RNA-Binding Proteins as Novel Oncoproteins and Tumor Suppressors in Breast Cancer

Abstract

Posttranscriptional control of gene expression is particularly important for oncoproteins and cell cycle proteins because their sustained synthesis favors cell growth rather than differentiation, a hallmark of the neoplastic phenotype. Control is exerted via the opposing actions of the RNA-binding proteins AUF1 and HuR. AUF1 triggers degradation of mRNA subsets while HuR promotes mRNA stabilization. Phase I of this work is to examine the effects of AUF1 and HuR expression levels on global gene expression in human breast carcinoma cells. Phase II is to assess roles of AUF1 and HuR in cellular proliferation and tumorigenesis in vivo. During this funding period, we discovered that AUF1 knockdown accelerates breast cancer cell proliferation and may convert cells to a highly metastatic state. Moreover, AUF1 knockdown elevates expression of the c-myc proto-oncogene, consistent with accelerated proliferation. mRNP immunoprecipitation and RT-PCR revealed that AUF1 binds c-myc mRNA in cells. Our results reveal a new paradigm for tumor metastasis and invasion in breast cancer.

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Document Details

Document Type
Technical Report
Publication Date
May 01, 2006
Accession Number
ADA456197

Entities

People

  • Gary Brewer

Organizations

  • University of Medicine and Dentistry of New Jersey

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Cancer
  • Carrier Proteins
  • Cell Cycle Proteins
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Cultured Cells
  • Dna Microarrays
  • Gene Expression
  • Genes
  • Genetics
  • Medical Personnel
  • Mrna
  • Neoplasms
  • Proteins
  • Tumor Cell Line

Fields of Study

  • Biology

Readers

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