Evidence map›Paper›PMID 26432751›Full record

ReviewSeminars in cancer biology2016

Deregulation of F-box proteins and its consequence on cancer development, progression and metastasis.

Jinho Heo, Rebeka Eki, Tarek Abbas

Abstract readReview
In one paragraph

Review in Seminars in cancer biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.9field-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

35 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. F-box in breast cancer: mechanism of action and therapeutic potential.American journal of translational research · 2025
    Review
  6. Article
  7. Molecular insights and clinical implications for the tumor suppressor role of SCFBiochimica et biophysica acta. Reviews on cancer · 2024
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. F-box only protein 9 and its role in cancer.Molecular biology reports · 2022
    Review
  13. Association of FBXW11 levels with tumor development and prognosis in chondrosarcoma.Cancer biomarkers : section A of Disease markers · 2022
    Article
  14. Article
  15. Review
  16. 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

3 authors at 1 institution in 1 country.

Jinho HeoDepartment of Radiation Oncology, University of Virginia, Charlottesville, VA, USA.
Rebeka EkiDepartment of Radiation Oncology, University of Virginia, Charlottesville, VA, USA; Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA, USA.
Tarek AbbasDepartment of Radiation Oncology, University of Virginia, Charlottesville, VA, USA; Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, VA, USA; Center for Cell Signaling, University of Virginia, Charlottesville, VA, USA. Electronic address: ta8e@virginia.edu.
University of Virginia · US

Funding

Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
The Role of CRL4-Cdt2 E3 Ubiquitin Ligase in Genomic Stability and CancerR00CA140774 · NCI · UNIVERSITY OF VIRGINIA · PI ABBAS, TAREK A. · 2012 to 2014
$725k
NCI NIH HHS CA009109NCI NIH HHS R00 CA140774NCI NIH HHS T32 CA009109
6 · The paper itself

Abstract

F-box proteins are substrate receptors of the SCF (SKP1-Cullin 1-F-box protein) E3 ubiquitin ligase that play important roles in a number of physiological processes and activities. Through their ability to assemble distinct E3 ubiquitin ligases and target key regulators of cellular activities for ubiquitylation and degradation, this versatile group of proteins is able to regulate the abundance of cellular proteins whose deregulated expression or activity contributes to disease. In this review, we describe the important roles of select F-box proteins in regulating cellular activities, the perturbation of which contributes to the initiation and progression of a number of human malignancies.

Indexed as

AnimalsApoptosisCell SurvivalCell Transformation, NeoplasticDisease ProgressionF-Box ProteinsGene Expression Regulation, NeoplasticGenomic InstabilityHumansNeoplasm MetastasisNeoplasmsOncogene ProteinsProteomeTumor Suppressor ProteinsUbiquitinsF-Box ProteinsOncogene ProteinsProteomeTumor Suppressor ProteinsUbiquitinsCancerE3 ubiquitin ligasesF-boxSCFUbiquitin

Identifiers

PMID26432751
PMCPMC4761475
OpenAlexW2180612428

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.