动着质体疾病:对药物作用机制和新药物发现的耐药性的见解

Abdullah M. Tauheed , Ammar U. Danazumi , Oluwafemi A. Adepoju , Patricia I. Kobo , Auwal Adamu , Emmanuel O. Balogun
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引用次数: 0

摘要

锥虫和利什曼原虫是动着质体原生动物寄生虫,在发展中国家造成严重的残疾调整生命年(DALYs)和农业损失。尽管在了解这些被忽视疾病病原体的生物学和化疗方面取得了进展,但由于耐药性或毒性驱动的不依从性导致的治疗失败仍然是主要挑战。分子寄生虫学的进步已经导致了特定的运输机制,可药物靶点和持续细胞的鉴定,它们在治疗的整体成功中起着独特的作用。转运蛋白和其他细胞转运机制影响药物的内化及其细胞内可用性,从而决定药物活性。因此,我们回顾了着丝体药物转运机制,分子药物靶点和持续物,以突出抗着丝体药物的作用机制和耐药性的发展,旨在为药物发现计划提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kinetoplastid diseases: Insights into the mechanisms of drug action and resistance for novel drug discovery
Trypanosoma and Leishmania species are kinetoplastid protozoan parasites that cause diseases which result in significant disability-adjusted life years (DALYs) and agricultural losses in the developing world. Despite the progress recorded in understanding biology and chemotherapy of these pathogens of neglected diseases, treatment failure, due to drug resistance or toxicity-driven non-compliance remain major challenges. Advances in molecular parasitology have led to the identification of specific transport mechanisms, druggable targets and persister-like cells, which play distinct roles in the overall success of therapies. Transporters and other cellular transport mechanisms affect the internalisation of drugs and their intracellular availability which determine drug activity. Thus, we reviewed kinetoplastid drug transport mechanisms, molecular drug targets and persisters to highlight mechanisms of action and development of resistance for antikinetoplastid drugs, with the aim of providing novel insights for drug discovery programmes.
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来源期刊
Aspects of molecular medicine
Aspects of molecular medicine Molecular Biology, Molecular Medicine
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