共 26 条
Mycoepoxydiene, a fungal polyketide, induces cell cycle arrest at the G2/M phase and apoptosis in HeLa cells
被引:40
作者:
Wang, Jifeng
[1
]
Zhao, Baobing
[1
]
Zhang, Wei
[1
]
Wu, Xuan
[1
]
Wang, Ruoyu
[1
]
Huang, Yaojian
[1
]
Chen, Dong
[2
,3
,4
]
Park, Kum
[4
]
Weimer, Bart C.
[2
,3
,4
]
Shen, Yuemao
[1
,2
,3
]
机构:
[1] Xiamen Univ, Sch Life Sci, Minist Educ Cell Biol & Tumor Cell Engn, Key Lab, Xiamen 361005, Fujian, Peoples R China
[2] Xiamen Univ, Joint Ctr Syst Biol, Xiamen 361005, Fujian, Peoples R China
[3] Xiamen Univ, Utah State Univ, Xiamen 361005, Fujian, Peoples R China
[4] Utah State Univ, Ctr Integrated BioSyst, Logan, UT 84322 USA
基金:
美国农业部;
关键词:
Mycoepoxydiene;
Polyketide;
G2/M arrest;
MAPK;
Apoptosis;
NATURAL-PRODUCTS;
CANCER;
KINASE;
METABOLITES;
PATHWAYS;
SKELETON;
STRESS;
DRUGS;
D O I:
10.1016/j.bmcl.2010.09.105
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Mycoepoxydiene (MED) is a polyketide isolated from a marine fungus associated with mangrove forests. It contains an oxygen-bridged cyclooctadiene core and an alpha,beta-unsaturated delta-lactone moiety. MED induced the reorganization of cytoskeleton in actively growing HeLa cells by promoting formation of actin stress fiber and inhibiting polymerization of tubulin. MED could induce cell cycle arrest at G2/M in HeLa cells. MED-associated apoptosis was characterized by the formation of fragmented nuclei, PARP cleavage, cytochrome c release, activation of caspase-3, and an increased proportion of sub-G1 cells. Additionally, MED activated MAPK pathways. Interestingly, the time of JNK, p38, and Bcl-2 activation did not correlate with the release of cytochrome c. This study is the first report demonstrating the action mechanism of MED against tumor cell growth. These results provide the potential of MED as a novel low toxic antitumor agent. (C) 2010 Elsevier Ltd. All rights reserved.
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页码:7054 / 7058
页数:5
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