Evidence map›Paper›PMID 32555333›Full record

ArticleOncogene2020

Mdm2-mediated neddylation of pVHL blocks the induction of antiangiogenic factors.

Eric R Wolf, Alexander R Mabry, Blossom Damania, Lindsey D Mayo

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

23 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Von Hippel-Lindau/Hypoxia Inducible Factor Axis in Glioblastoma.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Induction of the Mdm2 gene and protein by kinase signaling pathways is repressed by the pVHL tumor suppressor.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  11. Protein neddylation and its role in health and diseases.Signal transduction and targeted therapy · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. MDM2- an indispensable player in tumorigenesis.Molecular biology reports · 2023
    Review
  17. Review
  18. Article
  19. 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

4 authors at 2 institutions in 1 country.

Eric R WolfDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Alexander R MabryDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.ORCID http://orcid.org/0000-0003-1635-8800
Blossom DamaniaDepartment of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC, 27599, USA.
Lindsey D MayoDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, IN, 46202, USA. ldmayo@iu.edu.ORCID http://orcid.org/0000-0002-5997-5166
Indiana University School of MedicineUniversity of North Carolina at Chapel Hill · US

Funding

Regulation of Mdm2 activity by kinase signaling pathwaysR01CA172256 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI MAYO, LINDSEY D · 2013 to 2017
$1.8M
NCI NIH HHS R01 CA172256
6 · The paper itself

Abstract

Mutations in the tumor suppressor TP53 are rare in renal cell carcinomas. p53 is a key factor for inducing antiangiogenic genes and RCC are highly vascularized, which suggests that p53 is inactive in these tumors. One regulator of p53 is the Mdm2 oncogene, which is correlated with high-grade, metastatic tumors. However, the sole activity of Mdm2 is not just to regulate p53, but it can also function independent of p53 to regulate the early stages of metastasis. Here, we report that the oncoprotein Mdm2 can bind directly to the tumor suppressor VHL, and conjugate nedd8 to VHL within a region that is important for the p53-VHL interaction. Nedd8 conjugated VHL is unable to bind to p53 thereby preventing the induction of antiangiogenic factors. These results highlight a previously unknown oncogenic function of Mdm2 during the progression of cancer to promote angiogenesis through the regulation of VHL. Thus, the Mdm2-VHL interaction represents a pathway that impacts tumor angiogenesis.

Indexed as

Angiogenesis InhibitorsAnimalsCell Line, TumorHumansMiceProto-Oncogene Proteins c-mdm2TransfectionVon Hippel-Lindau Tumor Suppressor ProteinAngiogenesis InhibitorsMDM2 protein, humanProto-Oncogene Proteins c-mdm2VHL protein, humanVon Hippel-Lindau Tumor Suppressor Protein

Identifiers

PMID32555333
PMCPMC7368819
OpenAlexW3036121585

What OpenQuestion holds

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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.