Evidence map›Paper›PMID 28960447›Full record

ArticleJournal of veterinary internal medicine2017

JAK1/2 Inhibitors AZD1480 and CYT387 Inhibit Canine B-Cell Lymphoma Growth by Increasing Apoptosis and Disrupting Cell Proliferation.

Z Lu, C C Hong, P C Jark, A L F V Assumpção, N Bollig, G Kong, X Pan

Open access · goldAbstract read
In one paragraph

Article in Journal of veterinary internal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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    Review
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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 2 institutions in 3 countries.

Z LuDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
C C HongDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
P C JarkDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
A L F V AssumpçãoDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
N BolligDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
G KongNational Local Joint Engineering Research Center of Biodiagnostics and Biotherapy, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
X PanDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.ORCID http://orcid.org/0000-0002-8308-8495
University of Wisconsin–Madison · USSecond Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

Short-Term Research Training of Veterinary Students in WisconsinT35OD011078 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI BJORLING, DALE EDMOND, JORGENSEN, JOAN S · 2012 to 2025
$1.0M
PcG protein YY1 functions in HSC self-renewal and differentiationK01OD020153 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI PAN, XUAN · 2015 to 2019
$657k
NIH HHS K01 OD020153NIH HHS T35 OD011078
6 · The paper itself

Abstract

backgroundCanine diffuse large B-cell lymphoma (DLBCL) is a common and aggressive hematologic malignancy. The lack of conventional therapies with sustainable efficacy warrants further investigation of novel therapeutics. The Janus kinase (JAK) and signal transducer and activator of transcription (STAT) pathways play important roles in the pathogenesis of hematologic malignancies in humans including DLBCLs. AZD1480 and CYT387 are novel JAK1/2 inhibitors that have been used in clinical trials for treating various hematologic cancers in humans. No studies have characterized the antitumor effects of JAK inhibitors on DLBCL in dogs. HYPOTHESIS/

objectivesWe hypothesize that JAK1/2 inhibitors AZD1480 and CYT387 can effectively inhibit growth of canine DLBCL in vitro. We aim to assess the antitumor activity of AZD1480 and CYT387 in canine DLBCL and to determine the underlying mechanisms of action.

methodsIn vitro study of canine lymphoma cell growth, proliferation, and apoptosis by viability, proliferation and apoptosis assays.

resultsA significant decrease in viable canine lymphoma cells was observed after AZD1480 and CYT387 treatments. In addition, AZD1480 and CYT387 treatment resulted in decreased lymphoma cell proliferation and increased early apoptosis. CONCLUSION AND CLINICAL IMPORTANCE: AZD1480 and CYT387 inhibit canine lymphoma cell growth in a dose-dependent manner. Our findings justify further phase I/II clinical investigations of the safety and efficacy of JAK1/2 inhibitors in canine DLBCL and suggest new opportunities for novel anticancer therapies.

Indexed as

AnimalsApoptosisBenzamidesCell ProliferationDog DiseasesDogsJanus Kinase 1Janus Kinase 2Lymphoma, B-CellProtein Kinase InhibitorsPyrazolesPyrimidinesSTAT Transcription FactorsTumor Cells, CulturedAZD 1480BenzamidesJanus Kinase 1Janus Kinase 2N-(cyanomethyl)-4-(2-((4-(4-morpholinyl)phenyl)amino)-4-pyrimidinyl)benzamideProtein Kinase InhibitorsPyrazolesPyrimidinesSTAT Transcription FactorsApoptosisCanine DLBCLsCell cycleJAK inhibitors

Identifiers

PMID28960447
PMCPMC5697192
OpenAlexW2757063393

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.