Two cyclic hexapeptides from Penicillium sp. FN070315 with antiangiogenic activities

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dc.contributor.authorJun-Pil Jang-
dc.contributor.authorH J Jung-
dc.contributor.authorJ M Han-
dc.contributor.authorN Jung-
dc.contributor.authorY Kim-
dc.contributor.authorH J Kwon-
dc.contributor.authorSung-Kyun Ko-
dc.contributor.authorNak Kyun Soung-
dc.contributor.authorJae-Hyuk Jang-
dc.contributor.authorJong Seog Ahn-
dc.date.accessioned2018-01-11-
dc.date.available2018-01-11-
dc.date.issued2017-
dc.identifier.issn1932-6203-
dc.identifier.uri10.1371/journal.pone.0184339ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17447-
dc.description.abstractIn the course of searching for angiogenesis inhibitors from microorganisms, two cyclic peptides, PF1171A (1) and PF1171C (2) were isolated from the soil fungus Penicillium sp. FN070315. In the present study, we investigated the antiangiogenic efficacy and associated mechanisms of 1 and 2 in vitro using human umbilical vein endothelial cells (HUVECs). Compounds 1 and 2 inhibited the proliferation of HUVECs at concentrations not exhibiting cytotoxicity. Moreover, 1 and 2 significantly suppressed vascular endothelial growth factor (VEGF)-induced migration, invasion, proliferation and tube formation of HUVECs as well as neovascularization of the chorioallantoic membrane in developing chick embryos. We also identified an association between the antiangiogenic activity of 1 and 2 and the downregulation of both the phosphorylation of VEGF receptor 2 and the expression of hypoxia inducible factor-1α at the protein level. Taken together, these results further suggest that compounds 1 and 2 will be promising angiogenesis inhibitors.-
dc.publisherPublic Library of Science-
dc.titleTwo cyclic hexapeptides from Penicillium sp. FN070315 with antiangiogenic activities-
dc.title.alternativeTwo cyclic hexapeptides from Penicillium sp. FN070315 with antiangiogenic activities-
dc.typeArticle-
dc.citation.titlePLoS One-
dc.citation.number9-
dc.citation.endPagee0184339-
dc.citation.startPagee0184339-
dc.citation.volume12-
dc.contributor.affiliatedAuthorJun-Pil Jang-
dc.contributor.affiliatedAuthorSung-Kyun Ko-
dc.contributor.affiliatedAuthorNak Kyun Soung-
dc.contributor.affiliatedAuthorJae-Hyuk Jang-
dc.contributor.affiliatedAuthorJong Seog Ahn-
dc.contributor.alternativeName장준필-
dc.contributor.alternativeName정혜진-
dc.contributor.alternativeName한장미-
dc.contributor.alternativeName정나래-
dc.contributor.alternativeName김용효-
dc.contributor.alternativeName권호정-
dc.contributor.alternativeName고성균-
dc.contributor.alternativeName성낙균-
dc.contributor.alternativeName장재혁-
dc.contributor.alternativeName안종석-
dc.identifier.bibliographicCitationPLoS One, vol. 12, no. 9, pp. e0184339-e0184339-
dc.identifier.doi10.1371/journal.pone.0184339-
dc.description.journalClassY-
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Ochang Branch Institute > Chemical Biology Research Center > 1. Journal Articles
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