Aurora Kinase A Is Upregulated in Cutaneous T-Cell Lymphoma and Represents a Potential Therapeutic Target

  • Daniel Humme
  • , Ahmed Haider
  • , Markus Möbs
  • , Hiroshi Mitsui
  • , Mayte Suárez-Fariñas
  • , Hanako Ohmatsu
  • , Cyprienne Isabell Geilen
  • , Jürgen Eberle
  • , James G. Krueger
  • , Marc Beyer
  • , Michael Hummel
  • , Ioannis Anagnostopoulos
  • , Wolfram Sterry
  • , Chalid Assaf

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Cutaneous T-cell lymphomas (CTCLs) form a heterogeneous group of non-Hodgkin's lymphomas characterized by only poor prognosis in advanced stage. Despite significant progress made in the identification of novel genes and pathways involved in the pathogenesis of cutaneous lymphoma, the therapeutic value of these findings has still to be proven. Here, we demonstrate by gene expression arrays that Aurora kinase A is one of the highly overexpressed genes of the serine/threonine kinase in CTCL. The finding was confirmed by quantitative reverse transcriptase-PCR, western blotting, and immunohistochemistry in CTCL cell lines and primary patient samples. Moreover, treatment with a specific Aurora kinase A inhibitor blocks cell proliferation by inducing cell cycle arrest in G2 phase, as well as apoptosis in CTCL cell lines. These data provide a promising rationale for using Aurora kinase A inhibition as a therapeutic modality of CTCL.

Original languageEnglish
Pages (from-to)2292-2300
Number of pages9
JournalJournal of Investigative Dermatology
Volume135
Issue number9
DOIs
StatePublished - 18 Sep 2015
Externally publishedYes

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