Recycling of HER-ErbB Receptors: Rescue From Apoptosis and Targets for Immunotherapy

Abstract

Signals to multiply, migrate and outgrow blood vessels are mediated by growth factors of the EGF/neuregulin family. Concentrating on the membrane receptors for EGF and neuregulins, namely tyrosine kinases of the ErbB/HER family, our first task is to resolve mechanisms that normally restrain ErbB receptors. These efforts have led to the identification of a regulatory loop that allows collaboration between ErbB receptors and c-Src, a major oncoprotein of breast cancers. According to our findings, c-Src phopshorylates c-Cb1, a major restrainer of ErbB signaling, and leads to its proteasomal destruction. Consequently, tumor cells overexpressing c-Src or active Src mutants are unable to down-regulate ErbB proteins. Our Task 2 relates to a putative particle that modulates recycling of ErbBs. We report on the function of two components, Hgs and STAM, and their regulation by an ubiquitin ligase called Need4.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2002
Accession Number
ADA408134

Entities

People

  • Yosef Yarden

Organizations

  • Weizmann Institute of Science

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Albumins
  • Amino Acids
  • Biomedical And Dental Materials
  • Breast Cancer
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Confocal Microscopy
  • Growth Factors
  • Health Services
  • Molecules
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Polymer Chemistry
  • Proteins

Fields of Study

  • Biology

Readers

  • Breast cancer cell signaling and growth regulation.
  • Oncology

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech