Evidence map›Paper›PMID 30101447›Full record

ArticleVeterinary and comparative oncology2018

Targeting NEDD8-activating enzyme is a new approach to treat canine diffuse large B-cell lymphoma.

A L F V Assumpção, Z Lu, K W Marlowe, K S Shaffer, X Pan

Abstract read
In one paragraph

Article in Veterinary and comparative oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. 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

5 authors at 1 institution in 1 country.

A L F V AssumpçãoDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
Z LuDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
K W MarloweDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
K S ShafferDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.
X PanDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, Wisconsin.ORCID https://orcid.org/0000-0002-8308-8495
University of Wisconsin–Madison · US

Funding

Mechanisms that Regulate Self-renewal and Proliferation in Hematopoietic Stem CellsR01HL146540 · NHLBI · UNIVERSITY OF WISCONSIN-MADISON · PI PAN, XUAN · 2019 to 2023
$1.9M
PcG protein YY1 functions in HSC self-renewal and differentiationK01OD020153 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI PAN, XUAN · 2015 to 2019
$657k
Molecular Mechanisms of Hematopoietic Stem Cell DevelopmentR03OD026603 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI PAN, XUAN · 2019 to 2020
$230k
Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorNHLBI NIH HHS R01 HL146540NIH HHS K01 OD020153NIH HHS R03 OD026603NIH Office of the Director K01OD020153-01A1University of Wisconsin-Madison Companion Animal Fund
6 · The paper itself

Abstract

Canine diffuse large B-cell lymphoma (DLBCL), the most common hematologic malignancy of dogs, is associated with poor overall survival. The lack of conventional chemotherapies with sustainable efficacy warrants investigation of novel therapies. Pevonedistat (MLN4924) is a potent and selective small molecule NEDD8-activating enzyme inhibitor. In human activated B-cell-like (ABC) diffuse large B-cell lymphoma, pevonedistat induces lymphoma cell apoptosis, DNA damage and G1 cell cycle arrest by inhibiting the nuclear factor-κB (NF-κB) pathway. Genomic and transcriptomic studies showed that the NF-κB pathway is deregulated in canine DLBCL. Our results showed that pevonedistat treatment significantly reduces the viability of canine DLBCL cells by inducing G1 cell cycle arrest and apoptosis. Pevonedistat treatment inhibits NF-κB pathway activation and downregulates NF-κB target genes in canine DLBCL. Moreover, administration of pevonedistat to mice bearing canine DLBCL xenograft tumours resulted in tumour regression. Our in vivo and in vitro studies provide justification for future clinical application of pevonedistat as a potential new anti-cancer therapy that may benefit both canine and human species.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBlotting, WesternCell Line, TumorCell ProliferationCyclopentanesDog DiseasesDogsDose-Response Relationship, DrugInhibitory Concentration 50Lymphoma, Large B-Cell, DiffuseMiceMice, Inbred NODNEDD8 ProteinNeoplasm TransplantationAntineoplastic AgentsCyclopentanesNEDD8 ProteinpevonedistatPyrimidinesUbiquitin-Activating EnzymescanineDLBCLNAE-inhibitorNF-κB pathwayxenograft tumour

Identifiers

PMID30101447
PMCPMC6392197
OpenAlexW2886448606

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.