Evidence map›Paper›PMID 27507155›Full record

ArticleVeterinary and comparative oncology2017

IL-4 downregulates expression of the target receptor CD30 in neoplastic canine mast cells.

K Bauer, E Hadzijusufovic, S Cerny-Reiterer, G Hoermann, M Reifinger, A Pirker, P Valent, M Willmann

Open access · greenAbstract read
In one paragraph

Article in Veterinary and comparative oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

K BauerDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
E HadzijusufovicDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
S Cerny-ReitererDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
G HoermannDepartment for Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
M ReifingerDepartment of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
A PirkerDepartment/Clinic for Companion Animals and Horses, Clinic for Small Animals, Clinical Unit of Surgery, University of Veterinary Medicine Vienna, Vienna, Austria.
P ValentDepartment of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
M WillmannDepartment/Clinic for Companion Animals and Horses, Clinic for Small Animals, Clinical Unit of Internal Medicine, University of Veterinary Medicine Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-4260-1491
University of Veterinary Medicine Vienna · ATLudwig Boltzmann Institute for Cardiovascular Research · ATMedical University of Vienna · AT

Funding

Austrian Science Fund FWF F 4704Austrian Science Fund FWF P 21173Austrian Science Fund FWF P 25937
6 · The paper itself

Abstract

CD30 is a novel therapeutic target in human mast cell (MC) neoplasms. In this 'comparative oncology' study, we examined CD30 expression and regulation in neoplastic canine MC using a panel of immunomodulatory cytokines [interleukin-2 (IL-2), IL-4, IL-5, IL-6, IL-13 and stem cell factor (SCF)] and the canine mastocytoma cell lines NI-1 and C2. Of all cytokines tested IL-4 was found to downregulate expression of CD30 in NI-1 and C2 cells. We also found that the CD30-targeting antibody-conjugate brentuximab vedotin induces growth inhibition and apoptosis in both MC lines. Next, we asked whether IL-4-induced downregulation of CD30 interferes with brentuximab vedotin-effects. Indeed, pre-incubation of NI-1 cells with IL-4 decreased responsiveness towards brentuximab vedotin. To overcome IL-4-mediated resistance, we applied drug combinations and found that brentuximab vedotin synergizes with the Kit-targeting drugs masitinib and PKC412 in inhibiting growth of NI-1 and C2 cells. In summary, CD30 is a new marker and IL-4-regulated target in neoplastic canine MC.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBenzamidesBrentuximab VedotinCell Line, TumorCytokinesDog DiseasesDogsDown-RegulationDrug SynergismFemaleImmunoconjugatesInterleukin-4Ki-1 AntigenMaleAntineoplastic AgentsBenzamidesBrentuximab VedotinCytokinesImmunoconjugatesInterleukin-4Ki-1 AntigenmasitinibmidostaurinPiperidinesPyridinesStaurosporineThiazolesbrentuximab vedotincanine mastocytomaCD30IL-4masitinibPKC412

Identifiers

PMID27507155
PMCPMC5798577
OpenAlexW2512598901

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Registered trials

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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.