Development of a stereological method to measure levels of fluoropyrimidine metabolizing enzymes in tumor sections using laser scanning cytometry

Authors

  • Attila Megyeri,

    1. Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan
    Current affiliation:
    1. Department of Pharmacology, University of Debrecen School of Medicine, H-4012 Debrecen, Hungary
    Search for more papers by this author
  • Zsolt Bacsó,

    1. Department of Biophysics and Cell Biology, University of Debrecen School of Medicine, Debrecen, Hungary
    Search for more papers by this author
  • Anthony Shields,

    1. Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan
    Search for more papers by this author
  • James F. Eliason

    Corresponding author
    1. Barbara Ann Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan
    • Asterand, Inc., Tech One Suite 501, 440 Burroughs, Detroit, MI 48202
    Search for more papers by this author

Abstract

Background

The enzymes thymidine phosphorylase (TP) and dihydropyrimidine dehydrogenase (DPD) influence the activities of fluoropyrimidine anticancer drugs. The sensitivity of cancer cells to capecitabine, which is an oral, tumor-selective pre-prodrug of 5-fluorouracil may correlate better to the TP/DPD ratio than to levels of either enzyme alone. Our goal was to develop a quantitative immunofluorescent method for estimating the levels of TP, DPD, and their ratio in archival tumor sections.

Methods

Mouse anti-TP and rat anti-DPD monoclonal antibodies were used for parallel indirect immunofluorescent staining. The fluorescence was measured using a laser scanning cytometer (LSC; CompuCyte, Cambridge, MA) in single cells and in sections prepared from cell lines and a human tumor. The phantom contouring feature of the LSC provided a stereologic approach for collecting the fluorescence intensity data from sections.

Results

The relative fluorescence intensities measured in single cells or in sections of the cell lines, using single or double labeling, were similar, supporting the suitability of phantom contouring and two-color staining. Sections of the T-24 and ZR-75-1 cell lines placed on the same slide as the tumor section were used as internal standards for fluorescence measurements. The TP/DPD ratios measured in three cell lines correlated well with the cytotoxicity of 5′-deoxy-5-fluorouridine measured in vitro, indicating that the measurements are related to the biological activity of the drug.

Conclusions

Plotting the data as contour maps of the topologic distribution of fluorescence intensities in tumor sections allows subsequent histopathologic examination, which may reveal features of the tumors leading to high or low ratios of these enzymes. In addition, this method can be used for any drug target/metabolic system where the key components are known and suitable antibodies are available. © 2005 Wiley-Liss, Inc.

Ancillary