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
[1]   Validating cancer drug targets [J].
Benson, John D. ;
Chen, Ying-Nan P. ;
Cornell-Kennon, Susan A. ;
Dorsch, Marion ;
Kim, Sunkyu ;
Leszczyniecka, Magdalena ;
Sellers, William R. ;
Lengauer, Christoph .
NATURE, 2006, 441 (7092) :451-456
[2]  
Butler MS, 2005, NAT PROD REP, V22, P162, DOI 10.1039/b402985m
[3]   Mycoepoxydiene represents a novel class of fungal metabolites [J].
Cai, P ;
McPhail, AT ;
Krainer, E ;
Katz, B ;
Pearce, C ;
Boros, C ;
Caceres, B ;
Smith, D ;
Houck, DR .
TETRAHEDRON LETTERS, 1999, 40 (08) :1479-1482
[4]   Timeline - Chemotherapy and the war on cancer [J].
Chabner, BA ;
Roberts, TG .
NATURE REVIEWS CANCER, 2005, 5 (01) :65-72
[5]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[6]   Oligomeric Bax is a component of the putative cytochrome c release channel MAC, mitochondrial apoptosis-induced channel [J].
Dejean, LM ;
Martinez-Caballero, S ;
Guo, L ;
Hughes, C ;
Teijido, O ;
Ducret, T ;
Ichas, F ;
Korsmeyer, SJ ;
Antonsson, B ;
Jonas, EA ;
Kinnally, KW .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (05) :2424-2432
[7]   Trichostatin A causes p53 to switch oxidative-damaged colorectal cancer cells from cell cycle arrest into apoptosis [J].
Habold, C. ;
Poehlmann, A. ;
Bajbouj, K. ;
Hartig, R. ;
Korkmaz, K. S. ;
Roessner, A. ;
Schneider-Stock, R. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2008, 12 (02) :607-621
[8]   Geldanamycin interferes with the 90-kDa heat shock protein, affecting lipopolysaccharide-mediated interleukin-1 expression and apoptosis within macrophages [J].
Hsu, Hsien-Yeh ;
Wu, Hua-Lin ;
Tan, Sai-Koong ;
Li, Vivian Pei-Hsin ;
Wang, Wei-Ting ;
Hsu, Jason ;
Cheng, Ching-Hsun .
MOLECULAR PHARMACOLOGY, 2007, 71 (01) :344-356
[9]   Mitochondrial control of apoptosis [J].
Kroemer, G ;
Zamzami, N ;
Susin, SA .
IMMUNOLOGY TODAY, 1997, 18 (01) :44-51
[10]   Signal transduction through MAP kinase cascades [J].
Lewis, TS ;
Shapiro, PS ;
Ahn, NG .
ADVANCES IN CANCER RESEARCH, VOL 74, 1998, 74 :49-139