1. Academic Validation
  2. Aurora Kinase Inhibitors: Current Status and Outlook

Aurora Kinase Inhibitors: Current Status and Outlook

  • Front Oncol. 2015 Dec 21;5:278. doi: 10.3389/fonc.2015.00278.
Vassilios Bavetsias 1 Spiros Linardopoulos 2
Affiliations

Affiliations

  • 1 Cancer Research UK Cancer Therapeutics Unit, Division of Cancer Therapeutics, The Institute of Cancer Research , London , UK.
  • 2 Cancer Research UK Cancer Therapeutics Unit, Division of Cancer Therapeutics, The Institute of Cancer Research, London, UK; Breast Cancer Now, Division of Breast Cancer Research, The Institute of Cancer Research, London, UK.
Abstract

The Aurora Kinase family comprises of cell cycle-regulated serine/threonine kinases important for mitosis. Their activity and protein expression are cell cycle regulated, peaking during mitosis to orchestrate important mitotic processes including centrosome maturation, chromosome alignment, chromosome segregation, and cytokinesis. In humans, the Aurora Kinase family consists of three members; Aurora-A, Aurora-B, and Aurora-C, which each share a conserved C-terminal catalytic domain but differ in their sub-cellular localization, substrate specificity, and function during mitosis. In addition, Aurora-A and Aurora-B have been found to be overexpressed in a wide variety of human tumors. These observations led to a number of programs among academic and pharmaceutical organizations to discovering small molecule Aurora Kinase inhibitors as anti-cancer drugs. This review will summarize the known Aurora Kinase inhibitors currently in the clinic, and discuss the current and future directions.

Keywords

aurora kinase; hematologic diseases; kinase inhibitors; neuroblastoma; small molecules.

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