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.
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John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, PolandJohn Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland
Baier, Andrea
Galicka, Anna
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Med Univ Bialystok, Dept Med Chem, Ul Mickiewicza 2a, PL-15089 Bialystok, PolandJohn Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland
Galicka, Anna
Nazaruk, Jolanta
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Med Univ Bialystok, Dept Pharmacognosy, Ul Mickiewicza 2a, PL-15089 Bialystok, PolandJohn Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland
Nazaruk, Jolanta
Szyszka, Ryszard
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John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, PolandJohn Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland