Gamage Chathurika D B, Lee Kyungha, Park So-Yeon, Varlı Mücahit, Lee Chang Wook, Kim Seong-Min, Zhou Rui, Pulat Sultan, Yang Yi, Taş İsa, Hur Jae-Seoun, Kang Kyo Bin, Kim Hangun
College of Pharmacy, Sunchon National University, 255 Jungang-ro, Sunchon, Jeonnam 57922, Korea.
Research Institute of Pharmaceutical Sciences, College of Pharmacy, Sookmyung Women's University, 100 Cheongpa-ro 47 gil, Seoul 04310, Korea.
ACS Omega. 2023 Mar 21;8(13):12548-12557. doi: 10.1021/acsomega.3c00876. eCollection 2023 Apr 4.
Endolichenic fungi (ELF) produce specialized metabolites that have various medicinal properties. Inhibition of tumor angiogenesis efficaciously suppresses many types of cancer. This study aimed to discover novel antiangiogenic agents from specialized metabolite extracts of ELF strains isolated from Korean lichens. The EtOAc extracts of 51 ELF strains were subjected to a screening pipeline consisting of cell viability, scratch wound healing, and Transwell migration assays. The EtOAc extract of sp. EL000127 showed the most potent inhibitory activity against the chemotactic migration of human umbilical vein endothelial cells (HUVEC). Targeted isolation on the major LC-MS peaks exhibited a previously known phthalide, 3--methylcyclopolic acid (), and two unknown analogues of , 3--phenylethylcyclopolic acid () and 3---hydroxyphenylethylcyclopolic acid (). The structures were characterized by MS and NMR analyses. All the isolates were acquired and applied to bioassays as racemates due to spontaneous racemization. Among the isolates, compound effectively inhibits HUVEC motility by suppressing mRNA expressions of genes regulating epithelial cell survival and motility, which suggested that compound is a potent antiangiogenic agent suitable for further exploration as a potential novel therapeutic against cancers.
内生地衣真菌(ELF)能产生具有多种药用特性的特殊代谢产物。抑制肿瘤血管生成可有效抑制多种类型的癌症。本研究旨在从从韩国地衣中分离出的ELF菌株的特殊代谢产物提取物中发现新型抗血管生成剂。对51株ELF菌株的乙酸乙酯提取物进行了包括细胞活力、划痕伤口愈合和Transwell迁移试验在内的筛选流程。菌株EL000127的乙酸乙酯提取物对人脐静脉内皮细胞(HUVEC)的趋化迁移表现出最有效的抑制活性。对主要液相色谱 - 质谱峰进行靶向分离,得到一种已知的苯酞、3 - 甲基环珀酸(),以及两种未知的类似物,3 - 苯乙基环珀酸()和3 - ( - 羟基苯乙基)环珀酸()。通过质谱和核磁共振分析对其结构进行了表征。由于自发外消旋作用,所有分离物均以外消旋体形式获得并应用于生物测定。在这些分离物中,化合物 通过抑制调节上皮细胞存活和运动的基因的mRNA表达,有效抑制了HUVEC的运动,这表明化合物 是一种有效的抗血管生成剂,适合作为一种潜在的新型癌症治疗药物进行进一步探索。