Functional Characterization of CFI-400945, a Polo-like Kinase 4 Inhibitor, as a Potential Anticancer Agent

被引:148
作者
Mason, Jacqueline M. [2 ]
Lin, Dan Chi-Chia [2 ]
Wei, Xin [2 ]
Che, Yi [2 ]
Yao, Yi [2 ]
Kiarash, Reza [2 ]
Cescon, David W. [1 ]
Fletcher, Graham C. [2 ]
Awrey, Donald E. [2 ]
Bray, Mark R. [2 ]
Pan, Guohua [2 ]
Mak, Tak W. [1 ]
机构
[1] Campbell Family Inst Breast Canc Res, Toronto, ON M5G 2M9, Canada
[2] Campbell Family Inst Breast Canc Res, Toronto, ON M5G 1L7, Canada
基金
加拿大健康研究院;
关键词
EXPRESSION SIGNATURE; DNA-REPAIR; BREAST; AURORA; PLK4; GENE; P53; OVERDUPLICATION; AMPLIFICATION; DUPLICATION;
D O I
10.1016/j.ccr.2014.05.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PLK4 was identified as a promising therapeutic target through a systematic approach that combined RNAi screening with gene expression analysis in human breast cancers and cell lines. A drug discovery program culminated in CFI-400945, a potent and selective PLK4 inhibitor. Cancer cells treated with CFI-400945 exhibit effects consistent with PLK4 kinase inhibition, including dysregulated centriole duplication, mitotic defects, and cell death. Oral administration of CFI-400945 to mice bearing human cancer xenografts results in the significant inhibition of tumor growth at doses that are well tolerated. Increased antitumor activity in vivo was observed in PTEN-deficient compared to PTEN wild-type cancer xenografts. Our findings provide a rationale for the clinical evaluation of CFI-400945 in patients with solid tumors, in particular those deficient in PTEN.
引用
收藏
页码:163 / 176
页数:14
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