Evidence map›Paper›PMID 25605410›Full record

ReviewEndocrine-related cancer2015

Deubiquitinases and the new therapeutic opportunities offered to cancer.

Roland Pfoh, Ira Kay Lacdao, Vivian Saridakis

Abstract readReview
In one paragraph

Review in Endocrine-related cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
–field-weighted citation impact
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

88 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Role of the USP family in autophagy regulation and cancer progression.Apoptosis : an international journal on programmed cell death · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

28 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

3 authors.

Roland PfohDepartment of BiologyYork University, 4700 Keele Street, Toronto, Ontario, Canada, M3J1P3.
Ira Kay LacdaoDepartment of BiologyYork University, 4700 Keele Street, Toronto, Ontario, Canada, M3J1P3.
Vivian SaridakisDepartment of BiologyYork University, 4700 Keele Street, Toronto, Ontario, Canada, M3J1P3 vsaridak@yorku.ca.

Funding

Canadian Institutes of Health Research 106583
6 · The paper itself

Abstract

Deubiquitinases (DUBs) play important roles and therefore are potential drug targets in various diseases including cancer and neurodegeneration. In this review, we recapitulate structure-function studies of the most studied DUBs including USP7, USP22, CYLD, UCHL1, BAP1, A20, as well as ataxin 3 and connect them to regulatory mechanisms and their growing protein interaction networks. We then describe DUBs that have been associated with endocrine carcinogenesis with a focus on prostate, ovarian, and thyroid cancer, pheochromocytoma, and adrenocortical carcinoma. The goal is enhancing our understanding of the connection between dysregulated DUBs and cancer to permit the design of therapeutics and to establish biomarkers that could be used in diagnosis and prognosis.

Indexed as

AnimalsHumansMolecular Targeted TherapyNeoplasmsSignal TransductionUbiquitinUbiquitin-Protein LigasesUbiquitin-Specific ProteasesUbiquitin ThiolesteraseUbiquitinUbiquitin-Protein LigasesUbiquitin-Specific ProteasesUbiquitin ThiolesteraseA20ataxin 3BAP1CYLDdeubiquitinasesUCHL1USP22USP7

Identifiers

PMID25605410
PMCPMC4304536

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.