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.
引用
收藏
页码:7054 / 7058
页数:5
相关论文
共 26 条
[21]   Natural Products and Colon Cancer: Current Status and Future Prospects [J].
Rajamanickam, Subapriya ;
Agarwal, Rajesh .
DRUG DEVELOPMENT RESEARCH, 2008, 69 (07) :460-471
[22]   Double identity for proteins of the Bcl-2 family [J].
Reed, JC .
NATURE, 1997, 387 (6635) :773-776
[23]   Asymmetric total syntheses of (+)-mycoepoxydiene and related natural product (-)-1893A: Application of one-pot ring-opening/cross/ring-closing metathesis to construct their 9-oxabicyclo[4.2.1]nona-2,4-diene skeleton [J].
Takao, K ;
Yasui, H ;
Yamamoto, S ;
Sasaki, D ;
Kawasaki, S ;
Watanabe, G ;
Tadano, K .
JOURNAL OF ORGANIC CHEMISTRY, 2004, 69 (25) :8789-8795
[24]   Total synthesis of (±)-mycoepoxydiene, a novel fungal metabolite having an oxygen-bridged cyclooctadiene skeleton [J].
Takao, K ;
Watanabe, G ;
Yasui, H ;
Tadano, K .
ORGANIC LETTERS, 2002, 4 (17) :2941-2943
[25]   Ribotoxic mycotoxin deoxynivalenol induces G2/M cell cycle arrest via P21Cip/WAF1 mRNA stabilization in human epithelial cells [J].
Yang, Hyun ;
Chung, Duk Hwa ;
Kim, Yung Bu ;
Choi, Yung Hyun ;
Moon, Yuseok .
TOXICOLOGY, 2008, 243 (1-2) :145-154
[26]   An APAF-1•cytochrome c multimeric complex is a functional apoptosome that activates procaspase-9 [J].
Zou, H ;
Li, YC ;
Liu, HS ;
Wang, XD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :11549-11556