Evidence map›Paper›PMID 25003721›Full record

ArticleOncotarget2014

Usp7 protects genomic stability by regulating Bub3.

Serena Giovinazzi, Pietro Sirleto, Vasilisa Aksenova, Viacheslav M Morozov, Roberto Zori, William C Reinhold, Alexander M Ishov

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Deubiquitinases in cancer.Nature reviews. Cancer · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. USP7 Is a Master Regulator of Genome Stability.Frontiers in cell and developmental biology · 2020
    Review
  8. Genome-wide DNA copy number analysis and targeted transcriptional analysis of canine histiocytic malignancies identifies diagnostic signatures and highlights disruption of spindle assembly complex.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2019
    Article
  9. Review
  10. Article
  11. Article
  12. Decision for cell fate: deubiquitinating enzymes in cell cycle checkpoint.Cellular and molecular life sciences : CMLS · 2016
    Review
  13. Review
  14. Article
  15. 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

7 authors at 4 institutions in 3 countries.

Serena GiovinazziDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL; University of Florida Health Cancer Center, Gainesville, FL.
Pietro Sirleto
Vasilisa Aksenova
Viacheslav M Morozov
Roberto Zori
William C Reinhold
Alexander M IshovDepartment of Anatomy and Cell Biology, University of Florida College of Medicine, Gainesville, FL; University of Florida Health Cancer Center, Gainesville, FL.
University of Florida Health · USFlorida College · USInstitute of Cytology · RUNational Cancer Institute · US

Funding

Function of Daxx in mitosis that determines paclitaxel sensitivity in breast cancR01CA127378 · NCI · UNIVERSITY OF FLORIDA · PI ISHOV, ALEXANDER M · 2007 to 2011
$1.4M
Intramural NIH HHSNCI NIH HHS R01 CA127378NCI NIH HHS R01 CA127378-01A1
6 · The paper itself

Abstract

USP7 (Ubiquitin Specific processing Protease-7) is a deubiquitinase which, over the past decade emerged as a critical regulator of cellular processes. Deregulation of USP7 activity has been linked to cancer, making USP7 inhibition an appealing anti-cancer strategy. The identification of novel USP7 substrates and additional USP7-dependent cellular activities will broaden our knowledge towards potential clinical application of USP7 inhibitors. Results presented in this study uncover a novel and pivotal function of USP7 in the maintenance of genomic stability. Upon USP7 depletion we observed prolonged mitosis and mitotic abnormalities including micronuclei accumulation, lagging chromosomes and karyotype instability. Inhibition of USP7 with small molecule inhibitors stabilizes cyclin B and causes mitotic abnormalities. Our results suggest that these USP7-dependent effects are mediated by decreased levels of spindle assembly checkpoint (SAC) component Bub3, which we characterized as an interacting partner and substrate of USP7. In silico analysis across the NCI-60 panels of cell lines supports our results where lower levels of USP7 strongly correlate with genomic instability. In conclusion, we identified a novel role of USP7 as regulator of the SAC component Bub3 and genomic stability.

Indexed as

Cell Cycle ProteinsGene ExpressionGenomic InstabilityHCT116 CellsHEK293 CellsHumansNeoplasmsPoly-ADP-Ribose Binding ProteinsTransfectionUbiquitin-Specific Peptidase 7Ubiquitin ThiolesteraseBUB3 protein, humanCell Cycle ProteinsPoly-ADP-Ribose Binding ProteinsUbiquitin-Specific Peptidase 7Ubiquitin ThiolesteraseUSP7 protein, human

Identifiers

PMID25003721
PMCPMC4116516
OpenAlexW1504025592

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.