Mechanisms of Abnormal Cell-Extracellular Matrix Interactions in Human Breast Cancer.

Abstract

By a three-dimensional reconstituted basement membrane (EHS matrix) assay, we have previously shown that breast morphogenesis is regulated by cell-extracellular matrix (ECM) interactions and these contacts are impaired in malignancy. A series of studies were conducted to investigate the significance of cell/ECM interactions in tumorigenesis. ECM influences expression of lactoferrin, a differentiation marker, either by altering cell-cell interactions or by providing mechanochemical signals that regulate cell shape. Emphasis on the importance of intact beta-1-integrin signaling was indicated by function blocking studies. Phenotypically normal HMT-3522 cells failed to grow or differentiate and underwent apoptosis in the presence of beta-1 integrin blocking antibodies. In contrast a number of tumorigenic cell lines demonstrated refractoriness to these effects indicating they have circumvented this regulatory pathway. Finally the importance of cell/ECM interactions in the maintenance of the differentiated phenotype was underscored by examining the effects of overexpression of the putative tumor suppressor gene nm23-H1 in metastatic cell line MDA-MB- 435, where several aspects of normal breast morphogenesis was recapitulated. Further studies are presently underway to dissect other ECM components and their signaling pathways that are critical in breast cancer progression.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1995
Accession Number
ADA303616

Entities

People

  • Anthony R. Howlett
  • Mina Bissell

Organizations

  • University of California, Berkeley

Tags

DTIC Thesaurus Topics

  • Biological Sciences
  • Blood
  • Breast Cancer
  • Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cell Shape
  • Cells
  • Cellular Structures
  • Chemical Synthesis
  • Chemistry
  • Epithelial Cells
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Proteins
  • Three Dimensional

Fields of Study

  • Biology

Readers

  • Neuroscience
  • Oncology (Cancer Research).