Evidence map›Paper›PMID 41425556›Full record

ArticleFrontiers in immunology2025

Histone-related gene WDR77 promotes tumor progression through cell cycle regulation in skin cutaneous melanoma.

Haoxue Zhang, Ke Tang, Yuyao Liu, Shengxiu Liu

Abstract read
In one paragraph

Article in Frontiers in immunology, 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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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

4 authors.

Haoxue ZhangDepartment of Dermatovenerology, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Ke TangDepartment of Dermatovenerology, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yuyao LiuDepartment of Dermatovenerology, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Shengxiu LiuDepartment of Dermatovenerology, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Skin cutaneous melanoma (SKCM) is extremely malignant, leading to poor prognosis. Epigenetic dysregulation, particularly histone modifications, contributes to disease progression. However, effective histone-based prognostic biomarkers are still lacking in clinical practice. Methods: Transcriptomic data from TCGA-SKCM and five GEO datasets were analyzed. Ten machine learning algorithms were integrated to build 101 prognostic models. The optimal model, based on seven histone-related genes, showed the highest C-index and was validated in both training and validation cohorts. WDR77 was identified as the hub gene by random forest analysis. The expression of WDR77 was profiled in SKCM. Survival analysis, pathway enrichment analyses, single-cell and spatial transcriptomics were performed to investigate the role of WDR77 in SKCM. The therapeutic relevance of WDR77 was also investigated. In vitro experiments were conducted to validate the function of WDR77. Results: WDR77, a histone methylation factor working with PRMT5, was identified as a key candidate. WDR77 was significantly upregulated in SKCM and correlated with poor clinical outcomes. Pathway analysis showed that WDR77 was primarily associated with cell-cycle dysregulation. CDC20, a cell cycle factor, emerged as a key co-expressed gene. Patients with concurrent high expression of WDR77 and CDC20 had the worst survival outcomes. WDR77 was predominantly expressed in malignant cells across pan-cancer datasets and positively correlated with CDC20. Spatial transcriptomics confirmed their co-localization and co-upregulation in tumor regions. Functional experiments demonstrated that WDR77 promotes proliferation, migration, and cell cycle progression. Overexpression of WDR77 also increased CDC20 protein levels. Conclusion: WDR77 serves as both a prognostic biomarker and functional regulator in melanoma, highlighting its potential as a therapeutic target.

Indexed as

Cell CycleHistonesMelanomaSkin NeoplasmsBiomarkers, TumorCdc20 ProteinsCell Line, TumorCell ProliferationCutaneous Malignant MelanomaDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisBiomarkers, TumorCdc20 ProteinsHistonesCDC20cell cyclehistonemelanomaprognosis biomarkertherapeutic targetWDR77

Identifiers

PMID41425556
PMCPMC12711826

What Socratic holds

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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.