European Journal of Nuclear Medicine and Molecular Imaging

, Volume 33, Issue 10, pp 1162–1170

In vitro and in vivo targeting of different folate receptor-positive cancer cell lines with a novel 99mTc-radiofolate tracer

  • Cristina Müller
  • P. August Schubiger
  • Roger Schibli
Original article

DOI: 10.1007/s00259-006-0118-2

Cite this article as:
Müller, C., Schubiger, P.A. & Schibli, R. Eur J Nucl Med Mol Imaging (2006) 33: 1162. doi:10.1007/s00259-006-0118-2

Abstract

Purpose

For the assessment of folate-based radiopharmaceuticals, human nasopharyngeal KB carcinoma cells are traditionally used although nasopharyngeal cancer is rare. On the other hand, the folate receptor (FR) is frequently overexpressed on diverse cancer types, the highest frequency (>90%) being on ovarian carcinomas. The goal of our study was the in vitro and in vivo assessment of different FR-positive human carcinoma cells. In addition, a murine sarcoma cell line was assessed as a pre-clinical alternative to human xenograft models.

Methods

FR-positive human nasopharyngeal, cervical, ovarian and colorectal cancer cell lines and the transgenic mouse sarcoma (24JK-FBP) cell line were targeted with a novel 99mTc-tricarbonyl folate derivative 2. Comparative in vitro cell binding studies were carried out under standardised folate-deficient conditions. In vivo studies were performed in nude mice and C6 black mice.

Results

The in vitro cell experiments revealed only FR-specific binding (unspecific <0.02%), ranging from 3.5% to 52% of complex 2 owing to variable levels of FR expression of the cell lines. In vivo tumour uptake of radiotracer 2 varied less than in vitro. It ranged from 0.66±0.17% ID/g (LoVo) through 1.16±0.64% ID/g (IGROV-1) and 1.55±0.43% ID/g (24JK-FBP) to 2.33±0.36% ID/g (KB) 4 h p.i.

Conclusion

These pre-clinical studies indicate that in vitro data obtained in FR-positive cancer cells do not necessarily correspond with or predict in vivo radiofolate uptake in corresponding (xeno)grafts. In addition, the murine 24JK-FBP cell line proved to be a valuable pre-clinical alternative to human tumour models.

Keywords

FolatesTumour targetingPre-clinical studiesDiagnostic potential

Copyright information

© Springer-Verlag 2006

Authors and Affiliations

  • Cristina Müller
    • 1
  • P. August Schubiger
    • 1
    • 2
  • Roger Schibli
    • 1
    • 2
  1. 1.Center for Radiopharmaceutical Science ETH-PSI-USZPaul Scherrer InstituteVilligen-PSISwitzerland
  2. 2.Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, ETH ZurichZurichSwitzerland