Evidence map›Paper›PMID 41835303›Full record

ArticleBioinformatics advances2026

A kernel density estimation-based approach for quantifying O-GlcNAcylation dysregulation in cancer from gene expression data.

Rastko Stojšin, Jinlian Wang, Hongfang Liu

Abstract read
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Article in Bioinformatics advances, 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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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.

Rastko StojšinCenter for Translational AI Excellence and Applications in Medicine, D. Bradley McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.ORCID https://orcid.org/0000-0001-5545-1181
Jinlian WangCenter for Translational AI Excellence and Applications in Medicine, D. Bradley McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.
Hongfang LiuCenter for Translational AI Excellence and Applications in Medicine, D. Bradley McWilliams School of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, TX 77030, United States.ORCID https://orcid.org/0000-0003-2570-3741

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: O-GlcNAcylation, a dynamic post-translational modification regulated by O-GlcNAc transferase (OGT) and O-GlcNAcase (OGA), influences critical biological processes and is dysregulated in cancers. Direct measurement of O-GlcNAcylation dysregulation is challenging due to its instability and low-throughput nature, limiting large-scale studies. However, the regulatory simplicity of this system and the availability of transcriptomic data enable inference of dysregulation from OGT and OGA expression. Results: We introduce a nonparametric kernel density estimation-based approach to quantify O-GlcNAcylation dysregulation using joint OGT and OGA expression. In simulated datasets with varied expression patterns and controlled dysregulation levels, our method consistently outperformed canonical metrics in quantifying dysregulation. In TCGA data from six cancer types, inferred regulation scores were significantly lower in cancer samples (0.25-0.30 vs. 0.49-0.51) and showed strong distributional differences (Kolmogorov-Smirnov Availability and implementation: The code and datasets used in this study are freely available at https://github.com/wonder-ai/O-GlcNAcylation_Project under an open-source license.

Identifiers

PMID41835303
PMCPMC12980335

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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.