包永明

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:生物工程学院

学科:生物化工. 生物化学与分子生物学. 生物工程与技术

办公地点:大连理工大学生物工程楼323;盘锦校区D06 302室

联系方式:E-mail:biosci@dlut.edu.cn Tel:13332280036

电子邮箱:biosci@dlut.edu.cn

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Directional modification of chrysin for exerting apoptosis and enhancing significantly anti-cancer effects of 10-hydroxy camptothecin

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论文类型:期刊论文

发表时间:2016-08-01

发表刊物:BIOMEDICINE & PHARMACOTHERAPY

收录刊物:SCIE、PubMed、Scopus

卷号:82

页面范围:693-703

ISSN号:0753-3322

关键字:Chrysin, 5-(2 '-amino) phenyl-7-cyclohexanemethylchrysin (Ch-1); 10-Hydroxy camptothecin; DNA intercalator; Apoptosis; Synergy

摘要:Chrysin, one of natural flavonoid compounds, has recently been found to possess anti-inflammatory, antiallergic and anticancer properties. To increase its anticancer effects, 5 chrysin derivates were synthesized on the base of DNA intercalator structure. The inhibiting effects of chrysin and its derivatives on cancer cells Hela, BGC823, MCF-7, HepG2, and normal cells HEK-293, were evaluated by MTT assays. 5-(2'-amino) phenyl-7-cyclohexanemethylchrysin (Ch-1), a unique chrysin derivate, killed all the cancer cells but kept above 60% survival rate in normal cells HEK-293 at 62.5 mu M. Treated with chrysin from 250 mM to 500 mM, those cells were still maintained above 60% survival rate. The result of circular dichroism spectra showed that Ch-1 could intercalate DNA while chrysin had no effects on DNA. Interestingly, Hela cells survival rates were 95% and 10%, after treated with 20 mM and 30 mM of Ch-1, respectively. Both intrinsic and extrinsic apoptotic pathway were identified in regulating the cell death caused by Ch-1 in Hela cells. p53, the upstream regulator of apoptotic pathway were extremely significantly up-regulated in Hela cells treated with 25 mM Ch-1. Moreover, the inhibiting effects and apoptotic related proteins responses to Ch-1 on Hela cells were abolished after pre-treated with Pifithrin-alpha (Pft-alpha), a p53 inhibitor. So, p53-depedent apoptosis is the crucial factor governing the inhibiting effects of Ch-1 in Hela cells. Amazingly, Ch-1 at non-toxic concentration (2.5-10 mu M) enhanced significantly anti-cancer effect of 10-hydroxy camptothecin (HCPT) on Hela, BGC823, and MCF-7 cells. (C) 2016 Elsevier Masson SAS. All rights reserved.