Preclinical Studies with Human Tumour Xenografts Using Rat Monoclonal Antibodies Directed Against the Epidermal Growth Factor Receptor

  • S. A. Eccles
  • H. Modjtahedi
  • W. Court
  • J. Titley
  • G. Box
  • C. Dean
Conference paper
Part of the Ernst Schering Research Foundation Workshop book series (SCHERING FOUND, volume 19)

Abstract

There is abundant evidence to suggest that over-expression of growth factor receptors and/or autocrine production of one or more ligands may provide tumour cells with significant advantages in growth and dissemination. One clinically important group is that of the c-erbB family of type 1 receptor tyrosine kinases exemplified by epidermal growth factor receptor (EGFR; reviewed by Harris et al. 1992; Khazaie et al. 1993; Modjtahedi and Dean 1994; Baselga and Mendelsohn 1994; Eccles et al. 1995). The cell surface location of these molecules renders them attractive targets for a variety of immunotherapeutic strategies, some of which are showing promise in preclinical and early clinical trials.

Keywords

Toxicity Carbohydrate Tyrosine Adenocarcinoma Oncol 

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Copyright information

© Springer-Verlag Berlin Heidelberg 1997

Authors and Affiliations

  • S. A. Eccles
  • H. Modjtahedi
  • W. Court
  • J. Titley
  • G. Box
  • C. Dean

There are no affiliations available

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