Abstract

The radiosensitivity of human tumour cell lines and cells cultured from xenografts or biopsy specimens was measured using the adhesive tumour cell culture system (ATCCS). For cell lines the derived surviving fractions at 2 Gy were in good agreement with values obtained by clonogenic assay. However, the assay tended to overestimate survival at higher radiation doses, and thus to give a false impression of radioresistance. When cells taken from xenografts or tumour biopsies were cultured there was no evidence for selective growth of tumour cells: fibroblast-like cells commonly grew. Immunohistochemical staining against the intermediate filament, vimentin, supported the mesenchymal origin of the fibroblast-like cells. In cultures of artificial mixtures of tumour cells and fibroblasts, low proportions of fibroblasts were not excluded by the assay and consequently modified the radiation response. The majority of cultures grown from bladder carcinoma biopsy specimens appeared fibroblast-like, although in some cases clearly distinguishable colonies of tumour cells were also grown. In such tumour types the reliable measurement of radiosensitivity in cells taken from biopsies will require further development of techniques that allow the selective growth of tumour cells.

Highlights

  • LLttdd.., Growth and radiosensitivity testing of human tumour cells using the adhesive tumour cell culture system

  • Using human tumour cell lines we found the derived dose-response to be in close agreement with that from a clonogenic assay the sensitivity at higher doses was underestimated

  • For our cell lines no significant increase in cloning efficiency (CFE) was observed using the cell adhesive matrix (CAM) coating compared to growth on tissue culture grade surfaces

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Summary

Introduction

LLttdd..,, Growth and radiosensitivity testing of human tumour cells using the adhesive tumour cell culture system. The goal of predictive testing is to quantify the in vitro radiosensitivity of tumour cells in a way that is predictive for the outcome after therapy. This might lead on to the selection of an altered treatment for radio-resistant tumours. A wide variety of assays to measure the radiosensitivity of tumour cells have been proposed (see Peters et al, 1986, for review) of which the adhesive tumour cell culture system (ATCCS) developed by Baker et al (1986) has been reported as a major advance (Baker et al, 1985, 1988a; Brock et al, 1985; Ajani et al, 1987; Malaise et al, 1987; Peters et al, 1987). Over the culture period the assay conditions are reported to enhance the growth of human tumour cells

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