Cell cycle proteins as promising targets in cancer therapy

被引:1284
|
作者
Otto, Tobias [1 ,2 ,3 ]
Sicinski, Piotr [1 ,2 ]
机构
[1] Harvard Med Sch, Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02215 USA
[2] Harvard Med Sch, Dept Genet, Boston, MA 02215 USA
[3] Univ Hosp RWTH Aachen, Dept Internal Med 3, D-52074 Aachen, Germany
关键词
DEPENDENT KINASE INHIBITOR; POLO-LIKE-KINASE; VOLASERTIB BI 6727; PHASE-II TRIAL; INVESTIGATIONAL AURORA KINASE; EARLY EMBRYONIC-DEVELOPMENT; SMALL-MOLECULE INHIBITOR; PREVENTS TUMOR-GROWTH; DINACICLIB SCH 727965; ADVANCED SOLID TUMORS;
D O I
10.1038/nrc.2016.138
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer is characterized by uncontrolled tumour cell proliferation resulting from aberrant activity of various cell cycle proteins. Therefore, cell cycle regulators are considered attractive targets in cancer therapy. Intriguingly, animal models demonstrate that some of these proteins are not essential for proliferation of non-transformed cells and development of most tissues. By contrast, many cancers are uniquely dependent on these proteins and hence are selectively sensitive to their inhibition. After decades of research on the physiological functions of cell cycle proteins and their relevance for cancer, this knowledge recently translated into the first approved cancer therapeutic targeting of a direct regulator of the cell cycle. In this Review, we focus on proteins that directly regulate cell cycle progression (such as cyclin-dependent kinases (CDKs)), as well as checkpoint kinases, Aurora kinases and Polo-like kinases (PLKs). We discuss the role of cell cycle proteins in cancer, the rationale for targeting them in cancer treatment and results of clinical trials, as well as the future therapeutic potential of various cell cycle inhibitors.
引用
收藏
页码:93 / 115
页数:23
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