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聚焦Cdr1:对多药转运蛋白研究的个人反思

Cdr1 in focus: a personal reflection on multidrug transporter research.

作者信息

Prasad Rajendra

机构信息

Amity Institute of Integrative Science and Health, Amity University Haryana, Gurugram, 122413, India.

Amity Institute of Biotechnology, Amity University Haryana, Gurugram, 122413, India.

出版信息

FEMS Yeast Res. 2025 Jan 30;25. doi: 10.1093/femsyr/foaf003.

Abstract

Drug resistance mechanisms in human pathogenic Candida species are constantly evolving. Over time, these species have developed diverse strategies to counter the effects of various drug classes, making them a significant threat to human health. In addition to well-known mechanisms such as drug target modification, overexpression, and chromosome duplication, Candida species have also developed permeability barriers to antifungal drugs through reduced drug import or increased efflux. The genomes of Candida species contain a multitude of drug resistance genes, many of which encode membrane efflux transporters that actively expel drugs, preventing their toxic accumulation inside the cells and contributing to multidrug resistance. This brief personal retrospective piece for the "Thematic Issue on Celebrating 30 Years of Cdr1 Research: new trends in antifungal therapy and drug resistance" looks back as to how antifungal research has shifted focus since the identification of the first multidrug transporter gene, CDR1 (Candida Drug Resistance 1), leading to new insights into how reduced azole permeability across Candida cell membranes influences antifungal susceptibility.

摘要

人类致病念珠菌属的耐药机制在不断演变。随着时间的推移,这些菌种已发展出多种策略来对抗各类药物的作用,对人类健康构成了重大威胁。除了药物靶点修饰、过表达和染色体复制等众所周知的机制外,念珠菌属还通过减少药物摄入或增加外排,形成了对抗真菌药物的通透性屏障。念珠菌属的基因组包含大量耐药基因,其中许多编码膜外排转运蛋白,这些蛋白可主动排出药物,防止其在细胞内的毒性积累,并导致多重耐药。这篇为“庆祝Cdr1研究30周年专题:抗真菌治疗与耐药性的新趋势”撰写的简短个人回顾文章,回顾了自首个多重耐药转运蛋白基因CDR1(念珠菌耐药1)被鉴定以来,抗真菌研究重点是如何转变的,从而对念珠菌细胞膜上唑类通透性降低如何影响抗真菌药敏性有了新的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c067/11781190/a19229cdefcb/foaf003fig1.jpg

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