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一种酚类化合物,5-咖啡酰奎宁酸(绿原酸),是一种新型且强效的基质金属蛋白酶-9抑制剂:从翅卫矛甲醇提取物中分离与鉴定。

A phenolic compound, 5-caffeoylquinic acid (chlorogenic acid), is a new type and strong matrix metalloproteinase-9 inhibitor: isolation and identification from methanol extract of Euonymus alatus.

作者信息

Jin Un-Ho, Lee Ji-Young, Kang Sung-Koo, Kim June-Ki, Park Won-Hwan, Kim Jong-Guk, Moon Sung-Kwon, Kim Cheorl-Ho

机构信息

Department of Biochemistry and Molecular Biology, Dongguk University College of Oriental Medicine and National Research Laboratory for Glycobiology, Kyungju, Kyungbuk 780-714, Republic of Korea.

出版信息

Life Sci. 2005 Oct 14;77(22):2760-9. doi: 10.1016/j.lfs.2005.02.028.

DOI:10.1016/j.lfs.2005.02.028
PMID:16005473
Abstract

A phenolic compound responsible for anti-MMP-9, which is known to be involved in tumor cell invasion and metastasis, has been isolated from methanol extracts prepared from stem barks of Euonymus alatus by assay-guided fractionation. The compound has been identified as 5-caffeoylquinic acid (chlorogenic acid; CHA) by NMR and FAB-MS. CHA showed a strong inhibitory effect of matrix metalloproteinase (MMP)-9 activity in a concentration-dependent manner on zymography. The purified CHA inhibited MMP-9 activity with the IC50 of 30-50 nM. Furthermore, the cytotoxic survival curve showed that CHA does not have cytotoxic effects on cellular proliferation, when Hep3B cells were treated with various concentrations of CHA and cell viability was measured using the XTT assay. The present data suggest a clue for possible mechanisms of cancer chemoprevention by CHA and other naturally occurring phenolic compounds. The results also imply that useful cancer chemopreventive agents can be further identified by combinations of in vitro (as a first screen) and in vivo studies.

摘要

通过活性导向分离法,从卫矛茎皮的甲醇提取物中分离出一种具有抗基质金属蛋白酶-9(MMP-9)作用的酚类化合物,已知MMP-9参与肿瘤细胞的侵袭和转移。通过核磁共振(NMR)和快原子轰击质谱(FAB-MS),该化合物被鉴定为5-咖啡酰奎宁酸(绿原酸;CHA)。在酶谱分析中,CHA对基质金属蛋白酶(MMP)-9活性表现出浓度依赖性的强烈抑制作用。纯化后的CHA抑制MMP-9活性的半数抑制浓度(IC50)为30-50 nM。此外,细胞毒性存活曲线表明,当用不同浓度的CHA处理Hep3B细胞并使用XTT法测定细胞活力时,CHA对细胞增殖没有细胞毒性作用。目前的数据为CHA和其他天然存在的酚类化合物可能的癌症化学预防机制提供了线索。结果还表明,通过体外(作为初步筛选)和体内研究相结合,可以进一步鉴定出有用的癌症化学预防剂。

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