A fully human anti-Ep-CAM scFv-beta-glucuronidase fusion protein for selective chemotherapy with a glucuronide prodrug

M. De Graat, E. Boven, D. Oosterhoff, I. H. Van der Meulen-Muileman, G. A. Huls, W. R. Gerritsen, H. J. Haisma, H. M. Pinedo

Research output: Contribution to journalArticlepeer-review

31 Scopus citations


Monoclonal antibodies against tumour-associated antigens could be useful to deliver enzymes selectively to the site of a tumour for activation of a non-toxic prodrug. A completely human fusion protein may be advantageous for repeated administration, as host immune responses may be avoided. We have constructed a fusion protein consisting of a human single chain Fv antibody, C28, against the epithelial cell adhesion molecule and the human enzyme β-glucuronidase. The sequences encoding C28 and human enzyme β-glucuronidase were joined by a sequence encoding a flexible linker, and were preceded by the IgGK signal sequence for secretion of the fusion protein, A CHO cell line was engineered to secrete C28-β-glucuronidase fusion protein. Antibody specificity and enzyme activity were retained in the secreted fusion protein that had an apparent molecular mass of 100 kDa under denaturing conditions. The fusion protein was able to convert a non-toxic prodrug of doxorubicin, N-[4-doxorubicin-N-carbonyl(oxymethyl)phenyl]-O-β-glucuronyl carbamate to doxorubicin, resulting in cytotoxicity, A bystander effect was demonstrated, as doxorubicin was detected in all cells after N-E4-doxorubicin-N-carbonyl(oxymethyl)phenyl]-O-β-glucuronyl carbamate administration when only 10% of the cells expressed the fusion protein. This is the first fully human and functional fusion protein consisting of an scFv against epithelial cell adhesion molecule and human enzyme β-glucuronidase for future use in turnout-specific activation of a non-toxic glucuronide prodrug,

Original languageEnglish (US)
Pages (from-to)811-818
Number of pages8
JournalBritish journal of cancer
Issue number5
StatePublished - 2002
Externally publishedYes


  • Anthracyclines
  • Cancer chemotherapy
  • Glucuronide
  • Human fusion protein
  • β-glucuronidase

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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