Restoration of Wild-Type Activity to Mutant p53 in Prostate Cancer: A Novel Therapeutic Approach

Abstract

A summary is presented of research performed during three years of a project to determine feasibility of approaches to restore wild-type transcriptional activity on mutant p53 proteins found in human prostate tumors. p53 mutant proteins that are specifically relevant to prostate cancer were examined to determine whether they are suitable targets for such an approach. Three specific aims were pursued. The first was characterizing the interaction of p53 with two distinct classes of its response elements. The second aim was determining the role of mutant p53 proteins in prostate cancer cell proliferation. The final aim was to explore approaches to restore wild-type function to mutant p53 proteins found in prostate cancer. The long-term goals of this research were to identify small molecular weight compounds that have the novel activity of restoring wild-type function to prostate cancer-derived mutant p53 proteins. As such, this represented a preclinical development of highly targeted therapy with the hope of establishing highly effective and tumor-specific treatments of human prostate cancer.

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Document Details

Document Type
Technical Report
Publication Date
Jan 01, 2008
Accession Number
ADA483167

Entities

People

  • James J. Manfredi

Organizations

  • Icahn School of Medicine at Mount Sinai

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Antibodies
  • Apoptosis
  • Biomedical Research
  • Cancer
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemotherapeutic Agents
  • Department Of Defense
  • Diseases And Disorders
  • Gene Expression
  • Mutant Proteins
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Proteins

Fields of Study

  • Biology

Readers

  • Oncology
  • Prostate Cancer Biology.