Correlation of COX-2 and ciclyn D-1 after short-time neoadjuvant tamoxifen on breast cancer

Authors

  • Eduardo C. Millen isciplina de Mastologia, Departamento de Ginecologia da Universidade Federal de São Paulo (Unifesp). Faculdade de Medicina de Volta Redonda (UniFOA), Volta Redonda, Rio de Janeiro, RJ.
  • Marcelo Madeira isciplina de Mastologia, Departamento de Ginecologia da Universidade Federal de São Paulo (Unifesp). Centro de Referência da Saúde da Mulher (CRSM), Hospital Pérola Byington, São Paulo. SP.
  • Angela F. Logullo Waitzberg Departamento de Patologia da Universidade Federal de São Paulo (Unifesp).
  • Fernando A. Soares Departamento de Patologia da Fundação Antônio Prudente, Hospital A. C. Camargo, São Paulo, SP.
  • Cyntia Osório Departamento de Patologia da Fundação Antônio Prudente, Hospital A. C. Camargo, São Paulo, SP.
  • Suely Nonogaki Divisão Técnica de Patologia, Instituto Adolfo Lutz, São Paulo, SP.
  • Luiz H. Gebrim Disciplina de Mastologia, Departamento de Ginecologia da Universidade Federal de São Paulo (Unifesp). Centro de Referência da Saúde da Mulher (CRSM), Hospital Pérola Byington, São Paulo. SP.

Keywords:

COX-2, Ciclyn D-1, Tamoxifen, Breast cancer

Abstract

Introduction: Tamoxifen is the most used drug in the hormonal therapy of the breast cancer. Ciclyn D-1,
one CCNDI gene product's (PRADI), is essential for the normal lobule-alveolar mammary development
and acts in the cellular cycle control. Ciclyn D-1 superexpression act negatively in tamoxifen treatment,and may contribute to predict the failure observed in some patients. COX-2 activity induces oestrogen oxidation to dietilstilbestrol and promotes genotoxics effects on the breast. Ciclyn D-1 and COX-2 association
had not been described yet to short time tamoxifen treatment. Objective: Evaluate short time (14 days)
neaodjuvant tamoxifen effects on COX-2 and ciclyn D-1 expression in breast cancer patients. Methods:
Randomized prospective study in the Federal University of Sao Paulo. Twenty five patients with stage II
and III breast cancer were included. The groups were control (n = 13) and treatment (n = 12). Ciclyn
D-1 and COX-2 samples were evaluated before and after treatment. Imunohistochemistry was performed
on the tissue sections using a polyclonal antibody to COX-2 (Novocastra - Clone 4H12) and cyclin D-1
(Novocastra – Clone DCS-6). The results were classified according Already score, based on the intensity
and fraction marked cells. Results: COX-2 was positive in 56% of tumors. No significant difference was
observed between the two groups (p = 0.39 Mann Whitney test). The Difference of cyclin D-1 medium
(post - pre) in the control group was 5, while in the tamoxifen group was 0.5. (p = 0.08, Mann Whitney
test). Correlation between COX-2 and ciclyn D-1 was expressed by Pearson index (r). In treatment group
moderate linear and positive correlation was observed (r = 0.51 – Pearson's index) (p = 0.08). It wasn't
observed in control group (r = 0.42) (p = 0.12). Conclusion: Tamoxifen treatment in short time period
(14 days) wasn't modified significantly COX-2 and ciclyn D-1 expression.

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Published

2026-07-27

How to Cite

Millen, E. C., Madeira, M., Waitzberg, A. F. L., Soares, F. A., Osório, C., Nonogaki, S., & Gebrim, L. H. (2026). Correlation of COX-2 and ciclyn D-1 after short-time neoadjuvant tamoxifen on breast cancer. Mastology, 19(2). Retrieved from https://mastology.org/journal/article/view/2040

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