Evidence map›Paper›PMID 31149037›Full record

ArticleTheranostics2019

High OGT activity is essential for MYC-driven proliferation of prostate cancer cells.

Harri M Itkonen, Alfonso Urbanucci, Sara Es Martin, Aziz Khan, Anthony Mathelier, Bernd Thiede, Suzanne Walker, Ian G Mills

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

53 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
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  14. CanPharmaceuticals (Basel, Switzerland) · 2024
    Review
  15. Article
  16. H3K4me3 remodeling induced acquired resistance through O-GlcNAc transferase.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2023
    Article
  17. Article
  18. Article
  19. The world journal of men's health · 2023
    Article
  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

8 authors at 5 institutions in 3 countries.

Harri M ItkonenCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Alfonso UrbanucciCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Sara Es MartinDepartment of Microbiology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Aziz KhanCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Anthony MathelierCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Bernd ThiedeDepartment of Biosciences, University of Oslo, Oslo, Norway.
Suzanne WalkerDepartment of Microbiology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Ian G MillsCentre for Molecular Medicine Norway (NCMM), Nordic EMBL Partnership, University of Oslo, Oslo, Norway.
Boston VA Research Institute · USOslo University Hospital · NOUniversity of Oslo · NOHarvard University · USUniversity of Oxford · GB

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Structure, Function and Inhibition of Human O-GlcNAc TransferaseR01GM094263 · NIGMS · HARVARD MEDICAL SCHOOL · PI WALKER, SUZANNE · 2012 to 2024
$5.8M
Functional Proteomics by Reverse Phase Protein Array in CancerR50CA221675 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LU, YILING · 2017 to 2021
$726k
NCI NIH HHS P30 CA016672NCI NIH HHS R50 CA221675NIGMS NIH HHS R01 GM094263
6 · The paper itself

Abstract

O-GlcNAc transferase (OGT) is overexpressed in aggressive prostate cancer. OGT modifies intra-cellular proteins via single sugar conjugation (O-GlcNAcylation) to alter their activity. We recently discovered the first fast-acting OGT inhibitor OSMI-2. Here, we probe the stability and function of the chromatin O-GlcNAc and identify transcription factors that coordinate with OGT to promote proliferation of prostate cancer cells.

Indexed as

Cell ProliferationAnimalsCell Line, TumorCells, CulturedChromatinChromatin Assembly and DisassemblyCyclin B1Enhancer Elements, GeneticHost Cell Factor C1HumansMaleMiceN-AcetylglucosaminyltransferasesProstatic NeoplasmsProto-Oncogene Proteins c-mycTranscriptional ActivationChromatinCyclin B1HCFC1 protein, humanHost Cell Factor C1N-AcetylglucosaminyltransferasesProto-Oncogene Proteins c-mycUDP-N-acetylglucosamine-peptide beta-N-acetylglucosaminyltransferaseglycosylationMYCO-GlcNAc transferaseprostate cancersuper-enhancer

Identifiers

PMID31149037
PMCPMC6531294
OpenAlexW2938707984

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.