Evidence map›Paper›PMID 41087652›Full record

ReviewExperimental & molecular medicine2025

The emerging landscape of brain glycosylation: from molecular complexity to therapeutic potential.

Youngsuk Seo, Ji Eun Park, Jae Young Yu, Boyoung Lee, Jong Hyuk Yoon, Hyun Joo An

Abstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Review
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  11. Multi-omics dissection of RAD21-PON1 axis reveals metabolic-immune crosstalk and prognostic significance in hepatocellular carcinoma.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Youngsuk SeoCenter for Memory and Glioscience, Life Science Institute, Institute for Basic Science, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0002-8934-3290
Ji Eun ParkAsia-Pacific Glycomics Reference Site, Daejeon, Republic of Korea.
Jae Young YuAsia-Pacific Glycomics Reference Site, Daejeon, Republic of Korea.
Boyoung LeeCenter for Memory and Glioscience, Life Science Institute, Institute for Basic Science, Daejeon, Republic of Korea.ORCID http://orcid.org/0000-0001-9445-510X
Jong Hyuk YoonNeurodegenerative Diseases Research Group, Korea Brain Research Institute, Daegu, Republic of Korea.ORCID http://orcid.org/0000-0002-4090-3832
Hyun Joo AnAsia-Pacific Glycomics Reference Site, Daejeon, Republic of Korea. hjan@cnu.ac.kr.

Funding

Ministry of Science, ICT and Future Planning (MSIP) No. 25-BR-06-01Ministry of Trade, Industry and Energy (Ministry of Trade, Industry and Energy, Korea) No.22-CM-EC-18
6 · The paper itself

Abstract

Glycosylation functions as a pivotal posttranslational modification in proteins and as a distinct biosynthetic process in lipids. In the brain, it plays essential roles in development, function and homeostasis by modulating protein folding, receptor trafficking and intercellular communication. Although glycans constitute less than 1% of the brain's mass, their impact is disproportionately profound. Recent technological advances have uncovered the essential contributions of both protein- and lipid-bound glycans, including N-glycans, O-glycans and gangliosides, to brain physiology and disease. Here we explore the emerging landscape of brain glycosylation, highlighting its distinct roles in neurodevelopment, synaptic organization and immune regulation. Aberrant glycosylation has been implicated in neurodegenerative diseases (for example, Alzheimer's and Parkinson's), psychiatric disorders (for example, depression and schizophrenia) and neurodevelopmental conditions (for example, autism spectrum disorders, attention deficit hyperactivity disorder and dystroglycanopathies). We summarize recent breakthroughs in glycomics technologies, including glycan enrichment, liquid chromatography-tandem mass spectrometry, MALDI-based imaging mass spectrometry and high-throughput omics, which enable molecular and spatial mapping of brain glycosylation. Artificial-intelligence-driven bioinformatics and multi-omics integration are rapidly opening new avenues for deciphering glycan-mediated regulation in brain health and disease. Together, these developments position brain glycosylation as a transformative frontier in neuroscience, with the potential to yield novel diagnostic biomarkers and therapeutic strategies for complex brain disorders.

Indexed as

BrainAnimalsGlycomicsGlycosylationHumansNeurodegenerative DiseasesPolysaccharidesProtein Processing, Post-TranslationalPolysaccharides

Identifiers

PMID41087652
PMCPMC12586631

What OpenQuestion holds

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LicenceCC BY
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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.