Mechanisms Involved in the Therapeutic Effect of Cannabinoid Compounds on Gliomas: A Review with Experimental Approach

胶质瘤 对接(动物) 大麻素受体 药理学 体内 背景(考古学) 大麻素 生物 化学 计算生物学 癌症研究 医学 受体 生物化学 护理部 兴奋剂 古生物学 生物技术
作者
Hugo Fernandes Oliveira Pires,Pablo Rayff da Silva,Arthur Lins Dias,Cleyton de Sousa Gomes,Natália Ferreira de Sousa,Aline Matilde Ferreira dos Santos,Lívia Roberta Pimenta Souza,Jaislânia Lucena de Figueiredo Lima,Mayara Cecile Nascimento Oliveira,Cícero Francisco Bezerra Felipe,Reinaldo Nóbrega de Almeida,Ricardo Dias de Castro,Mirian Graciela da Silva Stiebbe Salvadori,Luciana Scotti,Luciana Scotti
出处
期刊:Current Protein & Peptide Science [Bentham Science Publishers]
卷期号:25 (1): 27-43 被引量:1
标识
DOI:10.2174/1389203724666230830125423
摘要

Introduction: Brain tumors have high morbidity and mortality rates, accounting for 1.4% of all cancers. Gliomas are the most common primary brain tumors in adults. Currently, several therapeutic approaches are used; however, they are associated with side effects that affect patients’quality of life. Therefore, further studies are needed to develop novel therapeutic protocols with a more favorable side effect profile. In this context, cannabinoid compounds may serve as potential alternatives. Objective: This study aimed to review the key enzymatic targets involved in glioma pathophysiology and evaluate the potential interaction of these targets with four cannabinoid derivatives through molecular docking simulations. Methods: Molecular docking simulations were performed using four cannabinoid compounds and six molecular targets associated with glioma pathophysiology. Results: Encouraging interactions between the selected enzymes and glioma-related targets were observed, suggesting their potential activity through these pathways. In particular, cannabigerol showed promising interactions with epidermal growth factor receptors and phosphatidylinositol 3- kinase, while Δ-9-tetrahydrocannabinol showed remarkable interactions with telomerase reverse transcriptase. Conclusion: The evaluated compounds exhibited favorable interactions with the analyzed enzymatic targets, thus representing potential candidates for further in vitro and in vivo studies.

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