S100A9 expression in invasive ductal carcinoma of the breast

• DOI: 10.1016/j.ejca.2004.01.022
• Publication Date: 2004-03-23T18:29:08Z
• Authors: K Arai; T Teratani; R Kuruto-Niwa; T Yamada; R Nozawa
• Keywords: Reverse Transcriptase Polymerase Chain Reaction; Carcinoma, Ductal, Breast; Breast Neoplasms; Adenocarcinoma; Immunohistochemistry; Neoplasm Proteins; 03 medical and health sciences; Cell Transformation, Neoplastic; 0302 clinical medicine; Cell Line, Tumor; Calgranulin B; Humans; Female; RNA, Messenger

S100A9 is associated with myelomonocytic cell differentiation and is also expressed in some epithelia. However, there have been few studies on S100A9 in adenocarcinoma (AC) because the expression in normal epithelia is limited to squamous epithelia. Our previous studies on pulmonary AC and liver carcinomas suggested that S100A9 expression in carcinomas of glandular cell origin is related to poor tumour differentiation. In this study, we examined S100A9 expression in invasive breast carcinoma and evaluated the relation of the expression to the tumour differentiation in 70 cases of invasive ductal carcinoma (IDC) of the breast. S100A9 gene and protein expression was detected in MCF-7 breast carcinoma cells. The rate of S100A9 immunopositivity in IDC showed a higher correlation with poor tumour differentiation, especially in nuclear pleomorphism (P=0.0002) and mitotic activity (P=0.0001). Furthermore, transcriptional expression of S100A9 in sections of IDC could be detected in cases with a high S100A9 immunopositivity. No significant differences in the number of myelomonocytic cells expressing S100A9 were found among cases. There was no correlation between S100A9 immunopositivity and lymph node metastasis (P=0.32). S100A9 immunopositivity in non-invasive ductal carcinoma was also associated with poor tumour differentiation. No immunopositive reaction was observed in invasive lobular carcinomas with a classic cytological appearance and non-neoplastic duct cells. We conclude that S100A9 in glandular epithelial cells is newly expressed under cancerous conditions and is over-expressed in poorly differentiated AC.