Evidence map›Paper›PMID 36825727›Full record

ArticleRecent patents on anti-cancer drug discovery2025

Preclinical Effects of Melatonin on the Development of Ehrlich's Tumor: A Biochemical, Cognitive, and Molecular Approach.

Ivan Pereira Lopes, Bianca Souza Bagatela, Andrey Pereira Lopes, Elaine Ferreira Silveira, Giuliana Petri, Jose Francisco Ramos Santos, Matheus Moreira Perez, Glaucia Luciano da Veiga, Beatriz da Costa Aguiar Alves, Fabio Ferreira Perazzo and 2 more

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Article in Recent patents on anti-cancer drug discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

12 authors at 4 institutions in 1 country.

Ivan Pereira LopesLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Bianca Souza BagatelaLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Andrey Pereira LopesLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.ORCID 0000-0002-1721-3374
Elaine Ferreira SilveiraFaculdade de Medicina, Universidade Anhembi Morumbi (UAM), São Paulo, SP, Brazil.ORCID 0000-0003-2920-2653
Giuliana PetriLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.ORCID 0000-0002-6078-9184
Jose Francisco Ramos SantosLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Matheus Moreira PerezLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Glaucia Luciano da VeigaLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Beatriz da Costa Aguiar AlvesLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Fabio Ferreira PerazzoDepartamento de Ciências Farmacêuticas, Universidade Federal de São Paulo (UNIFESP), Diadema, SP, Brazil.
David FederLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Fernando Luiz Affonso FonsecaLaboratório de Análises Clínicas do Centro, Universitário FMABC, Santo André, SP, Brazil.
Faculdade de Medicina do ABC · BRAnhembi Morumbi University · BRInstituto de Ciências Farmacêuticas · BRUniversidade Federal de São Paulo · BR

Funding

FAPESP, Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/19301-4
6 · The paper itself

Abstract

backgroundIt has already been shown that melatonin is an antitumoral molecule that affects malignant cells via some mechanisms. The benefit played by this hormone on cancer is due to its antioxidant effects.

objectiveThis study aimed to evaluate the preclinical effects of melatonin in mice with the Ehrlich ascites tumor.

methodsTwenty Balb/c male mice with Ehrlich tumor were treated with different melatonin doses. Their inflammatory and oxidative stress were accessed by gene expression. Hepatotoxicity and hematological parameters were also evaluated through biochemical analyses. Animal welfare was analysed weekly from the categories guided by the NC3Rs.

resultsGene expression analyses have shown that only Tnfα and Sod1 were expressed in all groups studied. Only the M-3 group showed increased Tnfα expression compared to the control. All groups treated with melatonin showed decreased Sod1 expression compared to the control. No signs of hepatotoxicity were caused by any of the melatonin doses used in the treatment.

conclusionIn animals with Ehrlich´s tumor treated with melatonin, a decrease in oxidative stress, an amelioration in welfare and in cognitive tasks could be observed, even if the treatment has not reduced the size of the tumor itself. In parallel with the already patented use of melatonin in the treatment of sleep disorders or chronic kidney disease, our results propose its use to improve the general well-being of breast cancer patients.

Indexed as

AntioxidantsCarcinoma, Ehrlich TumorCognitionMelatoninAnimalsMaleMiceMice, Inbred BALB COxidative StressSuperoxide Dismutase-1Tumor Necrosis Factor-alphaAntioxidantsMelatoninSuperoxide Dismutase-1Tumor Necrosis Factor-alphacognitionehrlich’s tumorhepatotoxicity.Melatoninneoplasiapre-clinical

Identifiers

PMID36825727
OpenAlexW4321748992

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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.