Anti-mitotic properties of indirubin-3'-monoxime, a CDK/GSK-3 inhibitor: induction of endoreplication following prophase arrest

被引:135
作者
Damiens, E
Baratte, B
Marie, D
Eisenbrand, G
Meijer, L
机构
[1] CNRS, Biol Stn, Cell Cycle Grp, F-29682 Roscoff, France
[2] Univ Kaiserslautern, Div Food Chem & Environm Toxicol, Dept Chem, D-67663 Kaiserslautern, Germany
[3] CNRS, Phytoplankton Ocean Grp, Biol Stn, F-29682 Roscoff, France
关键词
cyclin-dependent kinase; glycogen synthase kinase; GSK-3; beta; indirubin; kinase inhibitor; cancer;
D O I
10.1038/sj.onc.1204503
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bis-indole indirubin is the active ingredient of the Traditional Chinese Medicine recipe Danggui Longhui Wan used against chronic myelocytic leukemia, We have previously shown that indirubins are potent inhibitors of cyclin-dependent kinases and glycogen synthase kinase-3, We here investigated the anti-mitotic properties of this class of compounds using the cell permeable indirubin-3 ' -monoxime and the HBL-100 cell line. Indirubin-3 ' -monoxime reversibly arrests asynchronous HBL-100 cells in G2, This arrest is not accompanied by any significant change in expression of the major cell cycle regulators, However indirubin-3 ' -monoxime inhibits the phosphorylation of consensus CDK phosphorylation sites as well as of nucleolin at a specific CDK1/cyclin B phosphorylation site, suggesting a direct action on the mitotic CDK1/cyclin B, When indirubin-3 ' -monoxime is added to HBL-100 cells synchronized in M phase by nocodazole, cells undergo an endoreplication leading to an 8n DNA content. As soon as indirubin-3 ' -monoxime is washed away, these polyploid cells become aneuploid and later die from necrosis, This mechanism of endoreplication followed by cell death may contribute to the antitumour properties of indirubins.
引用
收藏
页码:3786 / 3797
页数:12
相关论文
共 36 条
  • [1] Differential effects of UCN-01, staurosporine and CGP 41 251 on cell cycle progression and CDC2 cyclin B1 regulation in A431 cells synchronized at M phase by nocodazole
    Akiyama, T
    Shimizu, M
    Okabe, W
    Tamaoki, T
    Akinaga, S
    [J]. ANTI-CANCER DRUGS, 1999, 10 (01) : 67 - 78
  • [2] Atienza C, 2000, INT J MOL MED, V6, P55
  • [3] Cell cycle arrest and DNA endoreduplication following p21Waf1/Cip1 expression
    Bates, S
    Ryan, KM
    Phillips, AC
    Vousden, KH
    [J]. ONCOGENE, 1998, 17 (13) : 1691 - 1703
  • [4] Bible KC, 1997, CANCER RES, V57, P3375
  • [5] The search for and potential therapeutic applications of chemical inhibitors of cyclin-dependent kinases
    Borgne, A
    Meijer, L
    [J]. M S-MEDECINE SCIENCES, 1999, 15 (04): : 496 - 503
  • [6] Sequential dephosphorylation of p34(cdc2) on Thr-14 and Tyr-15 at the prophase/metaphase transition
    Borgne, A
    Meijer, L
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (44) : 27847 - 27854
  • [7] Brodsky W Y, 1977, Int Rev Cytol, V50, P275
  • [8] Chang CN, 1985, ADV CHINESE MED MAT, P369
  • [9] CHEN DH, 1984, CHINESE TRAD HERBAL, V15, P6
  • [10] Cdk inhibitors, roscovitine and olomoucine, synergize with farnesyltransferase inhibitor (FTI) to induce efficient apoptosis of human cancer cell lines
    Edamatsu, H
    Gau, CL
    Nemoto, T
    Guo, L
    Tamanoi, F
    [J]. ONCOGENE, 2000, 19 (27) : 3059 - 3068