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PMID: 10910049 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Reproductive state of rat mammary gland stroma modulates human breast cancer cell migration and invasion.

Cancer research ·Vol. 60 ·No. 13 ·2000-07-01 ·Pages 3414-8

Bemis LT, Schedin P

Abstract

It has been established that the invasive behavior of cancer cells can be regulated by alterations in their extracellular environment. We investigated whether extracellular matrix isolated from nulliparous and postlactating (involuting) rat mammary glands differentially modulated the metastatic behavior of human breast cancer cells. Using modified Boyden chamber and three-dimensional culture assays, nulliparous mammary matrix was found to suppress motility and invasion in highly metastatic MDA-MB-435 cells, whereas involution mammary matrix supported motility and invasion in highly metastatic MDA-MB-435 cells, but not in cells with low metastatic potential. Biochemical characterization of the matrices revealed intact fibronectin (FN) and low matrix metalloproteinase activity in nulliparous mammary matrix and fragmented FN and high matrix metalloproteinase activity in the matrix isolated from involuting glands. Purified intact FN was found to inhibit cell invasiveness, whereas FN fragments enhanced cell invasiveness in a matrix metalloproteinase-dependent manner. These data suggest that physiological changes that occur in the mammary extracellular matrix as a result of reproductive status alter the in vitro parameters of metastatic potential.

MeSH Terms
Animals Breast Neoplasms/pathology,physiopathology Cell Movement Cells, Cultured Coculture Techniques Female Fibronectins/physiology Humans Mammary Glands, Animal/cytology Matrix Metalloproteinases/metabolism Neoplasm Invasiveness Neoplasm Metastasis Rats Rats, Sprague-Dawley Stromal Cells/cytology,physiology Tumor Cells, Cultured
Chemicals
Fibronectins Matrix Metalloproteinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bemis L T
University of Colorado Health Sciences Center, Cancer Center, Medical Oncology, Denver, Colorado 80262, USA.
Schedin P
Article Info
Journal
Cancer research
Abbr.
Cancer Res
ISSN
0008-5472
Published
2000-07-01
Pages
3414-8
Language
English
Region
United States
NLM ID
2984705R
Subset
IM
Grants
NCI NIH HHS · R29 CA70915-01 · United States
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