EGF receptor family targets for cancer therapeutics /

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Bibliographic Details
Other Authors: Burgess, Antony, 1946- (Speaker)
Format: Electronic Video
Language:English
Published: London : Henry Stewart Talks, 2007.
Series:Henry Stewart talks. Biomedical & life sciences collection. Signal transduction via protein tyrosine kinase receptors : structures, function, regulation, mechanisms and role in disease.
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Online Access:https://hstalks.com/bs/456/
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Table of Contents:
  • Contents: The association of the Epidermal Growth Factor Receptor (EGFR) with the tumorigenic state
  • The four related members of the EGFR family (EGFR, erbB2, erbB3 and erbB4)
  • Signaling of the activated receptors as either homo- or heteromeric oligomers
  • Activation of the EGFR by excess ligand stimulation, receptor over-expression and/or mutation in many carcinomas
  • Utility of antibodies and receptor kinase inhibitors which interfere with signaling from the EGFR family as agents in cancer therapy
  • The three-dimensional structures for the extracellular domains of EGFR, erbB2, erbB3 and erbB4 and the discovery that EGFR, erbB3 and erbB4 undergo major conformational transitions when interacting with their ligands
  • Development of antibodies (mab806) which reduce tumor formation from cells expressing either truncated D2-7 EGFR or over-expressed EGFR by binding to the receptor in a region normally masked by the dimerization of the EGFR extracellular domain
  • Use of EGFR antagonists or inhibitors to increase tumor killing by cytotoxic anti-cancer drugs and/or radiation
  • Improvement of tumor killing by combining EGFR antagonists and EGFR kinase inhibitors.