Retinoids and Histone Deacetylase Inhibitors in the Treatment of Prostate Cancer

Abstract

Retinoids, derivatives of vitamin A (retinol), are required for the appropriate differentiation of normal human prostate epithelial cells. Human prostate cancer cells contain much lower levels of vitamin A and its metabolites that normal cells. We hypothesize that aberrant metabolism of vitamin A and dysregulation of gene expression in prostate tumor cells are related to the abnormal growth properties of the tumor cells. A rationale for using retinoids in prostate cancer chemotherapy is further supported by the effectiveness of ATRA (all-trans Retinoic Acid), a vitamin A metabolite, in the treatment of acute promyelocytic leukemia (APL). We hypothesize that the efficacy of retinoic acid can be enhanced if it is administered in combination with low doses of selective, potent histone deacetylase inhibitors such as trichostatin A (TSA or valproic acid). The goals of this idea grant are to use mouse xenograft models to ascertain the effectiveness of various retinoids plus his tone deacetylase inhibitors in inhibiting the growth and inducing the differentiation of the human prostate cancer lines LNCaP and PC-3. A second goal of the project is to understand at the molecular level the mechanisms by which the combination of retinoids acid and his tone deacetylase inhibitors result in human prostate tumor cell growth inhibition. In the past year, we have begun the xenograft experiments, employing 13-cis RA and valproic acid. We have also continued to perform a variety of biochemical and molecular biological assays on human prostate cancer cells treated with various combinations of the aforementioned drugs in order to gain more insight into the molecular mechanisms involved in cell growth inhibition. The studies that we have performed, and the studies proposed in the next period of this Idea Development grant should provide a much clearer rationale for new clinical treatments for prostate cancer in humans.

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Document Details

Document Type
Technical Report
Publication Date
Dec 01, 2003
Accession Number
ADA421967

Entities

People

  • Lorraine J. Gudas

Organizations

  • Cornell University

Tags

DTIC Thesaurus Topics

  • Acids
  • Anticonvulsants
  • Biomedical Research
  • Cancer
  • Cell Line
  • Cell Physiological Processes
  • Chemotherapy
  • Enzyme Inhibitors
  • Gene Expression
  • Inhibition
  • Inhibitors
  • Leukemia
  • Neoplasms
  • Prostate Cancer
  • Retinoic Acids
  • Therapy
  • Xenografts

Fields of Study

  • Biology
  • Medicine

Readers

  • Molecular Biology and Genetics
  • Oncology (Cancer Research).
  • Prostate Cancer Biology.