Seki Kioshima Erika, de Souza Bonfim de Mendonça Patrícia, de Melo Teixeira Marcus, Grenier Capoci Isis Regina, Amaral André, Vilugron Rodrigues-Vendramini Franciele Abigail, Lauton Simões Bruna, Rodrigues Abadio Ana Karina, Fernandes Matos Larissa, Soares Felipe Maria Sueli
Program in Biosciences and Pathophysiology, Department of Clinical Analysis and Biomedicine, State University of Maringa (UEM), Maringa, Parana 87020-900, Brazil.
Faculty of Medicine, University of Brasília (UnB), Brasilia, Distrito Federal 70910-900, Brazil.
J Fungi (Basel). 2021 Feb 2;7(2):106. doi: 10.3390/jof7020106.
Paracoccidioidomycosis (PCM) is a notable fungal infection restricted to Latin America. Since the first description of the disease by Lutz up to the present day, Brazilian researchers have contributed to the understanding of the life cycle of this pathogen and provided the possibility of new targets for antifungal therapy based on the structural and functional genomics of . In this context, approaches have selected molecules that act on specific targets, such as the thioredoxin system, with promising antifungal activity against . Some of these are already in advanced development stages. In addition, the application of nanostructured systems has addressed issues related to the high toxicity of conventional PCM therapy. Thus, the contribution of molecular biology and biotechnology to the advances achieved is unquestionable. However, it is still necessary to transcend the boundaries of synthetic chemistry, pharmaco-technics, and pharmacodynamics, aiming to turn promising molecules into newly available drugs for the treatment of fungal diseases.
副球孢子菌病(PCM)是一种仅限于拉丁美洲的显著真菌感染。自卢茨首次描述该疾病至今,巴西研究人员为了解这种病原体的生命周期做出了贡献,并基于其结构和功能基因组学为抗真菌治疗提供了新靶点的可能性。在此背景下,一些方法已筛选出作用于特定靶点(如硫氧还蛋白系统)的分子,这些分子对[此处原文缺失相关内容]具有有前景的抗真菌活性。其中一些已处于 advanced development stages(此处可能有误,推测为advanced development phases,即“高级开发阶段”)。此外,纳米结构系统的应用解决了与传统PCM治疗高毒性相关的问题。因此,分子生物学和生物技术对所取得进展的贡献是毋庸置疑的。然而,仍有必要超越合成化学、药物技术和药效学的界限,旨在将有前景的分子转化为治疗真菌疾病的新可用药物。