1. ¹School of Biomedical Sciences, University of Ulster, Newtownabbey, BT37 OQB, Northern Ireland
2. ²Radiation Science Centre, Dublin Institute of Technology, Dublin

Correspondence: Professor DG Hirst, E-mail: DG.Hirst@ulst.ac.uk

Received 16 April 2003; Revised 9 September 2003; Accepted 16 September 2003.

Abstract

The intrinsic radiation sensitivity of normal and tumour tissue is a major determinant of the outcome of radiotherapy. There is currently no established test that can be used routinely to measure the radiosensitivity of the cells in an individual patient's cancer in a manner that can inform treatment planning. The purpose of this study was to evaluate, in four human colorectal adenocarcinoma cell lines, two possible end points as surrogate markers of radiation response – apoptosis and induction of DNA single-strand breaks – and to compare the results with those of a conventional clonogenic assay. Cell lines (SW707 SW480, SW48 and HT29) known to differ in radiosensitivity were exposed to single doses of X-rays ranging from 0.5 to 5 Gy and cell survival was measured using the clonogenic assay. Apoptosis was determined on the basis of morphology under fluorescent microscopy and DNA damage/repair was measured, as tail moment, using an adaptation of the alkaline comet assay. The relationship between surviving fraction at 2 Gy (SF₂) and the percentage of apoptotic cells 24 h after the same dose was complex, but apoptosis accurately predicted the order of radiosensitivities as measured by SF₂. Initial damage measured after 2 Gy using the alkaline comet assay gave a close correlation with SF₂ (r²=0.95), whereas there was no correlation between initial DNA damage repair rate and SF₂.