Literature DB >> 18377825

Tubulin-associated proteins: Aurora and Polo-like kinases as therapeutic targets in cancer.

Steven L Warner1, Bret J Stephens, Daniel D Von Hoff.   

Abstract

Tubulin is a very important target for cancer-fighting therapies; therefore, the cancer research community continues to adopt new ways of developing the therapeutic potential of tubulin and tubulin-associated proteins. Two families of tubulin-associated kinases, Aurora and Polo-like, have received significant attention regarding how they contribute to tumorigenesis and can be targeted with selective small molecule inhibitors. Aurora and Polo-like kinases play essential roles in centrosome separation, chromosome alignment and segregation, and cytokinesis. Inhibition of any of these kinases results in abnormal mitotic events (which vary depending on the particular family member) and eventually leads to apoptosis. Because of the biological consequences of inhibiting these kinases, several Aurora or Polo-like selective inhibitors have advanced to various stages of preclinical and clinical development; the most advanced are currently in phase 2 clinical trials.

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Year:  2008        PMID: 18377825     DOI: 10.1007/s11912-008-0020-0

Source DB:  PubMed          Journal:  Curr Oncol Rep        ISSN: 1523-3790            Impact factor:   5.075


  44 in total

1.  Aurora kinase inhibitor ZM447439 blocks chromosome-induced spindle assembly, the completion of chromosome condensation, and the establishment of the spindle integrity checkpoint in Xenopus egg extracts.

Authors:  Bedrick B Gadea; Joan V Ruderman
Journal:  Mol Biol Cell       Date:  2004-12-22       Impact factor: 4.138

2.  MLN8054, a small-molecule inhibitor of Aurora A, causes spindle pole and chromosome congression defects leading to aneuploidy.

Authors:  Kara Hoar; Arijit Chakravarty; Claudia Rabino; Deborah Wysong; Douglas Bowman; Natalie Roy; Jeffrey A Ecsedy
Journal:  Mol Cell Biol       Date:  2007-04-16       Impact factor: 4.272

3.  A putative serine/threonine kinase encoding gene BTAK on chromosome 20q13 is amplified and overexpressed in human breast cancer cell lines.

Authors:  S Sen; H Zhou; R A White
Journal:  Oncogene       Date:  1997-05-08       Impact factor: 9.867

4.  Discovery, synthesis, and in vivo activity of a new class of pyrazoloquinazolines as selective inhibitors of aurora B kinase.

Authors:  Andrew A Mortlock; Kevin M Foote; Nicola M Heron; Frédéric H Jung; Georges Pasquet; Jean-Jacques M Lohmann; Nicolas Warin; Fabrice Renaud; Chris De Savi; Nicola J Roberts; Trevor Johnson; Cyril B Dousson; George B Hill; David Perkins; Glenn Hatter; Robert W Wilkinson; Stephen R Wedge; Simon P Heaton; Rajesh Odedra; Nicholas J Keen; Claire Crafter; Elaine Brown; Katherine Thompson; Stephen Brightwell; Liz Khatri; Madeleine C Brady; Sarah Kearney; David McKillop; Steve Rhead; Tony Parry; Stephen Green
Journal:  J Med Chem       Date:  2007-03-21       Impact factor: 7.446

5.  ON01910, a non-ATP-competitive small molecule inhibitor of Plk1, is a potent anticancer agent.

Authors:  Kiranmai Gumireddy; M V Ramana Reddy; Stephen C Cosenza; R Boominathan; R Boomi Nathan; Stacey J Baker; Nabisa Papathi; Jiandong Jiang; James Holland; E Premkumar Reddy
Journal:  Cancer Cell       Date:  2005-03       Impact factor: 31.743

6.  Proteomic screen finds pSer/pThr-binding domain localizing Plk1 to mitotic substrates.

Authors:  Andrew E H Elia; Lewis C Cantley; Michael B Yaffe
Journal:  Science       Date:  2003-02-21       Impact factor: 47.728

Review 7.  Differential regulation of polo-like kinase 1, 2, 3, and 4 gene expression in mammalian cells and tissues.

Authors:  Jeffrey A Winkles; Gregory F Alberts
Journal:  Oncogene       Date:  2005-01-10       Impact factor: 9.867

8.  AZD1152, a selective inhibitor of Aurora B kinase, inhibits human tumor xenograft growth by inducing apoptosis.

Authors:  Robert W Wilkinson; Rajesh Odedra; Simon P Heaton; Stephen R Wedge; Nicholas J Keen; Claire Crafter; John R Foster; Madeleine C Brady; Alison Bigley; Elaine Brown; Kate F Byth; Nigel C Barrass; Kirsten E Mundt; Kevin M Foote; Nicola M Heron; Frederic H Jung; Andrew A Mortlock; F Thomas Boyle; Stephen Green
Journal:  Clin Cancer Res       Date:  2007-06-15       Impact factor: 12.531

9.  The mitotic serine threonine kinase, Aurora-2, is a potential target for drug development in human pancreatic cancer.

Authors:  Sangeeta Rojanala; Haiyong Han; Rubén M Muñoz; Walden Browne; Raymond Nagle; Daniel D Von Hoff; David J Bearss
Journal:  Mol Cancer Ther       Date:  2004-04       Impact factor: 6.261

10.  Antitumor activity of MLN8054, an orally active small-molecule inhibitor of Aurora A kinase.

Authors:  Mark G Manfredi; Jeffrey A Ecsedy; Kristan A Meetze; Suresh K Balani; Olga Burenkova; Wei Chen; Katherine M Galvin; Kara M Hoar; Jessica J Huck; Patrick J LeRoy; Emily T Ray; Todd B Sells; Bradley Stringer; Stephen G Stroud; Tricia J Vos; Gabriel S Weatherhead; Deborah R Wysong; Mengkun Zhang; Joseph B Bolen; Christopher F Claiborne
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-23       Impact factor: 11.205

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  10 in total

1.  Anaphase catastrophe is a target for cancer therapy.

Authors:  Fabrizio Galimberti; Sarah L Thompson; Saranya Ravi; Duane A Compton; Ethan Dmitrovsky
Journal:  Clin Cancer Res       Date:  2011-02-02       Impact factor: 12.531

2.  Role of senescence and mitotic catastrophe in cancer therapy.

Authors:  Richa Singh; Jasmine George; Yogeshwer Shukla
Journal:  Cell Div       Date:  2010-01-21       Impact factor: 5.130

Review 3.  Factors underlying sensitivity of cancers to small-molecule kinase inhibitors.

Authors:  Pasi A Jänne; Nathanael Gray; Jeff Settleman
Journal:  Nat Rev Drug Discov       Date:  2009-07-24       Impact factor: 84.694

4.  Meta-analysis of Aurora Kinase A (AURKA) Expression Data Reveals a Significant Correlation Between Increased AURKA Expression and Distant Metastases in Human ER-positive Breast Cancers.

Authors:  Heinz-Ulli G Weier; Jian-Hua Mao
Journal:  J Data Mining Genomics Proteomics       Date:  2013-03-06

5.  A genetic variant of Aurora kinase A promotes genomic instability leading to highly malignant skin tumors.

Authors:  Enrique C Torchia; Yiyun Chen; Hong Sheng; Hiroshi Katayama; James Fitzpatrick; William R Brinkley; Carlos Caulin; Subrata Sen; Dennis R Roop
Journal:  Cancer Res       Date:  2009-09-08       Impact factor: 12.701

6.  The novel Aurora A kinase inhibitor MLN8237 is active in resistant chronic myeloid leukaemia and significantly increases the efficacy of nilotinib.

Authors:  Kevin R Kelly; Jeffrey Ecsedy; Ernest Medina; Devalingam Mahalingam; Swaminathan Padmanabhan; Steffan T Nawrocki; Francis J Giles; Jennifer S Carew
Journal:  J Cell Mol Med       Date:  2011-10       Impact factor: 5.310

7.  Pan Aurora Kinase Inhibitor: A Promising Targeted-Therapy in Dedifferentiated Liposarcomas With Differential Efficiency Depending on Sarcoma Molecular Profile.

Authors:  Jean Camille Mattei; Corinne Bouvier-Labit; Doriane Barets; Nicolas Macagno; Mathieu Chocry; Frédéric Chibon; Philippe Morando; Richard Alexandre Rochwerger; Florence Duffaud; Sylviane Olschwang; Sébastien Salas; Carine Jiguet-Jiglaire
Journal:  Cancers (Basel)       Date:  2020-03-03       Impact factor: 6.639

8.  Fission yeast Scp3 potentially maintains microtubule orientation through bundling.

Authors:  Kanako Ozaki; Yuji Chikashige; Yasushi Hiraoka; Tomohiro Matsumoto
Journal:  PLoS One       Date:  2015-03-13       Impact factor: 3.240

Review 9.  Aurora Kinases and Potential Medical Applications of Aurora Kinase Inhibitors: A Review.

Authors:  Paschalis Gavriilidis; Alexandros Giakoustidis; Dimitrios Giakoustidis
Journal:  J Clin Med Res       Date:  2015-08-23

10.  MLN-8237: A dual inhibitor of aurora A and B in soft tissue sarcomas.

Authors:  Jayasree S Nair; Gary K Schwartz
Journal:  Oncotarget       Date:  2016-03-15
  10 in total

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