Evidence map›Paper›PMID 37308732›Full record

ArticleNature chemical biology2024

Direct stimulation of de novo nucleotide synthesis by O-GlcNAcylation.

Lulu Chen, Qi Zhou, Pingfeng Zhang, Wei Tan, Yingge Li, Ziwen Xu, Junfeng Ma, Gary M Kupfer, Yanxin Pei, Qibin Song and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Nature chemical biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

31 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Lung cancer metabolism: a dynamic and adaptive network.Cellular and molecular life sciences : CMLS · 2026
    Review
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  19. Glycosylation in kidney diseases.Precision clinical medicine · 2025
    Review
  20. 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

11 authors at 4 institutions in 2 countries.

Lulu ChenCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Qi ZhouCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Pingfeng ZhangCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.ORCID 0000-0001-5985-4914
Wei TanDepartment of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Yingge LiCancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Ziwen XuDepartment of Oncology, Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA.
Junfeng MaDepartment of Oncology, Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA.ORCID 0000-0002-5183-5425
Gary M KupferDepartment of Oncology, Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA.
Yanxin PeiCenter for Cancer and Immunology, Brain Tumor Institute, Children's National Health System, Washington, DC, USA.
Qibin SongCancer Center, Renmin Hospital of Wuhan University, Wuhan, China. qibinsong@whu.edu.cn.ORCID 0000-0002-4350-0916
Huadong PeiDepartment of Oncology, Georgetown Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA. huadong.pei@georgetown.edu.
Georgetown University · USWuhan University · CNChildren's National · USThe University of Texas MD Anderson Cancer Center · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
Mechanistic Dissection of the Fanconi Anemia Pathway of DNA Damage Response and RR01CA168635 · NCI · YALE UNIVERSITY · PI Gary M Kupfer, Patrick Sung · 2013 to 2026
$5.8M
Regulation of the Hedgehog pathway and Medulloblastoma response to radiochemotherapyR01NS121243 · NINDS · GEORGE WASHINGTON UNIVERSITY · PI PEI, HUADONG · 2021 to 2025
$1.9M
NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA168635NIH HHS RO1-CA68135NINDS NIH HHS R01 NS121243
6 · The paper itself

Abstract

O-linked β-N-acetyl glucosamine (O-GlcNAc) is at the crossroads of cellular metabolism, including glucose and glutamine; its dysregulation leads to molecular and pathological alterations that cause diseases. Here we report that O-GlcNAc directly regulates de novo nucleotide synthesis and nicotinamide adenine dinucleotide (NAD) production upon abnormal metabolic states. Phosphoribosyl pyrophosphate synthetase 1 (PRPS1), the key enzyme of the de novo nucleotide synthesis pathway, is O-GlcNAcylated by O-GlcNAc transferase (OGT), which triggers PRPS1 hexamer formation and relieves nucleotide product-mediated feedback inhibition, thereby boosting PRPS1 activity. PRPS1 O-GlcNAcylation blocked AMPK binding and inhibited AMPK-mediated PRPS1 phosphorylation. OGT still regulates PRPS1 activity in AMPK-deficient cells. Elevated PRPS1 O-GlcNAcylation promotes tumorigenesis and confers resistance to chemoradiotherapy in lung cancer. Furthermore, Arts-syndrome-associated PRPS1 R196W mutant exhibits decreased PRPS1 O-GlcNAcylation and activity. Together, our findings establish a direct connection among O-GlcNAc signals, de novo nucleotide synthesis and human diseases, including cancer and Arts syndrome.

Indexed as

AMP-Activated Protein KinasesProtein Processing, Post-TranslationalGlucoseHumansN-AcetylglucosaminyltransferasesNucleotidesPhosphorylationAMP-Activated Protein KinasesGlucoseN-AcetylglucosaminyltransferasesNucleotides

Identifiers

PMID37308732
PMCPMC10746546
OpenAlexW4380356647

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.