Cyclooxygenase-2 expression in primary breast cancers predicts dissemination of cancer cells to the bone marrow

  • Anthony Lucci
  • Savitri Krishnamurthy
  • Balraj Singh
  • Isabelle Bedrosian
  • Funda Meric-Bernstam
  • James Reuben
  • Kristine Broglio
  • Kailash Mosalpuria
  • Ashutosh Lodhi
  • Laura Vincent
  • Massimo Cristofanilli
Clinical Trial

DOI: 10.1007/s10549-008-0135-x

Cite this article as:
Lucci, A., Krishnamurthy, S., Singh, B. et al. Breast Cancer Res Treat (2009) 117: 61. doi:10.1007/s10549-008-0135-x

Abstract

Purpose Cyclooxygenase-2 (COX2) plays a role in breast cancer progression at various stages starting from pre-malignant phenotype to clinical metastasis. Breast cancer metastasizes commonly to the bone and preclinical studies suggest an involvement of COX2 in this process. Detection of disseminated tumor cells in the bone marrow of patients at the time of surgery correlates with the subsequent development of clinical bone metastasis. Therefore, to investigate whether COX2 is important for breast cancer metastasis in humans, we analyzed COX2 protein expression by immunostaining of primary tumors from 112 operable stages I, II, or III patients and determined its correlation with bone marrow micrometastasis (BMM). Methods We detected COX2 protein in primary tumors by immunostaining with a monoclonal antibody, and tumor cells present in the bone marrow by immunostaining for epithelial cytokeratins and by morphological criteria. Results COX2 expression in primary breast cancer correlated with BMM in a highly statistically significant manner (P = 0.006). Our statistical analyses of correlations of the COX2 positivity in primary tumor with other clinically relevant indicators revealed that COX2 positivity correlates with high nuclear grade (P = 0.0004). Furthermore, we were able to detect COX2 protein in BMM by immunostaining. Conclusions These studies indicate that COX2 produced in primary breast cancer cells may be vital to the initial development of BMM that may subsequently lead to osteolytic bone metastases in patients with breast cancer, and that COX2 inhibitors may be useful in halting this process.

Keywords

Breast cancer COX2 Bone marrow micrometastasis Disseminated tumor cells Minimal residual disease 

Copyright information

© Springer Science+Business Media, LLC. 2008

Authors and Affiliations

  • Anthony Lucci
    • 1
    • 2
  • Savitri Krishnamurthy
    • 2
    • 3
  • Balraj Singh
    • 1
    • 2
  • Isabelle Bedrosian
    • 1
  • Funda Meric-Bernstam
    • 1
  • James Reuben
    • 2
    • 4
  • Kristine Broglio
    • 5
  • Kailash Mosalpuria
    • 1
  • Ashutosh Lodhi
    • 1
  • Laura Vincent
    • 1
  • Massimo Cristofanilli
    • 2
    • 6
  1. 1.Department of Surgical Oncology, Unit 444The University of Texas M.D. Anderson Cancer CenterHoustonUSA
  2. 2.Advanced Research Center for Microscopic DiseaseThe University of Texas M.D. Anderson Cancer CenterHoustonUSA
  3. 3.Department of PathologyThe University of Texas M.D. Anderson Cancer CenterHoustonUSA
  4. 4.Department of HematopathologyThe University of Texas M.D. Anderson Cancer CenterHoustonUSA
  5. 5.Department of Quantitative SciencesThe University of Texas M.D. Anderson Cancer CenterHoustonUSA
  6. 6.Department of Breast Medical OncologyThe University of Texas M.D. Anderson Cancer CenterHoustonUSA

Personalised recommendations