Abstract | AIM: The aim of the present study was to evaluate E-cadherin, whose expression remains poorly understood in the intercellular adhesion of metastatic breast cancer cells in bone, the most prevalent site for metastatic growth. MATERIALS AND METHODS: An immunohistochemical staining method was used for the localization of E-cadherin protein in tissue biopsy specimens of normal breast (n = 9) and well- (n = 8), moderately (n = 8) or poorly (n = 14) differentiated invasive primary breast cancer and metastatic breast cancer in bone (n = 17). The expression patterns of E-cadherin were classified as homogeneous (most cells exhibiting positivity), heterogeneous (a few scattered patches of cells with positivity) or negative (cells with undetectable positivity). RESULTS: Normal breast epithelial cells showed homogeneous overexpression of E-cadherin in all cases. A progressive and statistically significant reduction of E-cadherin expression was detected in the histologically well- to moderately to poorly differentiated breast cancer cells (p < 0.001). The clumps of invasive primary breast cancer cells in CD-31-positive blood vessels exhibited E-cadherin expression. Moreover, as compared to the poorly differentiated breast cancer cells, a significantly increased frequency of the metastatic breast cancer cells in bone exhibited homogeneous expression of E-cadherin in 15 out of 17 and heterogeneous expression in the remaining 2 cases (McNemar Exact p < 0.001). This is the first demonstration of membranous overexpression of E-cadherin on metastatic breast cancer cells in bone; the high frequency of its expression may have a role in the intercellular adhesion of metastatic cells in bone.
|
Authors | Baisakhi Saha, Benjaporn Chaiwun, Sarah S Imam, Denice D Tsao-Wei, Susan Groshen, Wesley Y Naritoku, S Ashraf Imam |
Journal | Anticancer research
(Anticancer Res)
2007 Nov-Dec
Vol. 27
Issue 6B
Pg. 3903-8
ISSN: 0250-7005 [Print] Greece |
PMID | 18225549
(Publication Type: Journal Article)
|
Chemical References |
|
Topics |
- Bone Neoplasms
(metabolism, secondary)
- Breast Neoplasms
(metabolism, pathology)
- Cadherins
(biosynthesis)
- Female
- Humans
- Immunohistochemistry
|