含酚类化合物的抗癌杂交组合

Eva María Domínguez Martín, A. M. D. Lanza, P. Rijo, C. Faustino
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引用次数: 0

摘要

癌症的特点是细胞生长异常,包括不受控制的细胞分裂,目前正在采用不同的治疗方法来治疗癌症。然而,它们通常缺乏选择性和耐药性的发展导致治疗效果有限或无效。由于这些原因,为这种疾病寻求新的治疗方案是必要的。目前,一些次生代谢物如多酚的生物活性特性已被公认,这使得抗肿瘤杂交组合成为一种很有前途的治疗方法。本文旨在对含酚类化合物的抗癌杂交组合进行综述,重点介绍其多靶点作用机制和协同效应。这些组合由合成药物与植物化学成分(次生代谢物,在这种情况下,酚类化合物)的治疗性混合物组成,旨在增加制剂的药理活性,同时减少药物的毒副作用,称为协同作用。抗肿瘤杂交组合是一种很有前途的治疗策略,可以最大限度地减少不良反应,降低癌症对不同治疗的耐药性。同时,它显示出对肿瘤细胞的选择性,增强了药物的活性,使其成为治疗癌症的有趣选择。参考文献:[1]Dominguez-Martin EM, Diaz-Lanza AM, Faustino CMC(2018)现代药学杂志,24,4312-4333.[2]王晓明,王晓明,王晓明(2017)植物医学,32 (5):481 - 481 .[j]引用本文Mahbub AA, Le Maitre CL, Haywood-Small S, Cross NA, Nicola Jordan-Mahy N(2019)肿瘤防治靶标10,4570-86[J]钟超,李军,沈军,祖勇,史军,隋刚(2019)植物医学59,152921
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticancer Hybrid Combinations with phenolic compounds
Different types of treatments are being employed to overcome cancer, which is characterized by abnormal cell growth involving cell division without control. However, their usually lack of selectivity and the development of resistance result in limited efficacy or ineffectiveness of the therapies. For these reasons, seeking new treatment options for this disease is necessary. Nowadays, the acknowledge bioactive properties of some secondary metabolites such as polyphenols, have made antitumour hybrid combinations a promising therapeutic approach. This work aims to provide a synopsis into Anticancer Hybrid Combinations involving phenolic compounds, focusing on their multi-target mechanisms of action and synergistic effects. These combinations consist on the therapeutic mixture of synthetic drugs with chemically defined constituents from plants (secondary metabolites, in this case, phenolic compounds) aiming to increase the pharmacological activity of the formulation and simultaneously reduce the toxic side-effects of the drugs, interaction known as synergy. Antitumour hybrid combinations are a promising therapeutic strategy to minimize adverse effects and to reduce cancer resistance to different treatments. At the same time, it shows selectivity to tumour cells and potentiate the activity of the drug that make them an interesting option to cure cancer. References: [1] Dominguez-Martin EM, Diaz-Lanza AM, Faustino CMC (2018) Curr Pharm Des 24, 4312-4333.[2] Wagner H, Efferth T. (2017) Phytomedicine, 37, 1-3.[3] Mahbub AA, Le Maitre CL, Haywood-Small S, Cross NA, Nicola Jordan-Mahy N (2019) Oncotarget 10, 4570-86[4] Zhong C, Qiu S, Li J, Shen J, Zu Y, Shi J, Sui G (2019) Phytomedicine 59, 152921
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