PLK1 as an oncology target: current status and future potential

被引:79
作者
McInnes, Campbell [1 ]
Wyatt, Michael D. [1 ]
机构
[1] Univ S Carolina, S Carolina Coll Pharm, Columbia, SC 29208 USA
关键词
POLO-LIKE KINASE; SMALL-MOLECULE INHIBITOR; DNA-DAMAGE; PHASE-I; CANCER-CELLS; BI; 2536; PROGNOSTIC-SIGNIFICANCE; MITOTIC CATASTROPHE; BREAST-CANCER; TUMOR-GROWTH;
D O I
10.1016/j.drudis.2011.05.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The Polo-like kinases (PLKs) have been investigated as oncology targets for several years; however, only recently have potent inhibitors been described. Here, we report on progress in the clinical validation of the PLKs as antitumor drug targets as well as recent understanding gained regarding their synergistic roles in the context of other molecular defects occurring in tumors. Also relevant to the development of PLK inhibitors as therapeutics are the putative roles of other members of this family as tumor. suppressors. The resulting potential drawbacks of non-isoform selective compounds are presented. As an alternative approach to achieving PLK1 specificity, we discuss prospects for developing small molecule inhibitors of the crucial regulatory and subcellular targeting domain containing the Polo-boxes.
引用
收藏
页码:619 / 625
页数:7
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