Evidence map›Paper›PMID 42864662›Full record

ArticleJournal of translational medicine2026

The role of IFNLR1 in modulating T cell infiltration and cancer progression in renal cell carcinoma.

Yawen Zheng, Yufeng Wang, Mingyan Zhang, Mengmeng Zhao, Xinchao Zhao, Feifei Cao, Meili Sun

Abstract read
In one paragraph

Article in Journal of translational medicine, 2026. 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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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yawen ZhengDepartment of Oncology, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250013, P.R. China.
Yufeng Wang
Mingyan ZhangDepartment of Oncology, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250013, P.R. China.
Mengmeng ZhaoResearch Center for Translational Medicine, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250013, P.R. China.
Xinchao ZhaoDepartment of Oncology, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250013, P.R. China.
Feifei CaoDepartment of Oncology, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250013, P.R. China.
Meili SunDepartment of Oncology, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, 250013, P.R. China. smli1980@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundClear cell renal cell carcinoma (ccRCC) is the most common type of kidney cancer, but reliable biomarkers for prognosis and immunotherapy response are lacking.

methodsWe analyzed type III interferon (IFN-λ) and its receptor IFNLR1 expression in ccRCC versus normal tissues using TCGA and GEO datasets, with IFNLR1 protein levels validated by tissue microarray. We investigated correlations between IFNLR1 and clinical features, prognosis, CD4

resultsIn ccRCC, IFN-λ expression is elevated while IFNLR1 is significantly reduced compared to normal tissues, as confirmed by tissue microarrays. Lower IFNLR1 levels correlate with advanced tumor stage, poor grade, and worse prognosis, and show positive association with CD4

conclusionIFNLR1 may serve as a potential prognostic biomarker for ccRCC, with its expression levels reflecting the tumor immune microenvironment. Its predictive value for clinical immunotherapy efficacy remains to be established in prospective clinical cohorts.

Indexed as

Carcinoma, Renal CellDisease ProgressionKidney NeoplasmsLymphocytes, Tumor-InfiltratingReceptors, InterferonAnimalsB7-H1 AntigenCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansMicePrognosisTumor MicroenvironmentB7-H1 AntigenIFNLR1 protein, humanReceptors, InterferonBiomarkerIFNLR1Programmed cell death-ligand 1 (PD-L1)Renal cell carcinomaT cell infiltrationType III interferon (IFN-λ)

Identifiers

PMID42864662
PMCPMC13660129

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