Evidence map›Paper›PMID 40853971›Full record

ArticlePLoS computational biology2025

Integrated pan-cancer analysis of RNA binding protein HuR investigates its biomarker potential in prognosis, immunotherapy, and drug sensitivity.

Jian Peng, Jichuan Quan, Xiaoru Wang

Abstract read
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Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jian PengAnhui Institute of Pediatric Research, Anhui Provincial Children's Hospital, Hefei, Anhui, China.ORCID 0009-0009-6780-4330
Jichuan QuanDepartment of Colorectal Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Xiaoru WangDepartment of Critical Care Medicine, Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.

Funding

Research Project of Health Commission of Shanxi Province
6 · The paper itself

Abstract

backgroundWhile the RNA-binding protein HuR is implicated in individual cancers, its comprehensive diagnostic, prognostic, and immunological roles across diverse cancer types remain unexplored.

methodsWe performed an integrated pan-cancer analysis of HuR using public datasets. This encompassed expression profiling, survival analysis, diagnostic accuracy assessment, immune microenvironment characterization, and drug sensitivity prediction. We investigated HuR's regulatory mechanisms through pathway correlation and differential gene expression analyses.

resultsHuR expression was consistently elevated across multiple cancers and correlated with poor patient prognosis. It demonstrated high diagnostic accuracy (>85%) via TMB/PD-L1 biomarkers. High HuR expression was associated with an immunosuppressive tumor microenvironment and reduced efficacy of immune checkpoint inhibitors, establishing it as a key immunoregulatory biomarker. HuR also predicted sensitivity to cell cycle inhibitors and other pathway-targeted drugs. Mechanistically, HuR drives malignancy by dysregulating core processes: cell cycle progression, immune evasion, and cellular metabolism.

conclusionsOur pan-cancer analysis establishes HuR as a consistently upregulated oncogenic driver across malignancies, functioning as a potential universal biomarker for prognosis and diagnosis. Its critical roles in modulating the immune response and predicting therapeutic sensitivity highlight its importance for personalized cancer treatment strategies. HuR orchestrates tumorigenesis and malignant progression by integrally regulating vital cellular processes.

Indexed as

Biomarkers, TumorELAV-Like Protein 1NeoplasmsComputational BiologyGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunotherapyPrognosisTumor MicroenvironmentBiomarkers, TumorELAVL1 protein, humanELAV-Like Protein 1

Identifiers

PMID40853971
PMCPMC12377624

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