Evidence map›Paper›PMID 32912025›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2020

The intensification of anticancer activity of LFM-A13 by erythropoietin as a possible option for inhibition of breast cancer.

Dariusz Rozkiewicz, Justyna Magdalena Hermanowicz, Anna Tankiewicz-Kwedlo, Beata Sieklucka, Krystyna Pawlak, Robert Czarnomysy, Krzysztof Bielawski, Arkadiusz Surazynski, Joanna Kalafut, Alicja Przybyszewska and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

7 citing papers in PubMed, 5 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

14 authors at 2 institutions in 1 country.

Dariusz RozkiewiczDepartment of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland.
Justyna Magdalena HermanowiczDepartment of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland.
Anna Tankiewicz-KwedloDepartment of Monitored Pharmacotherapy, Medical University of Bialystok, Bialystok, Poland.
Beata SiekluckaDepartment of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland.
Krystyna PawlakDepartment of Monitored Pharmacotherapy, Medical University of Bialystok, Bialystok, Poland.
Robert CzarnomysyDepartment of Synthesis and Technology of Drugs, Medical University of Bialystok, Bialystok, Poland.
Krzysztof BielawskiDepartment of Synthesis and Technology of Drugs, Medical University of Bialystok, Bialystok, Poland.ORCID https://orcid.org/0000-0003-3187-4205
Arkadiusz SurazynskiDepartment of Medicinal Chemistry, Medical University of Bialystok, Bialystok, Poland.
Joanna KalafutDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Alicja PrzybyszewskaDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Mariusz KodaDepartment of General Pathomorphology, Medical University of Bialystok, Bialystok, Poland.
Katarzyna JakubowskaDepartment of Pathomorphology, Comprehensive Cancer Center, Bialystok, Poland.
Adolfo Rivero-MullerDepartment of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
Dariusz PawlakDepartment of Pharmacodynamics, Medical University of Bialystok, Bialystok, Poland.
Medical University of Białystok · PLMedical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recombinant human erythropoietin (Epo) is an effective and convenient treatment for cancer-related anaemia. In our study for the first time, we evaluated the effect of simultaneous use of Epo and Bruton's tyrosine kinase (BTK) inhibitor LFM-A13 on the viability and tumour development of breast cancer cells. The results demonstrated that Epo significantly intensifies the anticancer activity of LFM-A13 in MCF-7 and MDA-MB-231. The featured therapeutic scheme efficiently blocked the tumour development in zebrafish experimental cancer model. Epo and LFM-A13 administered together resulted in effective cell killing, accompanied by attenuation of the BTK signalling pathways, loss of mitochondrial membrane potential (MMP), accumulation of apoptotic breast cancer cells with externalised PS, a slight increase in phase G0/G1 and a reduction in cyclin D1 expression. Simultaneous use of Epo with LFM-A13 inhibited early stages of tumour progression. This therapeutic scheme may be rationale for further possible research.

Indexed as

AdultAgedAged, 80 and overAmidesAntineoplastic AgentsBreast NeoplasmsCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorErythropoietinFemaleHumansMiddle AgedMolecular StructureNitrilesAmidesAntineoplastic AgentsErythropoietinLFM A13Nitrilesbreast cancerBruton’s tyrosine kinaseErythropoietinLFM-A13zebrafish

Identifiers

PMID32912025
PMCPMC7717683
OpenAlexW3085924934

What OpenQuestion holds

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LicenceCC BY
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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.