Role of Mesenchymal-Derived Stem Cells in Stimulating Dormant Tumor Cells to Proliferate and Form Clinical Metastases

Abstract

Tumor metastasis is a complex and often fatal complication of many different cancers. One of the biggest challenges to treatment is that prior to diagnosis or during treatment tumor cells can disseminate and remain dormant in distant tissue sites. These cells can become proliferative and lead to metastatic disease late after completion of therapy. The biology of this outbreak of dormant tumor cells that leads to relapsed metastatic disease is the major focus of this grant. Using a fibrosis model of tumor dormancy we have determined the break in dormancy is dependent on collagen and other fibrotic extracellular matrix components for the induction of a proliferative state in these dormant D2.0R breast cancer cell lines. Performing gene expression array on these dormant D2.0R cells exposed to collagen to induce a break from dormancy compared to dormant D2.0R cells revealed a set of genes that overlap with published dormancy gene sets. We also have performed immunophenotyping of the microenvironment of proliferating D2.0R cells in the fibrosis model of tumor dormancy and have identified an expansion of mesenchymal stem cells coincident with this metastatic outgrowth. We are now performing studies to analyze the key chemokine/cytokines released from the tumor cells transitioning from a dormant to proliferative state that may recruit these mesenchymal cells. We then plan to delve deeper into the crosstalk between these mesenchymal cell populations and the tumor cells to delineate the molecular pathways, which inform this complex biology. We plan to use both our in vivo and in vitro models with conditional gene deletion in the specific cell populations to determine the functional role of each key molecular component in the break from tumor dormancy. We anticipate these findings can identify potential therapeutic approaches to inhibit metastatic progression.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2015
Accession Number
ADA622388

Entities

People

  • Jeffrey Green

Organizations

  • Geneva Foundation

Tags

DTIC Thesaurus Topics

  • Bone Marrow
  • Bone Marrow Cells
  • Breast Cancer
  • Cancer
  • Cells
  • Cellular Structures
  • Cytokines
  • Diseases And Disorders
  • Fibrosis
  • Gene Expression
  • Medical Personnel
  • Membranes
  • Metastasis
  • Neoplasms
  • Proteins
  • Stem Cells
  • Stromal Cells

Fields of Study

  • Biology
  • Medicine

Readers

  • Data Mining and Knowledge Discovery.
  • Immunology and Pathology
  • Molecular Biology and Genetics

Technology Areas

  • Biotechnology