Antileukemia component, dehydroeburicoic acid from Antrodia camphorata induces DNA damage and apoptosis in vitro and in vivo models

被引:44
作者
Du, Ying-Chi [2 ]
Chang, Fang-Rong [2 ,3 ,4 ,5 ]
Wu, Tung-Ying [2 ]
Hsu, Yu-Ming [2 ]
El-Shazly, Mohamed [2 ,6 ]
Chen, Chieh-Fu [7 ]
Sung, Ping-Jyun [1 ,8 ]
Lin, Yan-Yu [2 ]
Lin, Yi-Hsin [2 ]
Wu, Yang-Chang [2 ,9 ,10 ,11 ]
Lu, Mei-Chin [1 ,2 ,7 ,8 ]
机构
[1] Natl Dong Hwa Univ, Grad Inst Marine Biotechnol, Pingtung 944, Taiwan
[2] Kaohsiung Med Univ, Coll Pharm, Grad Inst Nat Prod, Kaohsiung 807, Taiwan
[3] Kaohsiung Med Univ Hosp, Ctr Canc, Kaohsiung 807, Taiwan
[4] Kaohsiung Med Univ, Coll Pharm, Res & Dev Ctr Chinese Herbal Med & New Drugs, Kaohsiung 807, Taiwan
[5] Natl Sun Yat Sen Univ, Dept Marine Biotechnol & Resources, Kaohsiung 804, Taiwan
[6] Ain Shams Univ, Fac Pharm, Dept Pharmacognosy & Nat Prod Chem, Cairo, Egypt
[7] Chih Ying Plant Res & Dev Fdn, Taipei 100, Taiwan
[8] Natl Museum Marine Biol & Aquarium, Pingtung 944, Taiwan
[9] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung 404, Taiwan
[10] China Med Univ Hosp, Nat Med Prod Res Ctr, Taichung 404, Taiwan
[11] China Med Univ Hosp, Ctr Mol Med, Taichung 404, Taiwan
关键词
Antrodia camphorata; Dehydroeburicoic acid (DeEA); DNA damage; Apoptosis; Topoisomerase II inhibitor; CELLS; CYTOTOXICITY; GAMMA-H2AX; INHIBITORS;
D O I
10.1016/j.phymed.2012.03.014
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Antrodia camphorata (AC) is a native Taiwanese mushroom which is used in Asian folk medicine as a chemopreventive agent. The triterpenoid-rich fraction (FEA) was obtained from the ethanolic extract of AC and characterized by high performance liquid chromatography (HPLC). FEA caused DNA damage in leukemia HL 60 cells which was characterized by phosphorylation of H2A.X and Chk2. It also exhibited apoptotic effect which was correlated to the enhancement of PARP cleavage and to the activation of caspase 3. Five major triterpenoids, antcin K (1), antcin C (2), zhankuic acid C (3), zhankuic acid A (4), and dehydroeburicoic acid (5) were isolated from FEA. The cytotoxicity of FEA major components (1-5) was investigated showing that dehydroeburicoic acid (DeEA) was the most potent cytotoxic component. DeEA activated DNA damage and apoptosis biomarkers similar to FEA and also inhibited topoisomerase II. In HL 60 cells xenograft animal model, DeEA treatment resulted in a marked decrease of tumor weight and size without any significant decrease in mice body weights. Taken together, our results provided the first evidence that pure AC component inhibited tumor growth in vivo model backing the traditional anticancer use of AC in Asian countries. (C) 2012 Elsevier GmbH. All rights reserved.
引用
收藏
页码:788 / 796
页数:9
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