Evidence map›Paper›PMID 27748763›Full record

ArticleOncogene2017

OmoMYC blunts promoter invasion by oncogenic MYC to inhibit gene expression characteristic of MYC-dependent tumors.

L A Jung, A Gebhardt, W Koelmel, C P Ade, S Walz, J Kuper, B von Eyss, S Letschert, C Redel, L d'Artista and 7 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.0field-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

58 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Beyond the Limit: MYC Mediates Tumor Immune Escape.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Mechanisms Involved in Therapeutic Effects ofBioMed research international · 2024
    Article
  16. Article
  17. Review
  18. Demystifying the Druggability of the MYC Family of Oncogenes.Journal of the American Chemical Society · 2023
    Review
  19. 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

17 authors at 5 institutions in 3 countries.

L A JungTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.
A GebhardtTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.
W KoelmelRudolf Virchow Center for Experimental Biomedicine, University of Würzburg, Würzburg, Germany.
C P AdeTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.
S WalzComprehensive Cancer Center, Core Unit Bioinformatics, Biocenter, Würzburg, Germany.
J KuperRudolf Virchow Center for Experimental Biomedicine, University of Würzburg, Würzburg, Germany.
B von EyssTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.
S LetschertDepartment of Biotechnology and Biophysics, Biocenter, University of Würzburg, Würzburg, Germany.
C RedelTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.
L d'ArtistaDivision of Translational Gastrointestinal Oncology, Department of Internal Medicine I, University of Tübingen, Tübingen, Germany.
A BiankinWolfson Wohl Cancer Research Centre, Institute of Cancer Sciences, University of Glasgow, Garscube Estate, Switchback Road, Bearsden, Glasgow, UK.
L ZenderDivision of Translational Gastrointestinal Oncology, Department of Internal Medicine I, University of Tübingen, Tübingen, Germany.
M SauerDepartment of Biotechnology and Biophysics, Biocenter, University of Würzburg, Würzburg, Germany.
E WolfTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.
G EvanDepartment of Biochemistry, University of Cambridge, Cambridge, UK.
C KiskerRudolf Virchow Center for Experimental Biomedicine, University of Würzburg, Würzburg, Germany.
M EilersTheodor Boveri Institute, Biocenter, University of Würzburg, Würzburg, Germany.ORCID 0000-0002-0376-6533
University of Würzburg · DEUniversity of Tübingen · DEComprehensive Cancer Center Mainfranken · DEGlasgow Royal Infirmary · GBUniversity of Cambridge · GB

Funding

Cancer Research UK 12077Cancer Research UK 17263Cancer Research UK 19013Cancer Research UK 22533Cancer Research UK 22585
6 · The paper itself

Abstract

MYC genes have both essential roles during normal development and exert oncogenic functions during tumorigenesis. Expression of a dominant-negative allele of MYC, termed OmoMYC, can induce rapid tumor regression in mouse models with little toxicity for normal tissues. How OmoMYC discriminates between physiological and oncogenic functions of MYC is unclear. We have solved the crystal structure of OmoMYC and show that it forms a stable homodimer and as such recognizes DNA in the same manner as the MYC/MAX heterodimer. OmoMYC attenuates both MYC-dependent activation and repression by competing with MYC/MAX for binding to chromatin, effectively lowering MYC/MAX occupancy at its cognate binding sites. OmoMYC causes the largest decreases in promoter occupancy and changes in expression on genes that are invaded by oncogenic MYC levels. A signature of OmoMYC-regulated genes defines subgroups with high MYC levels in multiple tumor entities and identifies novel targets for the eradication of MYC-driven tumors.

Indexed as

Promoter Regions, GeneticBinding SitesCells, CulturedDNAGene Expression Regulation, NeoplasticGenes, DominantHumansModels, MolecularNeoplasmsPeptide FragmentsProtein MultimerizationProto-Oncogene Proteins c-mycSequence HomologyTranscriptomeTumor Suppressor ProteinsDNAomomyc proteinPeptide FragmentsProto-Oncogene Proteins c-mycTumor Suppressor Proteins

Identifiers

PMID27748763
OpenAlexW2534930232

What OpenQuestion holds

Textmetadata
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.