Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/74143
Title: Expression of maspin in mammary gland tumors of the dog
Authors: Espinosa de los Monteros, A. 
Millán, M. Y.
Ramírez, G. A.
Ordás, J.
Reymundo, C.
Martín de las Mulas, J.
UNESCO Clasification: 310907 Patología
Keywords: Dogs
Immunohistochemistry
Mammary Gland
Maspin
Myoepithelium
Issue Date: 2005
Journal: Veterinary Pathology 
Abstract: Maspin is a serine protease inhibitor that inhibits tumor invasion and metastasis in human breast cancer and is consistently expressed by mammary myoepithelial cells (MECs). To analyze the value of maspin as a marker of the MEC layer of the normal and tumoral canine mammary gland, the immunohistochemical expression of maspin was studied in formalin-fixed tissues from 55 benign and malignant tumors (40 tumors also contained the surrounding normal mammary gland) using a commercially available monoclonal antibody. Periacinar and periductal MECs of all 40 normal mammary glands were stained by the anti-human maspin monoclonal antibody, and immunoreactivity was observed in the nucleus and cytoplasm of these cells. In addition, maspin was found in 53 (98%) of the tumors studied, reacting with the MECs in 100% of benign tumors and 93% of malignant tumors and to the epithelia] cells of 16% of benign and 73% of malignant tumors. In the MEC compartment, immunoreactivity was observed in the cytoplasm of hypertrophic MECs, fusiform MECs, stellate MECs, rounded (myoepithelial) cells, and chondroblasts. In the epithelial cell compartment, immunoreactivity was observed in the cytoplasm of cells with and without squamous differentiation. Stromal myofibroblasts were unreactive. Maspin appears to be a very sensitive marker of the normal and neoplastic myoepithelium that, contrary to smooth muscle differentiation markers, does not stain stromal myofibroblasts. In addition, a subset of neoplastic epithelial cells reacted with the maspin antibody. The relationship between maspin expression in different cellular compartments of canine mammary carcinomas and the biologic aggressiveness of the disease remains to be elucidated.
URI: http://hdl.handle.net/10553/74143
ISSN: 0300-9858
DOI: 10.1354/vp.42-3-250
Source: Veterinary Pathology [ISSN 0300-9858], v. 42 (3), p. 250-257, (Mayo 2005)
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