Optimizing chemical-induced premature chromosome condensation assay for rapid estimation of high-radiation doses.

Abstract

In the event of exposure to high doses of radiation, prompt dose estimation is crucial for selecting appropriate treatment modalities, such as cytokine therapy or stem cell transplantation. The chemical-induced premature chromosome condensation (PCC) method offers a simple approach for such dose estimation with significant radiation exposure, but its 48-h incubation time poses challenges for early dose assessment. In this study, we optimized the chemical-induced PCC assay for more rapid dose assessment. A sufficient number of PCC and G2/M-PCC cells were obtained after 40 h of culture for irradiated human peripheral blood up to 20Gy. By adding caffeine (final concentration of 1 mM) at 34 h from the start of culture, G2/M-PCC index increased by 1.4-fold in 10Gy cultures. There was also no significant difference in the G2/M-PCC ring frequency induced for doses 0 to 15Gy between our 40-h caffeine-supplemented chemical-induced PCC method and the conventional 48-h PCC assay.