Adipocyte Differentiation: Relationship to Breast Cancer

Abstract

We hypothesize that breast malignant epithelial cells interact with surrounding stroma to provide biochemical and structural support for tumor tissue. Specifically, malignant epithelial cells block the differentiation of surrounding adipose fibroblasts through cytokines. Additional epithelial factors strikingly induce aromatase expression in these undifferentiated fibroblasts via switching aromatase gene promoter use from the physiologically used promoter 1.4 to aberrantly activated promoter II. During this entire grant period, we have accomplished all specific aims. First, we showed that factors secreted by malignant epithelium inhibit diffemtiation of adipose fibroblasts to mature adipocytes. These epithelial factors were identified as TNF and IL- 11. TNF and IL-il suppress essential adipogenic transcription factors C/ElBPa and PPAR7 in undifferentiated adipose fibroblasts. Since aromatase expression resides only in undifferentiated fibroblasts but not in mature adipocytes, inhibition of differentiation serves to increase aromatase-expressing cells around malignant epithelial cells. As a second hit, malignant epithelium secretes additional factors other than TNF or IL-il to upregulate aromatase expression in adipose fibroblasts. We demonstrated that the transcription factor C/EBP(3 mediates this malignant epithelial cell effect on adipose fibroblasts. C/EBP(3 binds to promoter II to activate this pathologic promoter in fibroblasts in tumor tissue. The end result is aromatase overexpression and increased local formation of estrogen in breast cancer.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2002
Accession Number
ADA405263

Entities

People

  • Berdar E. Bulun

Organizations

  • University of Illinois at Chicago

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Breast Cancer
  • Carrier Proteins
  • Cell Line
  • Cells
  • Chemistry
  • Culture Media
  • Culture Techniques
  • Cytokines
  • Epithelial Cells
  • Fat Cells
  • Fibroblasts
  • Inhibition
  • Neoplasms
  • Proteins
  • Tissues
  • Transcription Factors

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Immunology and Pathology
  • Oncology (Cancer Research).