Evidence map›Paper›PMID 20883453›Full record

ArticlePigment cell & melanoma research2011

Clinical relevance of SKP2 alterations in metastatic melanoma.

Amy E Rose, Guimin Wang, Douglas Hanniford, Stefano Monni, Ting Tu, Richard L Shapiro, Russell S Berman, Anna C Pavlick, Michele Pagano, Farbod Darvishian and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Pigment cell & melanoma research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

30 citing papers in PubMed, 54 citations in OpenAlex.

  1. E3 ubiquitin ligase SKP2 limits autophagosome formation duringFrontiers in cellular and infection microbiology · 2026
    Article
  2. A pan-cancer analysis revealedPrecision clinical medicine · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Frontiers in oncology · 2019
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Expression of Skp2 and p27Oncology letters · 2015
    Article
  20. Dysregulation of ubiquitin ligases in cancer.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2015
    Review
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

13 authors at 4 institutions in 1 country.

Amy E RoseRonald O. Perelman Department of Dermatology, New York University School of Medicine, New York, NY, USA.
Guimin Wang
Douglas Hanniford
Stefano Monni
Ting Tu
Richard L Shapiro
Russell S Berman
Anna C Pavlick
Michele Pagano
Farbod Darvishian
Madhu Mazumdar
Eva Hernando
Iman Osman
New York University · USEastern Cooperative Oncology Group · USCornell University · USHoward Hughes Medical Institute · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Drew R Jones · 1985 to 2026
$83.1M
REGULATION OF THE GI PHASE BY THE UBIQUITIN PATHWAYR01GM057587 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PAGANO, MICHELE · 1998 to 2018
$7.8M
F-box proteins: deregulated cell cycle control and proteolysis in cancerR37CA076584 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PAGANO, MICHELE · 2006 to 2016
$4.7M
The Study of E3 Ligases and LongevityR21AG032560 · NIA · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI DILLIN, ANDREW G · 2008 to 2009
$519k
Role of the SCF/Fbxo15 ubiquitin ligase in stem cells and cancer biologyR21CA161108 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PAGANO, MICHELE · 2011 to 2012
$404k
Howard Hughes Medical InstituteNCI NIH HHS 5 P30 CA 016087-27NCI NIH HHS P30 CA016087NCI NIH HHS R21 CA161108NCI NIH HHS R37 CA076584NCI NIH HHS R37-CA076584NIA NIH HHS R21 AG032560NIA NIH HHS R21-AG032560NIGMS NIH HHS R01 GM057587NIGMS NIH HHS R01-GM057587
6 · The paper itself

Abstract

In this study, we investigated the mechanism(s) of altered expression of protooncogene SKP2 in metastatic melanoma and its clinical relevance in patients with metastatic melanoma. The genomic status of SKP2 was assessed in cell lines by sequencing, single nucleotide polymorphism array, and genomic PCR. Copy number status was then evaluated for concordance with SKP2 mRNA and protein expression. SKP2 protein was further evaluated by immunohistochemistry in 93 human metastatic tissues. No mutations were identified in SKP2. Increased copy number at the SKP2 locus was observed in 6/14 (43%) metastatic cell lines and in 9/22 (41%) human metastatic tissues which was associated with overexpression of SKP2 protein. Overexpression of SKP2 protein in human tissues was associated with worse survival in a multivariate model controlling for the site of metastasis. Copy number gain is a major contributing mechanism of SKP2 overexpression in metastatic melanoma. Results may have implications for the development of therapeutics that target SKP2.

Indexed as

Cdh1 ProteinsCell CycleCell Cycle ProteinsCell Line, TumorCyclin-Dependent Kinase Inhibitor p27FemaleGene DosageGene Expression Regulation, NeoplasticGenetic LociHumansMaleMelanomaMiddle AgedNeoplasm MetastasisNucleotidesOpen Reading FramesCdh1 ProteinsCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p27FZR1 protein, humanNucleotidesS-Phase Kinase-Associated Proteins

Identifiers

PMID20883453
PMCPMC3341662
OpenAlexW2137924973

What OpenQuestion holds

Textmetadata
LicenceTDM
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.