Evidence map›Paper›PMID 27121063›Full record

ArticleOncotarget2016

USP14 is a predictor of recurrence in endometrial cancer and a molecular target for endometrial cancer treatment.

Rachel Isaksson Vogel, Tanya Pulver, Wiebke Heilmann, Ashley Mooneyham, Sally Mullany, Xianda Zhao, Maryam Shahi, James Richter, Molly Klein, Liqiang Chen and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.7field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. AKT and DUBs: a bidirectional relationship.Cellular & molecular biology letters · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Deubiquitinases: Modulators of Different Types of Regulated Cell Death.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Role of Deubiquitinases in Human Cancers: Potential Targeted Therapy.International journal of molecular sciences · 2020
    Review
  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

16 authors at 3 institutions in 2 countries.

Rachel Isaksson VogelMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Tanya PulverMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Wiebke HeilmannMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Ashley MooneyhamMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Sally MullanyMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Xianda ZhaoDivision of Basic and Translational Research, Department of Surgery, University of Minnesota, Minneapolis, MN, USA.
Maryam ShahiDepartment of Pathology and Laboratory Medicine, University of Minnesota, Minneapolis, MN, USA.
James RichterDepartment of Pathology and Laboratory Medicine, University of Minnesota, Minneapolis, MN, USA.
Molly KleinDepartment of Pathology and Laboratory Medicine, University of Minnesota, Minneapolis, MN, USA.
Liqiang ChenCenter for Drug Design, Academic Health Center, University of Minnesota, Minneapolis, MN, USA.
Rui DingCenter for Drug Design, Academic Health Center, University of Minnesota, Minneapolis, MN, USA.
Gottfried KonecnyGynecologic Oncology, Hematology & Oncology Department, UCLA Medical Center, Santa Monica, CA, USA.
Stefan KommossDepartment of Women's Health, University Hospital Tuebingen University, Tuebingen, Germany.
Boris WinterhoffMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Rahel GhebreMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
Martina BazzaroMasonic Cancer Center and Department of Obstetrics, Gynecology and Women's Health, University of Minnesota, Minneapolis, MN, USA.
University of Minnesota · USUCLA Medical Center · USUniversity of Tübingen · DE

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Douglas Yee · 1998 to 2026
$100.4M
University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UL1TR000114 · NCATS · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R · 2012 to 2015
$35.0M
NCATS NIH HHS UL1 TR000114NCI NIH HHS P30 CA077598
6 · The paper itself

Abstract

Endometrial adenocarcinoma is the most common gynecologic malignancy in the United States. Most endometrial cancer cases are diagnosed at an early stage and have good prognosis. Unfortunately a subset of patients with early stage and low grade disease experience recurrence for reasons that remain unclear. Recurrence is often accompanied by chemoresistance and high mortality.Deubiquitinating enzymes (DUBs) are key components of the ubiquitin-dependent protein degradation pathway and act as master regulators in a number of metabolic processes including cell growth, differentiation, and apoptosis. DUBs have been shown to be upregulated in a number of human cancers and their aberrant activity has been linked to cancer progression, initiation and onset of chemoresistance. Thus, selective inhibition of DUBs has been proposed as a targeted therapy for cancer treatment.This study suggests the DUB USP14 as a promising biomarker for stratifying endometrial cancer patients at diagnosis based on their risk of recurrence. Further USP14 is expressed along with the marker of proliferation Ki67 in endometrial cancer cells in situ. Lastly, pharmacological targeting of USP14 with the FDA approved small-molecule inhibitor VLX1570, decreases cell viability in chemotherapy resistant endometrial cancer cells with a mechanism consistent with cell cycle arrest and caspase-3 mediated apoptosis.

Indexed as

AgedAzepinesBenzylidene CompoundsBiomarkers, TumorCarboplatinCell Line, TumorCell ProliferationCell SurvivalDrug Resistance, NeoplasmEndometrial NeoplasmsEnzyme InhibitorsFemaleHumansMiddle AgedMolecular Targeted TherapyNeoplasm Recurrence, LocalAzepinesBenzylidene CompoundsBiomarkers, TumorCarboplatinEnzyme InhibitorsUbiquitin ThiolesteraseUSP14 protein, humanVLX1570biomarkerendometrial cancerrecurrenceUSP14VLX1570

Identifiers

PMID27121063
PMCPMC5058731
OpenAlexW2338844696

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.