The LCC15-MB human breast cancer cell line expresses osteopontin and exhibits an invasive and metastatic phenotype

Sung, V., Gilles, C., Murray, A., Clarke, R., Aaron, A.D., Azumi, N., & Thompson, E.W. (1998) The LCC15-MB human breast cancer cell line expresses osteopontin and exhibits an invasive and metastatic phenotype. Experimental Cell Research, 241(2), pp. 273-284.

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Abstract

We have characterized the LCC15-MB cell line which was recently derived from a breast carcinoma metastasis resected from the femur of a 29-year-old woman. LCC15-MB cells are vimentin (VIM) positive, exhibit a stellate morphology in routine cell culture, and form penetrating colonies when embedded in three-dimensional gels of Matrigel or fibrillar collagen. They show high levels of activity in the Boyden chamber chemomigration and chemoinvasion assays, and like other invasive human breast cancer (HBC) cell lines, LCC15-MB cells activate matrix-metalloproteinase-2 in response to treatment with concanavalin A. In addition, these cells are tumorigenic when implanted subcutaneously in nude mice and recolonize bone after arterial injection. Interestingly, both the primary lesion and the bone metastasis from which LCC15-MB were derived, as well as the resultant cell line, abundantly express the bone matrix protein osteopontin (OPN). OPN is also expressed by the highly metastatic MDA-MB-435 cells, but not other invasive or noninvasive HBC cell lines. Expression of OPN is retained in the subcutaneous xenograft and intraosseous metastases of LCC15-MB as detected by immunohistochemistry. Both VIM and OPN expression have been associated with breast cancer invasion and metastasis, and their expression by the LCC15-MB cell line is consistent with its derivation from a highly aggressive breast cancer. These cells provide a useful model for studying molecular mechanisms important for breast cancer metastasis to bone and, in particular, the implication(s) of OPN and VIM expression in this process.

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ID Code: 72176
Item Type: Journal Article
Refereed: Yes
Additional Information: Cited By (since 1996):44
Export Date: 6 May 2014
Source: Scopus
PubMed ID: 9637769
Additional URLs:
DOI: 10.1006/excr.1998.4029
ISSN: 0014-4827
Divisions: Current > QUT Faculties and Divisions > Faculty of Health
Deposited On: 28 May 2014 02:09
Last Modified: 28 May 2014 02:09

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