Molecular Effects of 13C/DIM in Prostate Cancer

Abstract

We have previously shown anti-proliferative and pro-apoptotic effects of 13C and DIM through the NF- B pathway in prostate cancer cells. To further explore the molecular mechanisms involved in the regulation of NF- B by I3C/DIM, we investigated the effects of B-DIM, a formulated DIM with greater bioavailability, on AR, Akt, and NF- B signaling in hormonesensitive LNCaP and hormone-insensitive C4-2B prostate cancer cells. We found that B-DIM significantly inhibited cell growth and induced apoptosis in both cell lines. By Akt transfection, RT-PCR, Western Blot analysis, and EMSA, we found that there could be a crosstalk between Akt, NF- B, and AR in cell signaling. Importantly, we found that B-DIM significantly inhibited Akt activation, NF- B DNA binding activity, and the expressions of AR and PSA, interrupting the crosstalk. Moreover, our confocal image study revealed that B-DIM inhibited AR nuclear translocation, leading to the down-regulation of AR target genes including PSA. These results suggest that B-DIM could inhibit cell growth and induce apoptosis partly through downregulation of AR, Akt and NF- B signaling. These results along with our previous findings suggest that 13C and DIM may be potent agents for the prevention and/or treatment of androgen sensitive and androgen-refractory prostate cancers.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2006
Accession Number
ADA455890

Entities

People

  • Fazlul H. Sarkar

Organizations

  • Wayne State University

Tags

DTIC Thesaurus Topics

  • Apoptosis
  • Cardiovascular Diseases
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Colon Cancer
  • Confocal Microscopy
  • Diseases And Disorders
  • Epithelial Cells
  • Gene Expression
  • Lymphocytes
  • Neoplasms
  • Prostate Cancer
  • Proteins
  • Vascular Diseases

Fields of Study

  • Biology
  • Chemistry

Readers

  • Breast cancer cell signaling and growth regulation.
  • Prostate Cancer Biology.