Antitumor Activity of Pyridocarbazole and Benzopyridoindole Derivatives that Inhibit Protein Kinase CK2

被引:65
作者
Prudent, Renaud [2 ]
Moucadel, Virginie [2 ]
Nguyen, Chi-Hung
Barette, Caroline [4 ]
Schmidt, Frederic [3 ]
Florent, Jean-Claude [3 ]
Lafanechere, Laurence [4 ]
Sautel, Celine F. [2 ]
Duchemin-Pelletier, Eve [2 ]
Spreux, Elodie [2 ]
Filhol, Odile [2 ]
Reiser, Jean-Baptiste [5 ]
Cochet, Claude [1 ,2 ]
机构
[1] CEA, INSERM, U873, IRTSV LTS, F-38054 Grenoble, France
[2] Univ Grenoble 1, F-38054 Grenoble, France
[3] Inst Curie, UMR 716, CNRS, Ctr Rech, F-91405 Orsay, France
[4] CEA, CNRS, UMR 5168, IRTSV CMBA, F-38054 Grenoble, France
[5] CEA CNRS UJF PSB, Inst Biol Struct Jean Pierre Ebel, F-38027 Grenoble, France
关键词
CELL-CYCLE ARREST; ELLIPTICINE; BINDING; DNA; APOPTOSIS; MUTANT; CK2-ALPHA; AGENTS; ATP;
D O I
10.1158/0008-5472.CAN-10-0917
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The alkyloid compound ellipticine derived from the berrywood tree is a topoisomerase II poison that is used in ovarian and breast cancer treatment. In this study, we report the identification of ellipticine derivatives and their tetracyclic angular benzopyridoindole analogues as novel ATP-competitive inhibitors of the protein kinase CK2. In vitro and in vivo assays showed that these compounds have a good pharmacologic profile, causing a marked inhibition of CK2 activity associated with cell cycle arrest and apoptosis in human cancer cells. Further, in vivo assays demonstrate antitumor activity in a mouse xenograft model of human glioblastoma. Finally, crystal structures of CK2-inhibitor complex provide structural insights on the molecular basis of CK2 inhibition. Our work lays the foundation for development of clinically useful CK2 inhibitors derived from a well-studied scaffold with suitable pharmacokinetics parameters. Cancer Res; 70( 23); 9865-74. (C)2010 AACR.
引用
收藏
页码:9865 / 9874
页数:10
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