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Phthalides Isolated from the Endolichenic Arthrinium sp. EL000127 Exhibits Antiangiogenic Activityopen access

Authors
Gamage, Chathurika D. B.Lee, KyunghaPark, So-YeonVarli, MücahitLee, Chang WookKim, Seong-MinZhou, RuiPulat, SultanYang, YiTaş, İsaHur, Jae-SeounKang, Kyo BinKim, Hangun
Issue Date
Mar-2023
Publisher
American Chemical Society
Citation
ACS Omega, v.8, no.13, pp 12548 - 12557
Pages
10
Journal Title
ACS Omega
Volume
8
Number
13
Start Page
12548
End Page
12557
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/159485
DOI
10.1021/acsomega.3c00876
ISSN
2470-1343
Abstract
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 Arthrinium 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-O-methylcyclopolic acid (1), and two unknown analogues of 1, 3-O-phenylethylcyclopolic acid (2) and 3-O-p-hydroxyphenylethylcyclopolic acid (3). 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 3 effectively inhibits HUVEC motility by suppressing mRNA expressions of genes regulating epithelial cell survival and motility, which suggested that compound 3 is a potent antiangiogenic agent suitable for further exploration as a potential novel therapeutic against cancers. © 2023 The Authors. Published by American Chemical Society
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