Assessment of Nanobiotechnology-Targeted siRNA Designed to Inhibit NF-KappaB Classical and Alternative Signaling in Breast Tumor Macrophages

Abstract

Macrophages have been proposed as a potential target for manipulation of the microenvironment in breast cancer because they are potent effectors of the immune system. NF kappaB (NF B) signaling in macrophages contributes to their impact during breast tumorigenesis. Thus, macrophage targeted modulation of NF B has potential as a novel therapeutic approach for breast cancer. NF B signaling is mediated via two major pathways; the canonical/classical pathway and the alternative pathway. Our strategy is designed to develop a nanobiotechnology-based method to target siRNA designed to inhibit NF B classical and alternative signaling specifically to tumor associated macrophages to modulate the tumor microenvironment and to test the therapeutic potential of this approach. In this highly collaborative stufy, we have synthesized and characterized in vitro both mannosylated and untargeted nanoparticles. We have compared the efficiency of transfection of bone marrow derived.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2014
Accession Number
ADA613613

Entities

People

  • Fiona E. Yull

Organizations

  • Vanderbilt University

Tags

DTIC Thesaurus Topics

  • Biomedical And Dental Materials
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Health Services
  • Materials Science
  • Medical Personnel

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Immunology and Pathology
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech