Regulation of the Prostate Cancer Tumor Microenvironment

Abstract

Toll-like receptors (TLRs) are key signaling molecules that regulate innate and adaptive immune responses to the presence of pathogens. The role of TLRs in cancer is unclear. During our first year of this training proposal, we are expanding transgenic and transgenic crosses to various TLR signaling molecules for Specific Aims 1 and 2. We have generated TRAMP Tg+/- x MyD88-/- mice. Initial results reveal that de novo prostate cancers in absence of MyD88 are larger with higher grade adenocarcinomas than wild-type controls. Analysis of tumor infiltrating cells reveals increased infiltrating macrophage lineage in the absence of MyD88. We are in the process of understanding the activation of signaling pathways, local and systemic cytokine levels, and other infiltrating cell types that may modulate the differences in tumor development. We are also isolating TRAMP Tg/- cell lines deficient in MyD88 to ascertain the role of MyD88 in the intrinsic growth of TRAMP prostate cancer cells.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 2012
Accession Number
ADA560887

Entities

People

  • Arnold I. Chin

Organizations

  • University of California, Los Angeles

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Cancer
  • Cells
  • Diseases And Disorders
  • Immunity
  • Lymphocytes
  • Mononuclear Phagocyte System
  • Neoplasms
  • Pathogenic Bacteria
  • Pattern Recognition
  • Prostate
  • Prostate Cancer
  • Proteins
  • Regulations
  • T Lymphocytes

Fields of Study

  • Medicine

Readers

  • Immunology
  • Oncology (Cancer Research).