Phlorofucofuroeckol-A, a Potent Inhibitor of Aldo-keto Reductase Family 1 Member B10, from the Edible Brown Alga Eisenia bicyclis

Authors
Lee, Joo YoungKim, Sang MinJung, Woo-SukSong, Dae-GeunUm, Byung-HunSon, Jin-KiPan, Cheol-Ho
Issue Date
2012-12
Publisher
KOREAN SOC APPLIED BIOLOGICAL CHEMISTRY
Citation
JOURNAL OF THE KOREAN SOCIETY FOR APPLIED BIOLOGICAL CHEMISTRY, v.55, no.6, pp.721 - 727
Abstract
Aldo-keto reductase family 1 member B10 (AKR1B10) belongs to a superfamily of NADPH-dependent aldo-keto reductases and is considered a biomarker of several cancers. Inhibition of recombinant human AKR1B10 (rhAKR1B10) was assayed using 31 seaweed extracts, among which, an Eisenia bicyclis extract was selected for further study. To identify the compounds in E. bicyclis responsible for inhibitory effects on rhAKR1B10, five compounds were isolated by bioactivity-guided fractionation and isolation. Among them, phlorofucofuroeckol-A (PFF-A), isolated from an ethyl acetate fraction, exhibited the greatest inhibition of rhAKR1B10. The inhibitory rate of PFF-A against rhAKR1B10 was 61.41% at 10 mu M, with an IC50 of 6.22 mu M. Enzyme kinetic analyses revealed non-competitive inhibition with a K-D of 2.76 mu M. These results indicate that PFF-A from E. bicyclis may be a promising anticancer agent.
Keywords
ECKLONIA-KUROME; PHLOROTANNINS; AKR1B10; IDENTIFICATION; PURIFICATION; METABOLISM; MARKER; TARGET; 1B10; ECKLONIA-KUROME; PHLOROTANNINS; AKR1B10; IDENTIFICATION; PURIFICATION; METABOLISM; MARKER; TARGET; 1B10; aldo-keto reductase; aldo-keto reductase family 1 member B10; Eisenia bicyclis; phlorofucofuroeckol-A; phlorotannins
ISSN
1738-2203
URI
https://pubs.kist.re.kr/handle/201004/128616
DOI
10.1007/s13765-012-2169-3
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KIST Article > 2012
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