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为抗真菌药物研发开辟新途径以对抗致病真菌。

Setting New Routes for Antifungal Drug Discovery Against Pathogenic Fungi.

机构信息

Laboratório de Biologia Molecular, Instituto de Ciências Biológicas, Universidade Federal de Goiás, Goiânia, Brazil.

LabMol - Laboratory for Molecular Modeling and Drug Design, Faculdade de Farmácia, Universidade Federal de Goiás, Goiânia, GO, 74605-510, Brazil.

出版信息

Curr Pharm Des. 2020;26(14):1509-1520. doi: 10.2174/1381612826666200317125956.

Abstract

Fungal diseases are life-threatening to human health and responsible for millions of deaths around the world. Fungal pathogens lead to a high number of morbidity and mortality. Current antifungal treatment comprises drugs, such as azoles, echinocandins, and polyenes and the cure is not guaranteed. In addition, such drugs are related to severe side effects and the treatment lasts for an extended period. Thus, setting new routes for the discovery of effective and safe antifungal drugs should be a priority within the health care system. The discovery of alternative and efficient antifungal drugs showing fewer side effects is time-consuming and remains a challenge. Natural products can be a source of antifungals and used in combinatorial therapy. The most important natural products are antifungal peptides, antifungal lectins, antifungal plants, and fungi secondary metabolites. Several proteins, enzymes, and metabolic pathways could be targets for the discovery of efficient inhibitor compounds and recently, heat shock proteins, calcineurin, salinomycin, the trehalose biosynthetic pathway, and the glyoxylate cycle have been investigated in several fungal species. HSP protein inhibitors and echinocandins have been shown to have a fungicidal effect against azole-resistant fungi strains. Transcriptomic and proteomic approaches have advanced antifungal drug discovery and pointed to new important specific-pathogen targets. Certain enzymes, such as those from the glyoxylate cycle, have been a target of antifungal compounds in several fungi species. Natural and synthetic compounds inhibited the activity of such enzymes and reduced the ability of fungal cells to transit from mycelium to yeast, proving to be promisor antifungal agents. Finally, computational biology has developed effective approaches, setting new routes for early antifungal drug discovery since normal approaches take several years from discovery to clinical use. Thus, the development of new antifungal strategies might reduce the therapeutic time and increase the quality of life of patients.

摘要

真菌病对人类健康构成严重威胁,是导致全球数百万人死亡的原因之一。真菌病原体导致大量发病率和死亡率。目前的抗真菌治疗包括药物,如唑类、棘白菌素和多烯类,且治疗效果无法保证。此外,这些药物与严重的副作用有关,治疗时间较长。因此,在医疗保健系统中,应该优先寻找新的方法来发现有效和安全的抗真菌药物。发现具有较少副作用的替代和有效的抗真菌药物是一个耗时的过程,仍然是一个挑战。天然产物可以成为抗真菌药物的来源,并用于联合治疗。最重要的天然产物是抗真菌肽、抗真菌凝集素、抗真菌植物和真菌次级代谢产物。几种蛋白质、酶和代谢途径可能成为发现有效抑制剂化合物的目标,最近,热休克蛋白、钙调神经磷酸酶、盐霉素、海藻糖生物合成途径和乙醛酸循环已在几种真菌物种中进行了研究。HSP 蛋白抑制剂和棘白菌素已被证明对唑类耐药真菌菌株具有杀菌作用。转录组学和蛋白质组学方法促进了抗真菌药物的发现,并指出了新的重要特定病原体靶标。某些酶,如乙醛酸循环中的酶,已成为几种真菌物种中抗真菌化合物的靶标。天然和合成化合物抑制了这些酶的活性,降低了真菌细胞从菌丝体向酵母转化的能力,证明是很有前途的抗真菌剂。最后,计算生物学已经开发出有效的方法,为早期抗真菌药物发现开辟了新的途径,因为从发现到临床应用通常需要数年时间。因此,开发新的抗真菌策略可能会缩短治疗时间,提高患者的生活质量。

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