Modulation of Anaplastic Lymphoma Kinase Upon Tumor-Stroma Interaction and Its Implications for Tumor Growth and Metastasis in Breast Cancer

Abstract

Induction of neovascularization is needed for a growing tumor as well as for its metastasis. Angiogenic and growth promoting factors like Pleiotrophin (PTN) act on endothelial and epithelial cells and on fibroblasts. We identified the receptor for PTN as anaplastic lymphoma kinase(ALK). In individual tissues the presence of ALK is elevated in tumor stroma (endothelium) while adjacent normal tissue lacked ALK. In cultured endothelial cells or human fibroblasts ALK is upregulated in response to supernatants from human breast cancer cells. Our hypothesis is that ALK from stromal cells upregulated in response to factors from tumor cells, constitutes a marker and a potential therapeutic target in breast cancer. We investigated the specificity of ALK modulation in tumor stroma versus normal endothelium in response to growth factors and breast cancer cell lines supernatants. We underscored the importance of the ALKIPTN axis in migration and invasion and we blocked these effects with blocking antibodies. The completion of the study will translate in establishing ALK as a new target for the breast metastatic cancer therapy.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2005
Accession Number
ADA446352

Entities

People

  • Elly-gerald Stoica

Organizations

  • Georgetown University

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Antibodies
  • Blood
  • Blood Vessels
  • Breast Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Culture Media
  • Data Sets
  • Department Of Defense
  • Endothelial Cells
  • Endothelium
  • Fibroblasts
  • Growth Factors
  • Metastasis
  • Migration
  • Tissues

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Immunology
  • Molecular Biology and Genetics