Regulation of AR and (Beta)-Catenin Signaling by Pin 1 in Prostate Cancer

Abstract

This mid-term report is a summary of the work accomplished during the past research year. The majority of this work was included in the attached Manuscript. Additional data were also included. Together our data support a positive role of Pin1 in PCa progression. We demonstrated that Pin1 can enhance beta-catenin nuclear localization, TCF/beta-catenin dependent promoter activity, and c-Myc and Cyclin D1 expression, while disrupt AR-mediated suppression of TCF/beta-catenin signaling. We also determined that Pin1 can reduce AR transcriptional activity and PSA expression, although the importance and the molecular basis for this Pin1 action are still not clear.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 2005
Accession Number
ADA446378

Entities

People

  • Shaoyong Chen

Organizations

  • Beth Israel Deaconess Medical Center

Tags

DTIC Thesaurus Topics

  • Androgen Receptors
  • Blood
  • Cancer
  • Cell Line
  • Cells
  • Chemistry
  • Colon Cancer
  • Department Of Defense
  • Diseases And Disorders
  • Epithelium
  • Health Services
  • Neoplasms
  • Prostate
  • Prostate Cancer
  • Proteins
  • Regulations
  • Tissues

Readers

  • Molecular Biology and Genetics
  • Prostate Cancer Biology.
  • Systems Analysis and Design