The 14-3-3ζ-GPM-IX-V complex as an antiplatelet target

被引:21
作者
Andrews, Robert K.
Du, Xiaoping
Berndt, Michael C.
机构
[1] Monash Univ, Dept Immunol, Alfred Med Res & Educ Precinct, Melbourne, Vic 3004, Australia
[2] Univ Illinois, Coll Med, Dept Pharmacol, Chicago, IL USA
关键词
D O I
10.1358/dnp.2007.20.5.1120215
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The functional nexus involving the platelet adhesion receptor, the glycoprotein (GP)Ib-IX-V complex, and the signaling protein, 14-3-3 zeta, is emerging as a new drug target for control of GPIb-IX-V-dependent thrombotic diseases such as heart attack and stroke. Together, advances in understanding mechanisms of regulation and functional consequences of the GPIb-IX-V/14-3-3 zeta interaction, and the growing potential of 14-3-3-targeting therapeutic approaches used for 14-3-3-dependent processes in other cells-principally involving cell cycling and cancer-point to 14-3-3 zeta as a promising antithrombotic target. The unique recognition sequences and arrangement of functional 14-3-3 zeta-binding sites found within the cytoplasmic domain of GPlb-IX-V increase the likelihood of selective targeting of this interaction. (c) 2007 Prous Science. All rights reserved.
引用
收藏
页码:285 / 292
页数:8
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