Evidence map›Paper›PMID 42316201›Full record

ArticleJournal of translational medicine2026

Crosstalk In: crosstalk-aware inference of tumor microenvironment cell infiltration.

Qianbei Yi, Jiaqi Yuan, Zheng Ye, Peng Xu, Wenbin Liu

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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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Qianbei YiInstitute of Computational Science and Technology, Guangzhou University, Guangzhou, 511370, China.
Jiaqi YuanInstitute of Computational Science and Technology, Guangzhou University, Guangzhou, 511370, China.
Zheng YeInstitute of Computational Science and Technology, Guangzhou University, Guangzhou, 511370, China.
Peng XuInstitute of Computational Science and Technology, Guangzhou University, Guangzhou, 511370, China.
Wenbin LiuInstitute of Computational Science and Technology, Guangzhou University, Guangzhou, 511370, China. wbliu6910@gzhu.edu.cn.ORCID 0000-0001-9091-3177

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe tumor microenvironment (TME) is a complex ecosystem whose cellular composition and interactions shape tumor progression, therapeutic response, and patient prognosis. However, most bulk deconvolution methods infer cell-type composition while treating cell types independently.

methodsIn this paper, we develop CrosstalkIn, a crosstalk-aware bulk deconvolution framework that constructs patient-specific cell-cell networks by integrating Gene Ontology (GO)-based functional similarity and protein-protein interaction (PPI)-based molecular relationships. A modified random walk with restart algorithm is then applied to calculate cell Infiltration Scores (InScores).

resultsBenchmark results on two flow-cytometry-validated cohorts demonstrate that CrosstalkIn achieves superior deconvolution performance, with the largest or second-largest Spearman correlations for most evaluated cell types. In lower-grade glioma, CrosstalkIn-derived InScores identify survival-associated cell types, generate accurate prognostic risk scores, and stratify patients into distinct survival groups. Across multiple adenocarcinoma cohorts, the risk score shows consistent prognostic value, particularly in advanced-stage patients. In melanoma, CrosstalkIn improves immunotherapy response prediction and identifies biologically interpretable cell-type biomarkers.

conclusionCrosstalkIn provides a robust framework for crosstalk-aware inference of TME cell infiltration from bulk transcriptomic data and supports cancer prognosis and immunotherapy response prediction.

Indexed as

Tumor MicroenvironmentAlgorithmsGene OntologyHumansImmunotherapyNeoplasmsPrognosisProtein Interaction Maps

Identifiers

PMID42316201
PMCPMC13528140

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