Inflammation, Prostate Cancer and Negative Regulation of Androgen Receptor Expression

Abstract

My study involved two aspects of androgen receptor (AR) regulation-1) molecular mechanism underlying negative regulation of AR expression and activity, 2) microRNA-mediated regulation of prostate cancer cell proliferation. My data establish that the human AR level is negatively regulated by nuclear factor kB (NF-kB) following its activation by TNF-alpha-induced signaling. I have defined the regulatory region in the human AR promoter that responds to the TNF-alpha-controlled negative transcriptional regulation. I show that TNF-alpha-controlled inhibition of AR expression occurs in androgen-dependent LNCaP human prostate cancer cells, but not in the androgen-independent C4-2 human prostate cancer cells. I further show that TNF-alpha treatment caused recruitment of corepressor complexes on negative response region in LNCaP cells, but not in C4-2 cells. To search for the microRNA effect on prostate cancer, scanning of the cancer microRNA array shows that miR-454 is up regulated in androgen-independent C4-2 cells and overexpression of miR-454 enhanced prostate cancer cell proliferation. In addition, Slain1 is identified as a miR-454 target protein using bioinformatics approaches.

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Document Details

Document Type
Technical Report
Publication Date
May 01, 2009
Accession Number
ADA506652

Entities

People

  • Soyoung Ko

Organizations

  • University of Texas Health Science Center at San Antonio

Tags

DTIC Thesaurus Topics

  • Androgen Receptors
  • Anti-Bacterial Agents
  • Apoptosis
  • Biomedical Research
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Epithelial Cells
  • Health Services
  • Hormones
  • Inflammation
  • Inhibition
  • Neoplasms
  • Prostate Cancer
  • Proteins
  • Therapy
  • Thyroid Hormones

Fields of Study

  • Biology

Readers

  • Immunology and Pathology
  • Molecular Biology and Genetics
  • Prostate Cancer Biology.