Malignant Mammary Cells Acquire Independence from Extracellular Context for Regulation of Estrogen Receptor α

Virginia Novaro, Derek C. Radisky, Nancy E. Ramos Castro, Alessandro Weisz, Mina J. Bissell

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


Interactions between luminal epithelial cells and their surrounding microenvironment govern the normal development and function of the mammary gland. Alterations of these interactions can induce abnormal intracellular signaling pathways that affect the development and progression of breast tumors. One critical component of mammary gland development, as well as breast cancer progression, is the expression of estrogen receptors. In a previous study using cultured nonmalignant mammary epithelial cells, we found that the basement membrane molecules, laminin-1 and collagen-IV, were involved in maintenance of estrogen receptor (ER) α expression, and that this response could be interfered with by disrupting cell-extracellular matrix adhesion. Here we use phenotypically normal mammary epithelial SCp2 cells to dissect the promoter region of the ERα that is involved in the selective response to basement membrane. We also analyze the alteration of this response in SCg6 cells, a malignant cell line that shares a common lineage with the SCp2 cells, to provide insight into the relative overexpression of ERα and the unresponsiveness to basement membrane regulation found in those malignant cells. Evidence is presented to show the relevance of the cross-talk between different signaling pathways in the constitution of a functional tissue organization and how this integration may be disrupted in the malignant phenotype.

Original languageEnglish (US)
Pages (from-to)402s-409s
JournalClinical Cancer Research
Issue number1
StatePublished - Jan 28 2004

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


Dive into the research topics of 'Malignant Mammary Cells Acquire Independence from Extracellular Context for Regulation of Estrogen Receptor α'. Together they form a unique fingerprint.

Cite this