4.3 Article

Cyclo-oxygenase type 2 is dysregulated in breast ductal carcinoma in situ and correlates with poor outcome

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejogrb.2010.02.033

Keywords

Breast; Cyclo-oxygenase type-2 (COX-2); Ductal Carcinoma in situ (DCIS); Microinvasive carcinoma of the breast (MICB); Prognosis

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Objective: Clinico-pathologic data on microinvasive carcinoma of the breast (MICB) as defined by the 2003 TNM criteria (T1mic <= 1 mm) are scarce. Nowadays, we do not know the percentages of Ductal Carcinoma in situ (DCIS) that will progress to invasion and predictive markers are not available. Cyclooxygenase type-2 (COX-2) is overexpressed in many human malignant tumours and has been linked to the processes of carcinogenesis, cell survival, invasion and metastasis. Despite the data on elevated COX-2 expression in breast neoplasia, the mechanism of upregulation remains unclear. This study aims to evaluate COX-2 expression in DCIS in comparison to MICB in order to establish the importance of this marker as a predictor of microinvasion and the correlation with Van Nuys classification. Study design: A retrospective study was performed on archival paraffin-embedded formalin-fixed tissue samples of DOS and MICB from women who had undergone surgery. The COX-2 expression was assayed by immunohistochemistry using a specific polyclonal anti-human COX-2 antibody. Expression was scored in a scale 0 (absent) to 4 (strong) based on the extent and intensity of tumour cell staining. Results: Fifty-two cases of DCIS and 40 of MICB were studied. In all cases. COX-2 was detected in the cytoplasm of tumour cells, and elevated COX-2 expression was observed in Van Nuys high-grade CDIS cases compared with low and intermediate grades (p < 0.05). In addition, enhanced COX-2 expression was significantly higher in DCIS component from MICB patients (82% cases) than in DCIS pure patients (40.4%) (p < 0.05). In a multivariate model which includes age, tumour size, mammography, histological grade and COX-2 expression, we found COX-2 positivity to be an independent factor for microinvasion (OR 3.90; 95% Cl 1.88-14.3). Conclusions: COX-2 is associated to higher Van Nuys grades of breast CDIS, and could be a molecular marker to identify the cases of DCIS which could progress to MICB. Condensation: COX-2 as a molecular marker in microinvasive carcinoma of the breast. (C) 2010 Elsevier Ireland Ltd. All rights reserved.

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