Preclinical Effects Of Melatonin On The Development Of Ehrlich's Tumor: A Biochemical, Cognitive, And Molecular Approach.

IF 2.5 4区 医学 Q3 ONCOLOGY
Ivan Pereira Lopes, Bianca Souza Bagatela, Andrey Pereira Lopes, Elaine Ferreira Silveira, Giuliana Petri, José Francisco Ramos Santos, Matheus Moreira Perez, Glaucia Luciano da Veiga, Beatriz da Costa Aguiar Alves, Fábio Ferreira Perazzo, David Feder, Fernando Luiz Affonso Fonseca
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引用次数: 0

Abstract

Background: It 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.

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

Methods: Twenty 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.

Results: Gene 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.

Conclusion: In 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.

褪黑激素对艾氏肿瘤发生的临床前影响:生化、认知和分子方法。
背景:已有研究表明,褪黑激素是一种抗肿瘤分子,可通过某些机制影响恶性细胞。这种激素对癌症的益处在于其抗氧化作用:本研究旨在评估褪黑激素对艾氏腹水瘤小鼠的临床前效应:方法:用不同剂量的褪黑激素治疗20只患有艾氏腹水瘤的Balb/ c雄性小鼠。通过基因表达检测小鼠的炎症和氧化应激反应。还通过生化分析评估了肝毒性和血液学参数。每周根据 NC3Rs 的分类对动物福利进行分析:基因表达分析表明,所有研究组中只有 Tnfα 和 Sod1 有表达。与对照组相比,只有 M-3 组的 Tnfα 表达量有所增加。与对照组相比,用褪黑素治疗的所有组都显示出 Sod1 表达下降。任何剂量的褪黑激素治疗均未引起肝中毒症状:在使用褪黑激素治疗艾氏瘤的动物中,可以观察到氧化应激的减少、福利和认知任务的改善,即使治疗并没有减少肿瘤本身的大小。褪黑素在治疗睡眠障碍或慢性肾病方面已经获得了专利,与此同时,我们的研究结果还建议使用褪黑素来改善乳腺癌患者的总体健康状况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.50
自引率
7.10%
发文量
55
审稿时长
3 months
期刊介绍: Aims & Scope Recent Patents on Anti-Cancer Drug Discovery publishes review and research articles that reflect or deal with studies in relation to a patent, application of reported patents in a study, discussion of comparison of results regarding application of a given patent, etc., and also guest edited thematic issues on recent patents in the field of anti-cancer drug discovery e.g. on novel bioactive compounds, analogs, targets & predictive biomarkers & drug efficacy biomarkers. The journal also publishes book reviews of eBooks and books on anti-cancer drug discovery. A selection of important and recent patents on anti-cancer drug discovery is also included in the journal. The journal is essential reading for all researchers involved in anti-cancer drug design and discovery. The journal also covers recent research (where patents have been registered) in fast emerging therapeutic areas/targets & therapeutic agents related to anti-cancer drug discovery.
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