Evidence map›Paper›PMID 32365663›Full record

ArticleCancers2020

Celecoxib Prevents Doxorubicin-Induced Multidrug Resistance in Canine and Mouse Lymphoma Cell Lines.

Edina Karai, Kornélia Szebényi, Tímea Windt, Sára Fehér, Eszter Szendi, Valéria Dékay, Péter Vajdovich, Gergely Szakács, András Füredi

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 16 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

9 authors at 2 institutions in 2 countries.

Edina KaraiInstitute of Enzymology, Research Centre of Natural Sciences, Eötvös Loránd Research Network, Magyar Tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0002-8432-9668
Kornélia SzebényiInstitute of Enzymology, Research Centre of Natural Sciences, Eötvös Loránd Research Network, Magyar Tudósok körútja 2, H-1117 Budapest, Hungary.
Tímea WindtInstitute of Enzymology, Research Centre of Natural Sciences, Eötvös Loránd Research Network, Magyar Tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0001-9913-3337
Sára FehérDepartment of Clinical Pathology and Oncology, University of Veterinary Medicine Budapest, István utca 2, H-1078 Budapest, Hungary.
Eszter SzendiDepartment of Clinical Pathology and Oncology, University of Veterinary Medicine Budapest, István utca 2, H-1078 Budapest, Hungary.
Valéria DékayDepartment of Clinical Pathology and Oncology, University of Veterinary Medicine Budapest, István utca 2, H-1078 Budapest, Hungary.
Péter VajdovichDepartment of Clinical Pathology and Oncology, University of Veterinary Medicine Budapest, István utca 2, H-1078 Budapest, Hungary.
Gergely SzakácsInstitute of Enzymology, Research Centre of Natural Sciences, Eötvös Loránd Research Network, Magyar Tudósok körútja 2, H-1117 Budapest, Hungary.
András FürediInstitute of Enzymology, Research Centre of Natural Sciences, Eötvös Loránd Research Network, Magyar Tudósok körútja 2, H-1117 Budapest, Hungary.ORCID 0000-0002-7883-9901
University of Veterinary Medicine · HUInstitute of Molecular Life Sciences · HU

Funding

Magyar Tudományos Akadémia Momentum GrantNemzeti Kutatási Fejlesztési és Innovációs Hivatal 2019-1.3.1-KK-2019-00007
6 · The paper itself

Abstract

backgroundTreatment of malignancies is still a major challenge in human and canine cancer, mostly due to the emergence of multidrug resistance (MDR). One of the main contributors of MDR is the overexpression P-glycoprotein (Pgp), which recognizes and extrudes various chemotherapeutics from cancer cells.

methodsTo study mechanisms underlying the development of drug resistance, we established an in vitro treatment protocol to rapidly induce Pgp-mediated MDR in cancer cells. Based on a clinical observation showing that a 33-day-long, unplanned drug holiday can reverse the MDR phenotype of a canine diffuse large B-cell lymphoma patient, our aim was to use the established assay to prevent the emergence of drug resistance in the early stages of treatment.

resultsWe showed that an in vitro drug holiday results in the decrease of Pgp expression in MDR cell lines. Surprisingly, celecoxib, a known COX-2 inhibitor, prevented the emergence of drug-induced MDR in murine and canine lymphoma cell lines.

conclusionsOur findings suggest that celecoxib could significantly improve the efficiency of chemotherapy by preventing the development of MDR in B-cell lymphoma.

Indexed as

celecoxibCOX-2 inhibitorsdrug holidaylymphomamultidrug resistanceP-glycoprotein

Identifiers

PMID32365663
PMCPMC7280963
OpenAlexW3021954955

What OpenQuestion holds

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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.