Overexpression of Galectin-7, A Myoepithelial Cell Marker, Enhances Spontaneous Metastasis of Breast Cancer Cells

被引:73
|
作者
Demers, Melanie [1 ]
Rose, April A. N. [2 ]
Grosset, Andree-Anne [3 ]
Biron-Pain, Katherine [1 ]
Gaboury, Louis [3 ]
Siegel, Peter M. [2 ]
St-Pierre, Yves [1 ]
机构
[1] Univ Quebec, Inst Armand Frappier, INRS, Laval, PQ H7V 1B7, Canada
[2] McGill Univ, Goodman Canc Ctr, Montreal, PQ, Canada
[3] Inst Rech Immunol & Cancerol, Montreal, PQ, Canada
来源
AMERICAN JOURNAL OF PATHOLOGY | 2010年 / 176卷 / 06期
关键词
CYTOCHROME-C RELEASE; GENE-EXPRESSION; MOLECULAR PORTRAITS; APOPTOSIS; TUMOR; MODEL; BONE; DISSEMINATION; PROGRESSION; GROWTH;
D O I
10.2353/ajpath.2010.090876
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Galectins are members of a family of beta-galactosidesbinding proteins that have recently emerged as novel modulators in different aspects of cancer. The expression of galectins in tumors and/or the tissue surrounding them has been well documented. Since galectin-7 expression has been associated with epithelial tissues and varies significantly in various types of cancer, we have investigated for the first time its role in breast cancer. Using two preclinical mouse models, high levels of galectin-7 expression in breast cancer cells drastically increased their ability to metastasize to lungs and bones. Significant increases in the number of pulmonary metastases and osteolytic lesions were induced by overexpression of galectin-7 compared with control cells. In human tissues, galectin-7 was specifically found in myoepithelial cells of normal human breast tissue, but not in luminal cells. Its expression was severely altered in breast carcinoma, many samples showing greater than 70% of galectin-7 positive cells. High expression levels of galectin-7 were restricted to high-grade breast carcinomas, including HER2 overexpressing and basal-like groups. In HER2 overexpressing cases, galectin-7 expression was associated with lymph node axillary metastasis. Taken together, our results indicate that galectin-7 may represent a potential target for both specific detection and therapeutic inhibition of metastatic breast cancer. (Am J Pathol 2010, 176:3023-3031; 10.2353/ajpath.2010.090876)
引用
收藏
页码:3023 / 3031
页数:9
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