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TPX2: of spindle assembly, DNA damage response, and cancer

For more than 15 years, TPX2 has been studied as a factor critical for mitosis and spindle assembly. These functions of TPX2 are attributed to its Ran-regulated microtubule-associated protein properties and to its control of the Aurora A kinase. Overexpressed in cancers, TPX2 is being established as...

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Hauptverfasser: Neumayer, Gernot (VerfasserIn) , Belzil, Camille (VerfasserIn) , Gruss, Oliver (VerfasserIn) , Nguyen, Minh Dang (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 21 February 2014
In: Cellular and molecular life sciences
Year: 2014, Jahrgang: 71, Heft: 16, Pages: 3027-3047
ISSN:1420-9071
DOI:10.1007/s00018-014-1582-7
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/s00018-014-1582-7
Verlag, lizenzpflichtig, Volltext: https://link.springer.com/article/10.1007%2Fs00018-014-1582-7
Volltext
Verfasserangaben:Gernot Neumayer · Camille Belzil · Oliver J. Gruss · Minh Dang Nguyen

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520 |a For more than 15 years, TPX2 has been studied as a factor critical for mitosis and spindle assembly. These functions of TPX2 are attributed to its Ran-regulated microtubule-associated protein properties and to its control of the Aurora A kinase. Overexpressed in cancers, TPX2 is being established as marker for the diagnosis and prognosis of malignancies. During interphase, TPX2 resides preferentially in the nucleus where its function had remained elusive until recently. The latest finding that TPX2 plays a role in amplification of the DNA damage response, combined with the characterization of TPX2 knockout mice, open new perspectives to understand the biology of this protein. This review provides an historic overview of the discovery of TPX2 and summarizes its cytoskeletal and signaling roles with relevance to cancer therapies. Finally, the review aims to reconcile discrepancies between the experimental and pathological effects of TPX2 overexpression and advances new roles for compartmentalized TPX2. 
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