Evidence map›Paper›PMID 29150442›Full record

ArticleThe Journal of biological chemistry2017

Functional analyses of a human vascular tumor FOS variant identify a novel degradation mechanism and a link to tumorigenesis.

David G P van IJzendoorn, Zary Forghany, Frauke Liebelt, Alfred C Vertegaal, Aart G Jochemsen, Judith V M G Bovée, Karoly Szuhai, David A Baker

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
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  8. Review
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  11. Recurrent FOS rearrangement in proliferative fasciitis/proliferative myositis.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Loss of NF2 defines a genetic subgroup of non-FOS-rearranged osteoblastoma.The journal of pathology. Clinical research · 2020
    Article
  16. Article
  17. Utility of FOS as diagnostic marker for osteoid osteoma and osteoblastoma.Virchows Archiv : an international journal of pathology · 2020
    Article
  18. Experimental and therapeutic medicine · 2020
    Article
  19. What's new in bone forming tumours of the skeleton?Virchows Archiv : an international journal of pathology · 2020
    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

8 authors at 2 institutions in 1 country.

David G P van IJzendoornFrom the Departments of Pathology and.
Zary ForghanyMolecular Cell Biology, Leiden University Medical Center (LUMC), 2300 RC Leiden, The Netherlands.
Frauke LiebeltMolecular Cell Biology, Leiden University Medical Center (LUMC), 2300 RC Leiden, The Netherlands.
Alfred C VertegaalMolecular Cell Biology, Leiden University Medical Center (LUMC), 2300 RC Leiden, The Netherlands.
Aart G JochemsenMolecular Cell Biology, Leiden University Medical Center (LUMC), 2300 RC Leiden, The Netherlands.
Judith V M G BovéeFrom the Departments of Pathology and.
Karoly SzuhaiMolecular Cell Biology, Leiden University Medical Center (LUMC), 2300 RC Leiden, The Netherlands K.Szuhai@lumc.nl.
David A BakerMolecular Cell Biology, Leiden University Medical Center (LUMC), 2300 RC Leiden, The Netherlands d.baker@lumc.nl.
Leiden University Medical Center · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelioid hemangioma is a locally aggressive vascular neoplasm, found in bones and soft tissue, whose cause is currently unknown, but may involve oncogene activation. FOS is one of the earliest viral oncogenes to be characterized, and normal cellular FOS forms part of the activator protein 1 (AP-1) transcription factor complex, which plays a pivotal role in cell growth, differentiation, and survival as well as the DNA damage response. Despite this, a causal link between aberrant FOS function and naturally occurring tumors has not yet been established. Here, we describe a thorough molecular and biochemical analysis of a mutant FOS protein we identified in these vascular tumors. The mutant protein lacks a highly conserved helix consisting of the C-terminal four amino acids of FOS, which we show is indispensable for fast, ubiquitin-independent FOS degradation via the 20S proteasome. Our work reveals that FOS stimulates endothelial sprouting and that perturbation of normal FOS degradation could account for the abnormal vessel growth typical of epithelioid hemangioma. To the best of our knowledge, this is the first functional characterization of mutant FOS proteins found in tumors.

Indexed as

Angiogenesis Inducing AgentsCarcinogenesisCell DifferentiationCell Transformation, NeoplasticGene Expression Regulation, NeoplasticGenes, fosHemangiomaHumansProteasome Endopeptidase ComplexProteolysisProto-Oncogene Proteins c-fosRegulatory Elements, TranscriptionalVascular NeoplasmsAngiogenesis Inducing AgentsProteasome Endopeptidase ComplexProto-Oncogene Proteins c-fosangiogenesiscancer biologyc-Fosprotein degradationtranscription regulationvascular biology

Identifiers

PMID29150442
PMCPMC5766951
OpenAlexW2769690313

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.