Inhibitory effects of polyphenols isolated from Rhus verniciflua on Aldo-keto reductase family 1 B10

Authors
Song, Dae-GeunLee, Joo YoungLee, Eun HaJung, Sang HoonNho, Chu WonCha, Kwang HyunKoo, Song YiPan, Cheol-Ho
Issue Date
2010-04-30
Publisher
KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
Citation
BMB REPORTS, v.43, no.4, pp.268 - 272
Abstract
Aldo-keto reductase family 1 B10 (AKR1B10) is a member of the NADPH-dependent aldo-keto reductase (AKR) superfamily, and has been considered to be a potential cancer therapeutic target. Total extract from the bark of Rhus verniciflua (Toxicodendron vernicifluum (Stokes)) showed AKR1B10 inhibitory activity. To identify the active compounds from R. verniciflua responsible for AKR1B10 inhibition, nine compounds were isolated via bioactivity-guided isolation and tested for their effects against recombinant human AKR1B10 (rhAKR1B10). Results showed that butein, isolated from the ethyl acetate fraction, was most able to inhibit rhAKR1B10. The inhibitory rate of butein against rhAKR1B10 was 42.86% at 1 mu M with an IC50 value of 1.47 mu M, and enzyme kinetic analysis revealed its inhibition mode to be uncompetitive. [BMB reports 2010; 43(4): 268-272]
Keywords
TUMOR-MARKER AKR1B10; NF-KAPPA-B; CANCER CELLS; CARCINOMAS; SORBINIL; SMOKERS; MEMBER; GENE; TUMOR-MARKER AKR1B10; NF-KAPPA-B; CANCER CELLS; CARCINOMAS; SORBINIL; SMOKERS; MEMBER; GENE; AKR1B10; Aldo-keto reductase; Aldose reductase-like; Anticancer; Butein; Polyphenol; Rhus verniciflua
ISSN
1976-6696
URI
https://pubs.kist.re.kr/handle/201004/131533
DOI
10.5483/BMBRep.2010.43.4.268
Appears in Collections:
KIST Article > 2010
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