Aurora kinase inhibitor patents and agents in clinical testing: an update (2009-10)

被引:36
作者
Cheung, Chun Hei Antonio [2 ]
Coumar, Mohane Selvaraj [3 ]
Chang, Jang-Yang [2 ]
Hsieh, Hsing-Pang [1 ]
机构
[1] Natl Hlth Res Inst, Inst Biotechnol & Pharmaceut Res, Zhunan Town 350, Miaoli County, Taiwan
[2] Natl Hlth Res Inst, Natl Inst Canc Res, Tainan 70456, Taiwan
[3] Pondicherry Univ, Ctr Bioinformat, Sch Life Sci, Kalapet 605014, Puducherry, India
关键词
AMG; 900; AT-9283; aurora kinase inhibitors; AZD1152; BI811283; CYC116; ENMD-2076; GSK1070916; MLN8054; MLN8237; PF-3814735; PHA739358; R763; SNS-314; VX-680/MK0457; VX-689/MK-5108; XL228; SMALL-MOLECULE INHIBITOR; CELL LUNG-CARCINOMA; B-KINASE; SELECTIVE INHIBITOR; ANTITUMOR-ACTIVITY; IN-VITRO; FREQUENT OVEREXPRESSION; CANCER-CELLS; WILD-TYPE; BCR-ABL;
D O I
10.1517/13543776.2011.574614
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Mitosis is a key step in the cell cycle and is controlled by several cell cycle regulators, including aurora kinases. Aurora family members A, B and C are essential for spindle assembly, centrosome maturation, chromosomal segregation and cytokinesis. Overexpression/amplification of aurora kinases has been implicated in oncogenic transformation, including the development of chromosomal instability in cancer cells. Hence, the use of aurora kinase small molecule inhibitors as a potential molecular-targeted therapeutic intervention for cancer is being pursued by various researchers. Area covered: This review provides an update on aurora kinase inhibitors based on developments from 2009 to 2010. The medicinal chemistry aspects of aurora kinase inhibitors, with a particular emphasis on the patent literature, are reviewed. Databases such as PubMed, SCOPUS (R), Scifinder (R) and www.clinicaltrials.gov database were used to search for literature in the preparation of this review. Expert opinion: Around a dozen aurora kinase inhibitors are currently undergoing various Phase I - II evaluations for different human cancers. Instead of being applied as a monotherapy, combinations of aurora kinase inhibitors and existing chemotherapeutic compounds seem to give better therapeutic outcomes and are, therefore, a promising future cancer therapy.
引用
收藏
页码:857 / 884
页数:28
相关论文
共 98 条
[31]   The Aurora kinase inhibitor VX-680 induces endoreduplication and apoptosis preferentially in cells with compromised p53-dependent postmitotic checkpoint function [J].
Gizatullin, Farid ;
Yao, Yao ;
Kung, Victor ;
Harding, Matthew W. ;
Loda, Massimo ;
Shapiro, Geoffrey I. .
CANCER RESEARCH, 2006, 66 (15) :7668-7677
[32]   Anovel Aurora-A kinase inhibitor MLN8237 induces cytotoxicity and cell-cycle arrest in multiple myeloma [J].
Goerguen, Guellue ;
Calabrese, Elisabetta ;
Hideshima, Teru ;
Ecsedy, Jeffrey ;
Perrone, Giulia ;
Mani, Mala ;
Ikeda, Hiroshi ;
Bianchi, Giada ;
Hu, Yiguo ;
Cirstea, Diana ;
Santo, Loredana ;
Tai, Yu-Tzu ;
Nahar, Sabikun ;
Zheng, Mei ;
Bandi, Madhavi ;
Carrasco, Ruben D. ;
Raje, Noopur ;
Munshi, Nikhil ;
Richardson, Paul ;
Anderson, Kenneth C. .
BLOOD, 2010, 115 (25) :5202-5213
[33]  
Gürtler U, 2010, J CLIN ONCOL, V28
[34]   Antineoplastic effects of an Aurora B kinase inhibitor in breast cancer [J].
Gully, Christopher P. ;
Zhang, Fanmao ;
Chen, Jian ;
Yeung, James A. ;
Velazquez-Torres, Guermarie ;
Wang, Edward ;
Yeung, Sai-Ching Jim ;
Lee, Mong-Hong .
MOLECULAR CANCER, 2010, 9
[35]   Identification of genes that confer tumor cell resistance to the Aurora B kinase inhibitor, AZD1152 [J].
Guo, J. ;
Anderson, M. G. ;
Tapang, P. ;
Palma, J. P. ;
Rodriguez, L. E. ;
Niquette, A. ;
Li, J. ;
Bouska, J. J. ;
Wang, G. ;
Semizarov, D. ;
Albert, D. H. ;
Donawho, C. K. ;
Glaser, K. B. ;
Shah, O. J. .
PHARMACOGENOMICS JOURNAL, 2009, 9 (02) :90-102
[36]   GSK1070916, a potent Aurora B/C kinase inhibitor with broad antitumor activity in tissue culture cells and human tumor xenograft models [J].
Hardwicke, Mary Ann ;
Oleykowski, Catherine A. ;
Plant, Ramona ;
Wang, Jamin ;
Liao, Qiaoyin ;
Moss, Katherine ;
Newlander, Ken ;
Adams, Jerry L. ;
Dhanak, Dashyant ;
Yang, Jingsong ;
Lai, Zhihong ;
Sutton, David ;
Patrick, Denis .
MOLECULAR CANCER THERAPEUTICS, 2009, 8 (07) :1808-1817
[37]   VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo [J].
Harrington, EA ;
Bebbington, D ;
Moore, J ;
Rasmussen, RK ;
Ajose-Adeogun, AO ;
Nakayama, T ;
Graham, JA ;
Demur, C ;
Hercend, T ;
Diu-Hercend, A ;
Su, M ;
Golec, JMC ;
Miller, KM .
NATURE MEDICINE, 2004, 10 (03) :262-267
[38]   MLN8054, a small-molecule inhibitor of Aurora A, causes spindle pole and chromosome congression defects leading to aneuploidy [J].
Hoar, Kara ;
Chakravarty, Arijit ;
Rabino, Claudia ;
Wysong, Deborah ;
Bowman, Douglas ;
Roy, Natalie ;
Ecsedy, Jeffrey A. .
MOLECULAR AND CELLULAR BIOLOGY, 2007, 27 (12) :4513-4525
[39]   Fragment-Based Discovery of the Pyrazol-4-yl Urea (AT9283), a Multitargeted Kinase Inhibitor with Potent Aurora Kinase Activity [J].
Howard, Steven ;
Berdini, Valerio ;
Boulstridge, John A. ;
Carr, Maria G. ;
Cross, David M. ;
Curry, Jayne ;
Devine, Lindsay A. ;
Early, Theresa R. ;
Fazal, Lynsey ;
Gill, Adrian L. ;
Heathcote, Michelle ;
Maman, Sarita ;
Matthews, Julia E. ;
McMenamin, Rachel L. ;
Navarro, Eva F. ;
O'Brien, Michael A. ;
O'Reilly, Marc ;
Rees, David C. ;
Reule, Matthias ;
Tisi, Dominic ;
Williams, Glyn ;
Vinkovic, Mladen ;
Wyatt, Paul G. .
JOURNAL OF MEDICINAL CHEMISTRY, 2009, 52 (02) :379-388
[40]   MLN8054, an Inhibitor of Aurora A Kinase, Induces Senescence in Human Tumor Cells Both In vitro and In vivo [J].
Huck, Jessica J. ;
Zhang, Mengkun ;
McDonald, Alice ;
Bowman, Doug ;
Hoar, Kara M. ;
Stringer, Bradley ;
Ecsedy, Jeffery ;
Manfredi, Mark G. ;
Hyer, Marc L. .
MOLECULAR CANCER RESEARCH, 2010, 8 (03) :373-384