Evidence map›Paper›PMID 39791167›Full record

ArticleEndocrine, metabolic & immune disorders drug targets2025

Identification of Biomarkers Related to Liquid-Liquid Phase Separation for Ulcerative Colitis Based on Single-Cell and Bulk RNA Transcriptome Sequencing Data.

Jicheng Lu, Xu Lu, Bin Chen

Abstract read
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Article in Endocrine, metabolic & immune disorders drug targets, 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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1 · What the graph read from it

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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

3 authors.

Jicheng LuDepartment of Oncology, Suzhou Ninth People's Hospital, Suzhou, 215200, China.
Xu LuDepartment of Radiotherapy, Suzhou Ninth People's Hospital, Suzhou, 215200, China.ORCID 0000-0001-8314-1842
Bin ChenDepartment of Radiotherapy, Suzhou Ninth People's Hospital, Suzhou, 215200, China.

Funding

Wujiang district of Suzhou city "Science and education to promote health" project fund wwk202004
6 · The paper itself

Abstract

backgroundLiquid-Liquid Phase Separation (LLPS) is a process involved in the formation of established organelles and various condensates that lack membranes; however, the relationship between LLPS and Ulcerative Colitis (UC) remains unclear.

aimsThis study aimed to comprehensively clarify the correlation between ulcerative colitis (UC) and liquid-liquid phase separation (LLPS).

objectivesIn this study, bioinformatics analyses and public databases were applied to screen and validate key genes associated with LLPS in UC. Furthermore, the roles of these key genes in UC were comprehensively analyzed.

methodsBased on the single-cell transcriptomic data of UC obtained from the Gene Expression Omnibus (GEO) database, differences between patients with UC and their controls were compared using the limma package. The single-cell data were then filtered and normalized by the 'Seurat' package and subjected to dimension reduction by the Uniform Manifold Approximation and Projection (UMAP) algorithm. The LLPS-related genes (LLPSRGs) were searched on the Dr- LLPS website to obtain cross-correlated genes, which were scored using the ssGSEA algorithm. Next, functional enrichment, interaction network, immune landscape, and diagnostic and drug prediction of the LLPSRGs were comprehensively explored. Finally, the results were validated using external datasets and quantitative real-time PCR (qRT-PCR).

resultsA total of eight cell types in UC were classified, namely, fibroblasts, macrophages, endothelial cells, neutrophils, NK cells, B cells, epithelial cells, and T cells. The intersection between differently expressed genes (DEGs) among the eight cell types identified 44 key genes, which were predominantly enriched in immune- and infection-related pathways. According to receiver operating characteristic (ROC) curves,

conclusionThe LLPSRGs play crucial roles in UC and can be used as prognostic and diagnostic markers for UC. The current findings contribute to the management of UC.

Indexed as

Colitis, UlcerativeSequence Analysis, RNASingle-Cell AnalysisTranscriptomeBiomarkersComputational BiologyGene Expression ProfilingHumansPhase SeparationBiomarkersbiomarkers.gene set enrichment analysis (GSEA)inflammatory bowel diseaseLLPSsingle-cell sequencing analysisulcerative colitis

Identifiers

PMID39791167
PMCPMC12709534

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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 Socratic graph.