Recent Advances in the Development of Mammalian Geranylgeranyl Diphosphate Synthase Inhibitors

被引:27
|
作者
Haney, Staci L. [1 ]
Wills, Veronica S. [2 ]
Wiemer, David F. [2 ]
Holstein, Sarah A. [1 ]
机构
[1] Univ Nebraska Med Ctr, Dept Internal Med, Omaha, NE 68198 USA
[2] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
geranylgeranyl diphosphate synthase; isoprenoid; geranylgeranylation; inhibitors; NITROGEN-CONTAINING BISPHOSPHONATES; MULTIPLE-MYELOMA CELLS; ISOPRENOID BISPHOSPHONATES; TRIAZOLE BISPHOSPHONATES; PYROPHOSPHATE SYNTHASE; REDUCTASE INHIBITORS; MEVALONATE PATHWAY; PROTEIN PRENYLATION; BONE-RESORPTION; LOVASTATIN;
D O I
10.3390/molecules22060886
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The enzyme geranylgeranyl diphosphate synthase (GGDPS) catalyzes the synthesis of the 20-carbon isoprenoid geranylgeranyl diphosphate (GGPP). GGPP is the isoprenoid donor for protein geranylgeranylation reactions catalyzed by the enzymes geranylgeranyl transferase (GGTase) I and II. Inhibitors of GGDPS result in diminution of protein geranylgeranylation through depletion of cellular GGPP levels, and there has been interest in GGDPS inhibitors as potential anti-cancer agents. Here we discuss recent advances in the development of GGDPS inhibitors, including insights gained by structure-function relationships, and review the preclinical data that support the continued development of this novel class of drugs.
引用
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页数:12
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