Bibliography
- GUMIREDDY K, REDDY MV,COSENZA SC et al.: 0N01910, a non-ATP-competitive small molecule inhibitor of Plkl, is a potent anticancer agent. Cancer Cell (2005) 7(3):275–286.
- MAYER TU, KAPOOR TM, HAGGARTY SJ, KING RW, SCHREIBER SL, MITCHISON TJ: Small molecule inhibitor of mitotic spindle bipolarity identified in a phenotype-based screen. Science (1999) 286(5441):971–974.
- KEEN N, TAYLOR S: Aurora-kinase inhibitors as anticancer agents. Nat. Rev. Cancer (2004) 4(12):927–936.
- •A systematic update on the best characterised Aurora inhibitors.
- MARUMOTO T, ZHANG D, SAYA H: Aurora-A — a guardian of poles. Nat. Rev. Cancer (2005) 5(1):42–50.
- •This paper represents a good entry point in Aurora-A biology.
- MONTEMBAULT E, PRIGENT C: Aurora kinases: therapeutic potential. Drugs Fut. (2005) 30(1):29–37.
- MORTLOCK A, KEEN NJ, JUNG FH et al.: Progress in the development of selective inhibitors of Aurora kinases. Curr. Top. In Med. Chem. (2005) 5:199-213. 1180Expert Opin. Ther Patents (2005) 15(9) Recent and complete review on Aurora inhibitors.
- GLOVER DM, LEIBOWITZ MH, MCLEAN DA, PARRY H: Mutations in aurora prevent centrosome separation leading to the formation of monopolar spindles. Cell (1995) 81(1):95–105.
- ••Groundbreaking paper describing the firsttime Aurora kinase and functions.
- HU HM, CHUANG CK, LEE MJ, TSENG TC, TANG TK: Genomic organization, expression, and chromosome localization of a third aurora-related kinase gene, Aiel. DNA Cell Biol. (2000) 19(10:679–688.
- SASAI K, KATAYAMA H, STENOIEN DL et al.: Aurora-C kinase is a novel chromosomal passenger protein that can complement Aurora-B kinase function in mitotic cells. Cell Motil. Cytoskeleton (2004) 59(4):249–263.
- CARMENA M, EARNSHAW WC: The cellular geography of aurora kinases. Nat. Rev. Mol Cell Biol. (2003) 4(11):842–854.
- MARUMOTO T, HONDAS, HARA T et al.: Aurora-A kinase maintains the fidelity of early and late mitotic events in HeLa cells. J. Biol. Chem. (2003) 278(50:51786–51795.
- CASTRO A, ARLOT-BONNEMAINS Y, VIGNERON S, LABBE JC, PRIGENT C, LORCA T: APC/fizzy-related targets Aurora-A kinase for proteolysis. EMBO Rep. (2002) 3( 5):457–462.
- HIROTA T, KUNITOKU N, SASAYAMAT et al.: Aurora-A and an interacting activator, the LIM protein Ajuba, are required for mitotic commitment in human cells. Cell (2003) 114(5):585–598.
- KUFER TA, SILLJE HH, KORNER R, GRUSS 0J, MERALDI P, NIGG EA: Human TPX2 is required for targeting Aurora-A kinase to the spindle./ Cell Biol. (2002) 158(4):617–623.
- BISCHOFF JR, ANDERSON L, ZHU Y et al.: A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers. EMBO J. (1998) 17(11):3052–3065.
- ••This paper describes the two mammalianAurora-A and -B kinases and their over-expression in human colorectal tumours.
- NEBEN K, KORSHUNOV A, BENNER A et al.: Microarray-based screening for molecular markers in medulloblastoma revealed STK15 as independent predictor for survival. Cancer Res. (2004) 64(9):3103–3111.
- EWART-TOLAND A, BRIASSOULI P, DE KONING JP et al.: Identification of Stk6/STK15 as a candidate low-penetrance tumor-susceptibility gene in mouse and human. Nat. Genet. (2003) 34(0403–412.
- EGAN KM, NEWCOMB PA, AMBROSONE CB et al.: STK15 polymorphism and breast cancer risk in a population-based study. Carcinogenesis (2004) 25(10:2149–2153.
- MIAO X, SUN T, WANG Y, ZHANG X, TAN W, UN D: Functional STK15 Phe31Ile polymorphism is associated with the occurrence and advanced disease status of esophageal squamous cell carcinoma. Cancer Res. (2004) 64(8):2680–2683.
- JENG YM, PENG SY, UN CY, HSU HC: Overexpression and amplification of Aurora-A in hepatocellular carcinoma. Clin. Cancer Res. (2004) 10(6):2065–2071.
- CHEN SS, CHANG PC, CHENG YW, TANG FM, UN YS: Suppression of the STK15 oncogenic activity requires a transactivation-independent p53 function. EMBO J. (2002) 21(17):4491–4499.
- LIU Q, KANEKO S, YANG L, FELDMAN RI et al.: Aurora-A abrogation of p53 DNA binding and transactivation activity by phosphorylation of serine 215. J. Biol Chem. (2004) 279(50):52175–52182.
- KATAYAMA H, SASAI K, KAWAI H et al.: Phosphorylation by aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53. Nat. Genet. (2004) 36(1):55–62.
- CARPINELLI P, GIANELLINI L, SONCINI C et al.: Exploring the molecular mechanisms of a small molecule inhibitor of Aurora kinases. 96th Annual AACR Meeting, Anaheim: USA (2005). Astract 663.
- CASTEDO M, PERFEEIINI JL, ROUMIER T, ANDREAU K, MEDEMA R, KROEMER G: Cell death by mitotic catastrophe: a molecular definition. Oncogene (2004) 23(16):2825–2837.
- VOGEL C, KIENITZ A, HOFMANN I, MULLER R, BASTIANS H: Crosstalk of the mitotic spindle assembly checkpoint with p53 to prevent polyploidy. Oncogene (2004) 23(41):6845–6853.
- EGGERT US, KIGER AA, RICHTER C et al.: Parallel chemical genetic and genome-wide RNAi screens identify cytokinesis inhibitors and targets. PLoS. Biol (2004) 2(12):e379–.
- HATA T, F URUKAWA T, SUNAMURA M, EGAWA S, MOTOI F, OHMURA N, MARUMOTO T, SAYA H, HORII k RNA interference targeting aurora kinase a suppresses tumor growth and enhances the taxane chemosensitivity in human pancreatic cancer cells. Cancer Res. (2005) 65(7):2899–2905.
- JONKERS J, BERNS A: Oncogene addiction: sometimes a temporary slavery. Cancer Cell (2004) 6(6):535–358.
- KLEBL B: KinaTor & MasterKey: a chemoproteomics-driven medicinal chemistry approach to kinase inhibitor-based drug development. Protein kinase targets - IBC Conference, Innovations, Opportunities and Real Case Studies, Amsterdam, NE (2004).
- DITCHFIELD C, JOHNSON VI., TIGHE A et al.: Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores. J. Cell. Biol. (2003) 161(2):267–280.
- •Cellular and molecular mechanism of action of an Aurora inhibitor (ZM447439) on cells and its effects on the spindle checkpoint.
- MORTLOCK A, KEEN N, JUNG F et al.: Development of a new series of thiazolo-quinazoline inhibitors targeting Aurora kinase 95th Annual AACR Meeting. Orlando, USA (2004). Abstract 2480.
- WILKINSON RW, KEEN N, WEDGE SR et al.: Development and characterization in vivo of an inhibitor with Aurora kinase A and B specificity. 95th Annual AACR Meeting. Orlando, USA (2004). Abstract 842.
- Vertex inhibitors of Aurora-2, glycogen synthase kinase-3 and Src kinase. Expert Opin. Ther. Patent (2004) 14(3):439–443.
- GOLEC JMC: Perspectives on the discovery of VX-680, a selective inhibitor of the Aurora kinases. 229th ACS National Meeting. San Diego, USA. (2005). MEDI–307.
- HARRINGTON EA, BEBBINGTON D, MOORE J et al.: VX-680, a potent and selective small-molecule inhibitor of the Aurora kinases, suppresses tumor growth in vivo. Nat. Medicine (2004) 10(3):262–327.
- ••The first description of in vivo activity ofan Aurora inhibitor (VX-680) in animal tumour models.
- DOGGRELL SA: Dawn of Aurora kinase inhibitors as anticancer drugs. Expert Opin. Investig Drugs (2004) 13(9):1199–1201.
- FANCELLI D, BERTA D, BINDI S et al.: al Potent and Selective aurora inhibitors identified by the expansion of a novel scaffold for protein kinase inhibition. J. Med. Chem. (2005) 48(8):3080–3084.
- HAUF S, COLE RW, LATERRA S et al: The small molecule Hesperadin reveals a role for Aurora B in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint. J. Cell Biol. (2003) 161(2):281–294.
Websites
- http://www.rigel.com/rigel/oncology Rigel pipeline.
- http://www.sunesis.com/pipeline-programs.php Sunesis Programs.
- http://www.astex-technology.com/ current_portfolio.html Astex Therapeutics.
- http://www.merck.com/newsroom/ press_releases/research_and_development Merck research and development news.
- http://www.nervianoms.com Nerviano Medical Sciences.