Evidence map›Paper›PMID 40626556›Full record

ArticleNucleic acids research2025

DiCE: differential centrality-ensemble analysis based on gene expression profiles and protein-protein interaction network.

Elnaz Pashaei, Sheng Liu, Kailing Li, Yong Zang, Lei Yang, Tim Lautenschlaeger, Jun Huang, Xin Lu, Jun Wan

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Elnaz PashaeiDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Sheng LiuDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Kailing LiDepartment of BioHealth Informatics, Luddy School of Informatics and Computing, Indiana University at Indianapolis, Indianapolis, IN 46202, United States.
Yong ZangDepartment of Biostatistics and Health Data Science, Indiana University School of Medicine, Indianapolis, IN 46202, United States.ORCID 0000-0003-0572-4756
Lei YangCenter for Computational Biology and Bioinformatics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.ORCID 0000-0002-1479-2374
Tim LautenschlaegerIndiana University Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Jun HuangPritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, United States.
Xin LuIndiana University Simon Comprehensive Cancer Center, Indiana University School of Medicine, Indianapolis, IN 46202, United States.
Jun WanDepartment of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, United States.ORCID 0000-0001-9286-6562

Funding

Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI David W Clapp · 1999 to 2026
$59.3M
Converting Cold to Hot Tumor Microenvironment in Prostate Cancer by Targeting Chromatin EffectorR01CA248033 · NCI · UNIVERSITY OF NOTRE DAME · PI LU, XIN · 2020 to 2024
$1.8M
Immunosuppression and Metabolic Rewiring in Tumor-infiltrating NeutrophilsR01CA280097 · NCI · UNIVERSITY OF NOTRE DAME · PI Xin Lu · 2023 to 2026
$1.4M
Department of Defense HT94252310010Department of Defense HT94252310613Department of Defense W81XWH2010312Indiana University School of MedicineIndiana University Simon Comprehensive Cancer CenterIndiana University Simon Comprehensive Cancer Center P30CA082709NCI NIH HHS P30 CA082709NCI NIH HHS R01 CA248033NCI NIH HHS R01 CA280097NIH HHSNIH HHS R01CA248033NIH HHS R01CA280097Ralph W. and Grace M. Showalter Research Trust FundWalther Cancer Foundation
6 · The paper itself

Abstract

Uncovering key genes that drive diseases and cancers is crucial for advancing understanding and developing targeted therapies. Traditional differential expression analysis often relies on arbitrary cutoffs, missing critical genes with subtle expression changes. Some methods incorporate protein-protein interactions (PPIs) but depend on prior disease knowledge. To address these challenges, we developed DiCE (Differential Centrality-Ensemble analysis), a novel approach that combines differential expression with network centrality analysis, independent of prior disease annotations. DiCE identifies candidate genes, refines them with an information gain filter, and reconstructs a condition-specific weighted PPI network. Using centrality measures, DiCE ranks genes based on expression shifts and network influence. Validated on prostate cancer datasets, DiCE identified genes overrepresented in key pathways and cancer fitness genes, significantly correlating with disease-free survival (DFS), despite DFS not being used in selection. DiCE offers a comprehensive, unbiased approach to identifying disease-associated genes, advancing biomarker discovery and therapeutic development.

Indexed as

Gene Expression ProfilingProstatic NeoplasmsProtein Interaction MappingProtein Interaction MapsSoftwareTranscriptomeAlgorithmsDisease-Free SurvivalGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMale

Identifiers

PMID40626556
PMCPMC12235518

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Registered trials

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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.