Geranylgeranyl Diphosphate Synthase: An Emerging Therapeutic Target

被引:52
|
作者
Wiemer, A. J. [1 ,2 ]
Wiemer, D. F. [3 ,4 ]
Hohl, R. J. [1 ,2 ,4 ]
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Interdisciplinary Program Cellular & Mol Biol, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Pharmacol, Iowa City, IA 52242 USA
关键词
NITROGEN-CONTAINING BISPHOSPHONATE; ZOLEDRONIC ACID; PHASE-I; PROTEIN GERANYLGERANYLATION; ISOPRENOID BISPHOSPHONATES; INHIBITOR L-778,123; IMPROVES SURVIVAL; CYTOTOXIC AGENTS; CANCER CELLS; TUMOR-GROWTH;
D O I
10.1038/clpt.2011.215
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Proteins modified post-translationally by geranylgeranylation have been implicated in numerous cellular processes related to human disease. In recent years, the study of protein geranylgeranylation has advanced tremendously in both cellular and animal models. The advances in our understanding of the biological roles of geranylgeranylated proteins have been paralleled by advances in the medicinal chemistry of geranylgeranylation inhibitors such as those that target geranylgeranyl transferases I and II and geranylgeranyl diphosphate synthase (GGDPS). Although these findings provide the rationale for further development of geranylgeranylation as a therapeutic target, more advanced studies on the efficacy of this approach in various disease models will be required to support translation to clinical studies. This article attempts to describe the advances in (and the challenges of) validation of GGDPS as a novel therapeutic target and assesses the advantages of targeting GGDPS relative to other enzymes involved in geranylgeranylation.
引用
收藏
页码:804 / 812
页数:9
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