Evidence map›Paper›PMID 39256595›Full record

ArticleEMBO reports2024

O-GlcNAcylation mediates Wnt-stimulated bone formation by rewiring aerobic glycolysis.

Chengjia You, Fangyuan Shen, Puying Yang, Jingyao Cui, Qiaoyue Ren, Moyu Liu, Yujie Hu, Boer Li, Ling Ye, Yu Shi

Abstract read
In one paragraph

Article in EMBO reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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  12. O-GlcNAcylation in Gli1International journal of molecular sciences · 2025
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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

10 authors.

Chengjia YouState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.ORCID 0000-0002-3423-7167
Fangyuan ShenState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Puying YangState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Jingyao CuiState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Qiaoyue RenState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Moyu LiuState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Yujie HuDepartment of Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Boer LiState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Ling YeState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China. yeling@scu.edu.cn.ORCID 0000-0002-8417-7676
Yu ShiState Key Laboratory of Oral Diseases and National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China. yushi1105@scu.edu.cn.ORCID 0000-0001-5039-0877

Funding

MOST | National Natural Science Foundation of China (NSFC) 82001040MOST | National Natural Science Foundation of China (NSFC) 82071091MOST | NSFC | National Science Fund for Distinguished Young Scholars (National Science Foundation for Distinguished Young Scholars) 81825005SCU | West China School of Stomatology, Sichuan University (WCSS) QDJF2021-1SCU | West China School of Stomatology, Sichuan University (WCSS) RD-03-202304
6 · The paper itself

Abstract

Wnt signaling is an important target for anabolic therapies in osteoporosis. A sclerostin-neutralizing antibody (Scl-Ab), that blocks the Wnt signaling inhibitor (sclerostin), has been shown to promote bone mass in animal models and clinical studies. However, the cellular mechanisms by which Wnt signaling promotes osteogenesis remain to be further investigated. O-GlcNAcylation, a dynamic post-translational modification of proteins, controls multiple critical biological processes including transcription, translation, and cell fate determination. Here, we report that Wnt3a either induces O-GlcNAcylation rapidly via the Ca

Indexed as

GlycolysisOsteoblastsOsteogenesisWnt3A ProteinWnt Signaling PathwayAcylationAnimalsbeta CateninCyclic AMP-Dependent Protein KinasesGlycosylationHumansMiceProtein Processing, Post-Translationalbeta CateninCyclic AMP-Dependent Protein KinasesWnt3A ProteinWnt3a protein, mouseBone FormationFracture HealingGlucose MetabolismO-GlcNAcylationWnt

Identifiers

PMID39256595
PMCPMC11467389

What OpenQuestion holds

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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.