Cheng, Zeyu Li, Huijun Fan, Xiangdong Xue, Kuo Ma, Jingxian Li, Feng Zhu

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Article in Human cell, 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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8 authors.

Shuaiqi ChenDepartment of Urology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Xizi ChengDepartment of Urology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Zeyu LiDepartment of Urology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Huijun FanUltrasonography Department, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Xiangdong XueDepartment of Urology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Kuo MaDepartment of Urology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China.
Jingxian LiDepartment of Urology, Tianjin Institute of Urology, The Second Hospital of Tianjin Medical University, Tianjin, China.
Feng ZhuDepartment of Urology, The First Affiliated Hospital of Xinxiang Medical University, Xinxiang, China. zfdmb@163.com.

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6 · The paper itself

Abstract

Ferroptosis, an iron-dependent type of regulated cell death driven by excessive lipid peroxidation, plays an important role in natural tumor suppression. In this study, we identified 23 ferroptosis-related genes associated with prognosis in kidney cancer datasets. Based on the expression profiles of these genes, we classified kidney cancer into four distinct subtypes and constructed a 9-gene risk score to predict the prognosis of patients. Our analysis revealed that patients classified into group III and those in the low-risk group demonstrated significantly better survival probability. Moreover, the risk score exhibited strong predictive accuracy for the prognosis of kidney renal clear-cell carcinoma (KIRC) patients. Among the identified genes, PEBP1 showed elevated expression in both subtype III and the low-risk group, suggesting that it may act as a critical tumor suppressor. To further evaluate this, we examined PEBP1 expression patterns and their clinical correlations using TCGA-KIRC and KIRP cohorts. The results indicated that PEBP1 deletion was strongly associated with poor prognosis, while reduced PEBP1 expression correlated with advanced disease progression in both KIRC and KIRP patients. Functional enrichment analysis suggested that PEBP1 may be involved in pathways related to fatty acid metabolism and oxidative phosphorylation. Experimental validation supported these findings, showing that PEBP1 overexpression suppressed the proliferation and migration of kidney cancer cells. Additionally, PEBP1 promoted the accumulation of lipid reactive oxygen species (ROS), an effect that was reversed by a ferroptosis inhibitor. Conversely, silencing PEBP1 counteracted the lipid ROS induced by RSL4, a ferroptosis activator. In summary, our results demonstrate that PEBP1 functions as a potential tumor suppressor in kidney cancer and may serve as a promising prognostic biomarker and therapeutic target.

Indexed as

Carcinoma, Renal CellFerroptosisGenes, Tumor SuppressorKidney NeoplasmsPhosphatidylethanolamine Binding ProteinCell ProliferationHumansMultiomicsPrognosisPhosphatidylethanolamine Binding ProteinFatty acid metabolismFerroptosisKIRCKIRPPEBP1

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.