Secreted and tumour targeted human carboxylesterase for activation of irinotecan

D. Oosterhoff, H. M. Pinedo, I. H. Van der Meulen, M. De Graaf, T. Sone, F. Kruyt, V. W. Van Beusechem, H. J. Haisma, W. R. Gerritsen

Research output: Contribution to journalArticlepeer-review

30 Scopus citations


Irinotecan (CPT-11) is an anticancer agent for the treatment of colon cancer, CPT-11 can be considered as a prodrug, since it needs to be activated into the toxic drug SN-38 by the enzyme carboxylesterase. An approach to achieve tumour specific activation of CPT-11 is to transduce the cDNA encoding carboxylesterase into tumour cells. A secreted form of carboxylesterase may diffuse through a tumour mass and may activate CPT-11 extracellularly. This could enhance the antitumour efficacy by exerting a bystander effect on untransduced cells. In addition a secreted tumour-targeted form of carboxylesterase should prevent leakage of the enzyme from the site of the tumour into the circulation. We have constructed a secreted form of human liver carboxylesterase-2 by deletion of the cellular retention signal and by cloning the cDNA downstream of an Ig kappa leader sequence. The protein was secreted by transfected cells and showed both enzyme activity and efficient CPT-11 activation. To obtain a secreted, tumour-targeted form of carboxylesterase-2 the cDNA encoding the human scFv antibody C28 directed against the epithelial cell adhesion molecule EpCAM, was inserted between the leader sequence and carboxylesterase-2. This fusion protein showed CPT-11 activation and specific binding to EpCAM expressing cells. Importantly, in combination with CPT-11 both recombinant carboxylesterase proteins exerted strong antiproliferative effects on human colon cancer cells. They are, therefore, promising new tools for gene directed enzyme prodrug therapy approaches for the treatment of colon carcinoma with CPT-11.

Original languageEnglish (US)
Pages (from-to)659-664
Number of pages6
JournalBritish journal of cancer
Issue number6
StatePublished - 2002
Externally publishedYes


  • CPT-11
  • Cancen
  • Carboxylesterase
  • Chemotherapy
  • Prodrug
  • SN-38

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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