Challenges and opportunities with glycogen synthase kinase-3 inhibitors for insulin resistance and Type 2 diabetes treatment

被引:40
作者
Eldar-Finkelman, H [1 ]
Ilouz, R [1 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, Dept Human Genet & Mol Med, Ramat Aviv, Israel
关键词
GSK-3; insulin resistance; protein kinase inhibitors; Type; 2; diabetes;
D O I
10.1517/13543784.12.9.1511
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The role of the serine/threonine protein kinase, glycogen synthase kinase-3 (GSK-3), in attenuating the insulin signalling pathway has led to the concept that inhibition of GSK-3 may have therapeutic benefits in the treatment of insulin resistance and Type 2 diabetes. Indeed, various selective GSK-3 inhibitors have been developed recently and have proven to promote insulin-like effects and to act as insulin sensitisers in both in vitro and in vivo systems. GSK-3 inhibition may thus present a new, effective approach for the treatment of insulin resistance and Type 2 diabetes. This review describes the qualifications of GSK-3 as a novel drug-discovery target for Type 2 diabetes and discusses the strategies and challenges in developing small-molecule inhibitors for this important protein kinase.
引用
收藏
页码:1511 / 1519
页数:9
相关论文
共 82 条
[61]   Conformational diversity of catalytic cores of protein kinases [J].
Sowadski, JM ;
Epstein, LF ;
Lankiewicz, L ;
Karlsson, R .
PHARMACOLOGY & THERAPEUTICS, 1999, 82 (2-3) :157-164
[62]   Lithium inhibits glycogen synthase kinase-3 activity and mimics Wingless signalling in intact cells [J].
Stambolic, V ;
Ruel, L ;
Woodgett, JR .
CURRENT BIOLOGY, 1996, 6 (12) :1664-1668
[63]  
TANTI JF, 1994, J BIOL CHEM, V269, P6051
[64]   A TEMPLATE FOR THE PROTEIN-KINASE FAMILY [J].
TAYLOR, SS ;
KNIGHTON, DR ;
ZHENG, JH ;
SOWADSKI, JM ;
GIBBS, CS ;
ZOLLER, MJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (03) :84-89
[65]   Protein kinase inhibition: natural and synthetic variations on a theme [J].
Taylor, SS ;
Radzio-Andzelm, E .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1997, 1 (02) :219-226
[66]   Structure of GSK3β reveals a primed phosphorylation mechanism [J].
ter Haar, E ;
Coll, JT ;
Austen, DA ;
Hsiao, HM ;
Swenson, L ;
Jain, J .
NATURE STRUCTURAL BIOLOGY, 2001, 8 (07) :593-596
[67]   A GSK3-binding peptide from FRAT1 selectively inhibits the GSK3-catalysed phosphorylation of Axin and β-catenin [J].
Thomas, GM ;
Frame, S ;
Goedert, M ;
Nathke, I ;
Polakis, P ;
Cohen, P .
FEBS LETTERS, 1999, 458 (02) :247-251
[68]  
Toledo LM, 1999, CURR MED CHEM, V6, P775
[69]   Strategies toward the design of novel and selective protein tyrosine kinase inhibitors [J].
Traxler, P ;
Furet, P .
PHARMACOLOGY & THERAPEUTICS, 1999, 82 (2-3) :195-206
[70]   Protein-protein interaction in insulin signaling and the molecular mechanisms of insulin resistance [J].
Virkamäki, A ;
Ueki, K ;
Kahn, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (07) :931-943