Cox-2 expression on tissue microarray of breast cancer

Eur J Surg Oncol. 2006 Dec;32(10):1093-6. doi: 10.1016/j.ejso.2006.05.010. Epub 2006 Jun 21.

Abstract

Aim: To measure cyclooxygenase-2 (Cox-2) expression in a series of breast cancers and evaluate its potential as a predictive marker for doxorubicin chemotherapy.

Patients and methods: Cox-2 expression was analyzed in 178 node-positive patients treated with doxorubicin-based adjuvant chemotherapy by immunohistochemistry on tissue microarray (TMA).

Results: Cox-2 was over-expressed in 70 out of the 178 invasive breast cancers. Cox-2 expression was significantly increased in undifferentiated tumors. There was no significant association between Cox-2 over-expression and tumor size, histologic grade, and estrogen receptor expression. Disease-free survival and overall survival of the patients having Cox-2 expressing tumor were significantly decreased when compared with the patients having Cox-2 negative tumor (p=0.009 for DFS, p=0.011 for OS).

Conclusion: Cox-2 expression may represent an aggressive phenotype of breast cancer which is resistant to doxorubicin.

MeSH terms

  • Antibiotics, Antineoplastic / therapeutic use
  • Axilla
  • Breast Neoplasms / enzymology*
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Breast Neoplasms / therapy
  • Chemotherapy, Adjuvant
  • Cyclooxygenase 2 / metabolism*
  • Disease-Free Survival
  • Doxorubicin / therapeutic use
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis
  • Mastectomy, Radical
  • Middle Aged
  • Phenotype
  • Survival Rate
  • Tissue Array Analysis*

Substances

  • Antibiotics, Antineoplastic
  • Doxorubicin
  • Cyclooxygenase 2