Regulation and Mechanism of Action of the C-MYC Proto-Oncogene in Human Breast Cancer.

Abstract

The biological relevance of the c-Myc/YY1 association has been established by demonstrating that the two proteins associate in vivo and showing that the amount of YY1 associated with c-Myc varies when c-Myc levels change. We have also shown that association with c-Myc does not inhibit the ability of YY1 to bind DNA, but appears to alter its ability to associate with basal transcription proteins TBP and TF-IIB. Steady-state c-myc RNA in MCF-7 cells was shown to increase approximately 1OX in response to estrogen. We expect that at least part this effect depends on transcription because we have identified two estrogen-dependent DNase I hypersensitive sites in the c-myc gene. One of these maps to a region containing NF-kB and C/EBP sites. We are exploring how these proteins may mediate a response to estrogen. Finally, we have shown that PRDIBFI/Blimp-1 is a repressor of c-myc transcription. We are exploring its mechanism of action and determining how overexpression of the gene may alter the growth phenotype of various breast tumor cell lines.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1995
Accession Number
ADA303163

Entities

People

  • Kathryn Calame

Organizations

  • Columbia University

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Biomedical And Dental Materials
  • Blood
  • Breast Cancer
  • Cell Line
  • Cells
  • Chemical Compounds
  • Chemical Synthesis
  • Chemistry
  • Estrogens
  • Immune Serums
  • Neoplasms
  • Polymer Chemistry
  • Polymeric Films
  • Proteins
  • Steady State
  • Tumor Cell Line

Fields of Study

  • Biology

Readers

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