Haspin: a promising target for the design of inhibitors as potent anticancer drugs

被引:45
作者
Amoussou, Nathalie Gisele [1 ,2 ]
Bigot, Andre [3 ]
Roussakis, Christos [1 ]
Robert, Jean-Michel H. [1 ]
机构
[1] Univ Nantes, Nantes Atlantique Univ, Cibles & Medicaments Canc & Immunite IICiMed AE11, Inst Rech Sante 2, 22 Rue Benoni Goulin, F-44000 Nantes, France
[2] Univ Abomey Calavi, Fac Sci Sante, Lab Chim Pharmaceut Organ, 01 BP 188, Cotonou, Benin
[3] Univ Abomey Calavi, Fac Sci Sante, Unite Enseignement & Rech Immunol, 01 BP 188, Cotonou, Benin
关键词
PROTEIN-KINASE INHIBITORS; AURORA-B; HISTONE H3; THR-3; PHOSPHORYLATION; CATALYTIC DOMAIN; MITOSIS; CENTROMERES; HARMINE; DYRK1A; CELLS;
D O I
10.1016/j.drudis.2017.10.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Protein kinases constitute a large group of enzymes in eukaryotes and have an important role in many cellular processes. Several of these proteins are active kinases, such as haploid germ cell-specific nuclear protein kinase (Haspin), an atypical eukaryotic protein kinase that lacks sequence similarity with other eukaryotic protein kinases. Haspin is a serine/threonine kinase that associates with chromosome and phosphorylates threonine 3 of histone 3 during mitosis. Haspin overexpression or deletion results in defective mitosis. It has been shown that Haspin inhibitors have potent anti-tumoral effects. Given that the only Haspin substrate is threonine 3 of histone 3, inhibition of Haspin might have fewer adverse effects compared with other anticancer agents. Here, we highlight the chemical structures and actions of currently known Haspin inhibitors.
引用
收藏
页码:409 / 415
页数:7
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