Evidence map›Paper›PMID 16380502›Full record

ReviewMolecular cancer research : MCR2005

The emerging role of the COP9 signalosome in cancer.

Katharine S Richardson, Wayne Zundel

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular cancer research : MCR, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

64 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2024
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  12. Structural dynamics of the human COP9 signalosome revealed by cross-linking mass spectrometry and integrative modeling.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  13. Observational
  14. Review
  15. Article
  16. Article
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4 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Katharine S RichardsonDepartment of Pharmacology, James Graham Brown Cancer Center, University of Louisville School of Medicine, Louisville, KY 40202, USA.
Wayne Zundel
University of Louisville · US

Funding

CSN5 Mediates HIF-alpha Stability and Tumor GrowthR01CA102301 · NCI · UNIVERSITY OF LOUISVILLE · PI ZUNDEL, WAYNE S · 2004 to 2007
$909k
NCI NIH HHS R01 CA102301NCI NIH HHS R01-CA102301
6 · The paper itself

Abstract

In the last several years, multiple lines of evidence have suggested that the COP9 signalosome (CSN) plays a significant role in the regulation of multiple cancers and could be an attractive target for therapeutic intervention. First, the CSN plays a key role in the regulation of Cullin-containing ubiquitin E3 ligases that are central mediators of a variety of cellular functions essential during cancer progression. Second, several studies suggest that the individual subunits of the CSN, particularly CSN5, might regulate oncogenic and tumor suppressive functions independently of, or coordinately with, the CSN holocomplex. Thus, deregulation of CSN subunit function can have a dramatic effect on diverse cellular functions, including the maintenance of DNA fidelity, cell cycle control, DNA repair, angiogenesis, and microenvironmental homeostasis that are critical for tumor development. Additionally, clinical studies have suggested that the expression or localization of some CSN subunits correlate to disease progression or clinical outcome in a variety of tumor types. Although the study of CSN function in relation to tumor progression is in its infancy, this review will address current studies in relation to cancer initiation, progression, and potential for therapeutic intervention.

Indexed as

AnimalsCell CycleCOP9 Signalosome ComplexCullin ProteinsDNA DamageDNA RepairHumansMultiprotein ComplexesNeoplasmsNeovascularization, PathologicPeptide HydrolasesSignal TransductionCOP9 Signalosome ComplexCullin ProteinsMultiprotein ComplexesPeptide Hydrolases

Identifiers

PMID16380502
PMCPMC2943958
OpenAlexW2162877061

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.