Identification of Druggable Proteins Regulating Receptor Recycling in Breast Cancer Cells

Abstract

Several recycling regulatory proteins are overexpressed in breast cancer patients and promote the progression of breast cancer. Increased receptor recycling leads to elevated receptors on the plasma membrane, thereby augments signaling cascades important in cancer progression and drives tumor aggressiveness. Inhibition of the altered recycling pathway in breast cancer cells would thus dampen oncogenic signaling and increase the efficacy of therapy. To screen druggable proteins regulating receptor recycling, we proposed to monitor EGFR trafficking using a newly developed AP-tag system. We found that while the AP-tag labeling worked for receptor endocytosis studies as described in the original literatures, it could not efficiently label the recycled EGFR. Therefore, this technique is not suitable for studying EGFR recycling as originally proposed.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2012
Accession Number
ADA568808

Entities

People

  • Guangwei Du

Organizations

  • University of Texas Health Science Center at Houston

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Amino Acids
  • Anatomy
  • Biomedical Research
  • Breast Cancer
  • Cell Line
  • Cell Membrane
  • Cell Physiological Processes
  • Cells
  • Cellular Structures
  • Department Of Defense
  • Identification
  • Inhibition
  • Literature
  • Membranes
  • Neoplasms
  • Proteins

Fields of Study

  • Biology

Readers

  • Environmental Engineering.
  • Oncology
  • Prostate Cancer Biology.