Analysis of the Regulation of Expression of Transforming Growth Factor-Beta in Human Breast Cancer Cells.

Abstract

This grant entails two objectives. The first objective derived from prior work which identified TGF-beta1 as an important cytokine in breast cancer. The specific goal of this objective was to identify the molecular mechanism of overexpression of TGF-beta1. We have analyzed paired normal and tumor specimens from patients and have determined that this genetic locus is not amplified in a significant proportion of patients. In other work we have recently obtained data which refutes the suggestion that overexpression of TGF-beta1 is associated with poor patient outcome. The second objective of the grant was to identify the molecular determinants of promoter usage for TGF-beta3 in breast cancer cell lines. In the past year we have focussed on examination of the methylation pattern at CpG sites in the vicinity of the two TGF-beta3 promoters. We have observed that whereas CpG sites closest to the breast cancer-specific downstream promoter are methylated in non breast cancer cells, they are unmethylated in breast cancer cells.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1997
Accession Number
ADA341594

Entities

People

  • Bradley A. Arrick

Organizations

  • Dartmouth College

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Cell Line
  • Cells
  • Chemical Reactions
  • Chemistry
  • Diseases And Disorders
  • Estrogens
  • Growth Factors
  • Materials
  • Methylation
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Phosphodiesterases
  • Polymerase Chain Reaction
  • Proteins
  • Regulations

Fields of Study

  • Medicine

Readers

  • Breast cancer cell signaling and growth regulation.
  • Oncology and Biomarker-Based Cancer Detection.
  • Theoretical Analysis.

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech