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Aurora A overexpression in breast cancer patients induces taxane resistance and results in worse prognosis

J BUON. 2015 Nov-Dec;20(6):1414-9.

Abstract

Purpose: The aim of this study was to determine the expression level of Aurora A in human breast cancer tissues and to test whether there is a relationship between its expression levels and clinicopathological parameters including response to taxanes, tumor grade, estrogen receptor (ER) status, human epidermal growth factor receptor 2 (HER2) status, and overall survival (OS).

Methods: We retrospectively analyzed paraffin-embedded tissue sections from 49 metastatic breast cancer patients whose clinical outcomes had been tracked after taxane treatment. The expression status of Aurora A was defined by immunohistochemistry (IHC) using the anti-Aurora A antibody.

Results: Aurora A was overexpressed in 73% of the examined specimens. There was significant correlation between high Aurora A expression and decreased taxane sensitivity (p=0.02). There was no association between the clinicopathological parameters including histologic grade, ER positivity and triple negative molecular subtype and the level of Aurora A expression. However, HER2 positive tumors showed significantly higher Aurora A expression compared with HER2 negative tumors (p=0.02). Kaplan-Meier survival analysis failed to show a significant correlation between expression levels of Aurora A and OS although patients with low Aurora A levels had a marginally longer survival compared to patients with high levels.

Conclusion: Our data suggest that Aurora A may be a promising predictive and prognostic marker in patients with breast cancer.

MeSH terms

  • Aurora Kinase A / analysis
  • Aurora Kinase A / physiology*
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / enzymology*
  • Breast Neoplasms / mortality
  • Bridged-Ring Compounds / therapeutic use*
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Prognosis
  • Receptor, ErbB-2 / analysis
  • Retrospective Studies
  • Taxoids / therapeutic use*

Substances

  • Bridged-Ring Compounds
  • Taxoids
  • taxane
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • AURKA protein, human
  • Aurora Kinase A