Role of CEACAM1, ECM, and Mesenchymal Stem Cells in an Orthotopic Model of Human Breast Cancer

Author:

Samineni Sridhar12,Glackin Carlotta3,Shively John E.2

Affiliation:

1. Irell & Manella City of Hope Graduate School of Biological Sciences, Duarte, CA 91010, USA

2. Department of Immunology, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA

3. Department of Neurosciences, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA

Abstract

Carcinoembryonic antigen-related cell adhesion molecule-1 (CEACAM1) is a morphogen in anin vitromodel for lumen formation and plays a similar role in breast epithelial cells implanted in humanized mammary fat pads in NOD-SCID mice. Although extra cellular matrix alone is sufficient to stimulate lumen formation in CEACAM1 transfected MCF-7 cells grown in 3D culture, there is an additional requirement for stromal or mesenchymal cells (MSCs) for these cells to form xenografts with glandular structures in an orthotopic site. We demonstrate that optimalin vitroconditions include both Matrigel and MSCs and that the inclusion of collagen I inhibits xenograft differentiation. Additionally, there is no need to remove the nascent murine mammary gland. The previously observed difference in gland development between the long and short cytoplasmic domain isoforms of CEACAM1 is no longer observed in pregnant NOD/SCID mice suggesting that stimulation of the mammary fat pad by pregnancy critically affects xenograft differentiation.

Funder

National Institutes of Health

Publisher

Hindawi Limited

Subject

Cancer Research,Pharmacology (medical),Oncology

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