GSK-3 inhibitors: preclinical and clinical focus on CNS

被引:286
作者
Eldar-Finkelman, Hagit [1 ]
Martinez, Ana [2 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, Dept Human Mol Genet & Biochem, IL-69978 Tel Aviv, Israel
[2] CSIC, Inst Quim Med, E-28006 Madrid, Spain
关键词
protein kinases; GSK-3; inhibitors; CNS; GLYCOGEN-SYNTHASE KINASE-3; NEURONAL CELL-DEATH; BETA-CATENIN STABILIZATION; SMALL-MOLECULE INHIBITORS; CYCLIN-DEPENDENT KINASES; INSULIN-MIMETIC ACTION; WNT SIGNALING PATHWAY; EMBRYONIC STEM-CELLS; PROTEIN-KINASE; ALZHEIMERS-DISEASE;
D O I
10.3389/fnmol.2011.00032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Inhibiting glycogen synthase kinase-3 (GSK-3) activity via pharmacological intervention has become an important strategy for treating neurodegenerative and psychiatric disorders. The known GSK-3 inhibitors are of diverse chemotypes and mechanisms of action and include compounds isolated from natural sources, cations, synthetic small-molecule ATP-competitive inhibitors, non-ATP-competitive inhibitors, and substrate competitive inhibitors. Here we describe the variety of GSK-3 inhibitors with a specific emphasis on their biological activities in neurons and neurological disorders. We further highlight our current progress in the development of non-ATP-competitive inhibitors of GSK-3. The available data raise the hope that one or more of these drug design approaches will prove successful at stabilizing or even reversing the aberrant neuropathology and cognitive deficits of certain central nervous system disorders.
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页数:18
相关论文
共 223 条
[21]   Induction of the wnt inhibitor, dickkopf-1, is associated with neurodegeneration related to temporal lobe epilepsy [J].
Busceti, Carla Letizia ;
Biagioni, Francesca ;
Aronica, Eleonora ;
Riozzi, Barbara ;
Storto, Marianna ;
Battaglia, Giuseppe ;
Giorgi, Filippo S. ;
Gradini, Roberto ;
Fornai, Francesco ;
Caricasole, Andrea ;
Nicoletti, Ferdinando ;
Bruno, Valeria .
EPILEPSIA, 2007, 48 (04) :694-705
[22]   Lithium reduces tau phosphorylation but not Aβ or working memory deficits in a transgenic model with both plaques and tangles [J].
Caccamo, Antonella ;
Oddo, Salvatore ;
Tran, Lana X. ;
LaFerla, Frank M. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 170 (05) :1669-1675
[23]   Glycogen synthase kinase-3β inhibitors prevent cellular polyglutamine toxicity caused by the Huntington's disease mutation [J].
Carmichael, J ;
Sugars, KL ;
Bao, YP ;
Rubinsztein, DC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (37) :33791-33798
[24]   Nuclear GSK-3β inhibits the canonical Wnt signalling pathway in a β-catenin phosphorylation-independent manner [J].
Caspi, M. ;
Zilberberg, A. ;
Eldar-Finkelman, H. ;
Rosin-Arbesfeld, R. .
ONCOGENE, 2008, 27 (25) :3546-3555
[25]   GSK-3β inhibition/β-catenin stabilization in ventral midbrain precursors increases differentiation into dopamine neurons [J].
Castelo-Branco, G ;
Rawal, N ;
Arenas, E .
JOURNAL OF CELL SCIENCE, 2004, 117 (24) :5731-5737
[26]   Glycogen synthase kinase 3β (GSK3β) mediates 6-hydroxydopamine-induced neuronal death [J].
Chen, G ;
Bower, KA ;
Ma, CL ;
Fang, SY ;
Thiele, CJ ;
Luo, J .
FASEB JOURNAL, 2004, 18 (07) :1162-+
[27]  
CHENG K, 1983, MOL CELL BIOCHEM, V56, P183
[28]   Synthesis and biological evaluation of 3,6-diamino-1H-pyrazolo[3,4-b]pyridine derivatives as protein kinase inhibitors [J].
Chioua, Mourad ;
Samadi, Abdelouahid ;
Soriano, Elena ;
Lozach, Olivier ;
Meijer, Laurent ;
Marco-Contelles, Jose .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2009, 19 (16) :4566-4569
[29]   In search of the holy grail for the treatment of neurodegenerative disorders: Has a simple cation been overlooked? [J].
Chuang, De-Maw ;
Manji, Husseini K. .
BIOLOGICAL PSYCHIATRY, 2007, 62 (01) :4-6
[30]   ISOLATION AND X-RAY CRYSTAL-STRUCTURE OF A NOVEL BROMO-COMPOUND FROM 2 MARINE SPONGES [J].
CIMINO, G ;
DEROSA, S ;
DESTEFANO, S ;
MAZZARELLA, L ;
PULITI, R ;
SODANO, G .
TETRAHEDRON LETTERS, 1982, 23 (07) :767-768