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Setting New Routes for Antifungal Drug Discovery Against Pathogenic Fungi

机译:对致病性真菌进行抗真菌药物发现的新途径

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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 mutes 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.
机译:真菌疾病是生命的威胁人类健康和负责世界各地数百万人死亡。真菌病原体导致大量的发病率和死亡率。当前抗真菌治疗包括药物,如唑类,棘球白素,和多烯和固化不被保证。此外,这类药物都与严重的副作用,治疗持续较长的时间。因此,对于安全有效的抗真菌药物的发现设置新的静音应该是医疗体系内的优先事项。的替代的和有效的抗真菌药物示出较少的副作用的发现是耗时且仍然是一个挑战。天然产品可以抗真菌药物的来源,并在组合疗法。最重要的天然产品是抗真菌肽,抗真菌外源凝集素,抗真菌植物和真菌次生代谢产物。几种蛋白质,酶,和代谢途径可能是有效的抑制剂化合物的发现目标和最近,热休克蛋白,钙调磷酸酶,盐霉素,海藻糖生物合成途径,和乙醛酸循环在几个真菌物种进行了研究。 HSP蛋白抑制剂和棘球白素类已经显示出具有对耐唑的真菌菌株的杀真菌效果。转录和蛋白质组学方法有先进的抗真菌的药物发现和指出了新的重要的具体病原体的目标。某些酶,如那些从乙醛酸循环,已经在几种真菌物种是抗真菌化合物的对象。天然和合成的化合物抑制这些酶的活性和从菌丝减少真菌细胞的能力转变到酵母,证明是允诺抗真菌剂。最后,计算生物学已发展的有效途径,对于早期抗真菌药物的发现设置新的路线,因为正常的方法需要数年时间从发现到临床使用。因此,新的抗真菌药物的发展战略可能会减少治疗时间,提高患者的生活质量。

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