Targeting EGFR-positive cancer cells with cetuximab-ZZ-PE38: Results of in vitro and in vivo studies

Itay Barnea, Rahamim Ben-Yosef, Victoria Karaush, Itai Benhar, Akiva Vexler

Research output: Contribution to journalArticlepeer-review

Abstract

Background Arming antibody with toxins is a new approach in cancer therapy. We evaluated the efficacy of cetuximab-ZZ-PE38 immunocomplex in killing cancer cells in vitro and inhibiting tumor growth in nude mice. Methods Several cancer cell lines and human foreskin fibroblasts were tested for epidermal growth factor receptor (EGFR) expression and cetuximab binding using Western blot assay, enzyme-linked immunosorbent assay (ELISA), and flow cytometry. Cell survival in vitro was estimated by XTT assay. Tumor size was measured twice a week. Results Cetuximab-ZZ-PE38 immunocomplex was significantly more effective in killing head and neck cancer cells than nonspecific IgG-ZZ-PE38 complex or free ZZ-PE38, whereas normal cells were not affected. Tumor treatment with immunocomplex resulted in tumor shrinkage. The immunocomplex was safe to mice at a therapeutic dosage of 0.25 mg/mL, whereas the dosage of 0.50 mg/mL induced liver toxicity. Conclusions Cetuximab-ZZ-PE38 immunocomplex is a highly effective agent in killing EGFR-positive cancer cells and in tumor shrinkage.

Original languageEnglish
Pages (from-to)1171-1177
Number of pages7
JournalHead and Neck
Volume35
Issue number8
DOIs
StatePublished - Aug 2013

Keywords

  • EGFR
  • Pseudomonas exotoxin A
  • cetuximab
  • head and neck cancer
  • prostate cancer

All Science Journal Classification (ASJC) codes

  • Otorhinolaryngology

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