European Journal of Surgical Oncology
Volume 32, Issue 10 , Pages 1093-1096, December 2006

Cox-2 expression on tissue microarray of breast cancer

  • K. Park

      Affiliations

    • Department of Pathology, Inje University, Sanggye Paik Hospital, 761-1, Sanggye-dong, Nowon-gu, Seoul 139-707, South Korea
  • ,
  • S. Han

      Affiliations

    • Department of Surgery, Inje University, Sanggye Paik Hospital, 761-1, Sanggye-dong, Nowon-gu, Seoul 139-707, South Korea
    • Corresponding Author InformationCorresponding author. Tel.: +82 2 950 1018; fax: +82 2 950 1955.
  • ,
  • E. Shin

      Affiliations

    • Department of Pathology, Inje University, Sanggye Paik Hospital, 761-1, Sanggye-dong, Nowon-gu, Seoul 139-707, South Korea
  • ,
  • H.-J. Kim

      Affiliations

    • Department of Pathology, Inje University, Sanggye Paik Hospital, 761-1, Sanggye-dong, Nowon-gu, Seoul 139-707, South Korea
  • ,
  • J.-Y. Kim

      Affiliations

    • Department of Pathology, Inje University, Sanggye Paik Hospital, 761-1, Sanggye-dong, Nowon-gu, Seoul 139-707, South Korea

Accepted 10 May 2006.

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.

Keywords: Breast cancer, Chemotherapy, Cyclooxygenase-2, Doxorubicin, Prognosis

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 This work was supported by the 2005 Inje University Research Grant.

PII: S0748-7983(06)00217-4

doi:10.1016/j.ejso.2006.05.010

European Journal of Surgical Oncology
Volume 32, Issue 10 , Pages 1093-1096, December 2006