PMID- 16546907 OWN - NLM STAT- MEDLINE DCOM- 20060601 LR - 20191210 IS - 0955-3002 (Print) IS - 0955-3002 (Linking) VI - 82 IP - 2 DP - 2006 Feb TI - Evaluation of spectral karyotyping (SKY) in biodosimetry for the triage situation following gamma irradiation. PG - 87-96 AB - PURPOSE: Biological dosimetry in an acute triage situation of radiation exposure is traditionally performed by scoring unstable dicentric chromosomal aberrations after conventional Giemsa staining, and more recently also by detection of chromosomal translocations after chromosome painting by fluorescence in situ hybridization (FISH). By spectral karyotyping (SKY) each chromosome can be painted in an individual colour, permitting the scanning for structural aberrations throughout the genome in each individual metaphase. Here we have evaluated the performance of SKY analysis in a simulated triage situation after gamma irradiation. MATERIALS AND METHODS: Peripheral leukocytes were irradiated by 60Co (0 - 5 Gy) and analysed by SKY, Giemsa staining and FISH painting of chromosomes 1, 2, and 3. RESULTS: At 1 Gy and higher doses, dicentric aberrations (Dic+) as well as classical one- and two-way translocations were found in increasing and dose-dependent frequencies by SKY. The frequency of dicentrics detected by Giemsa was found to be significantly higher than the total aberrations detected by SKY (p<0.001), but did not differ significantly from that of FISH painting. The difference was mainly attributable to the low sensitivity of SKY to detect Dic+ following frequent lack of acentric fragments with matching chromosomal composition. CONCLUSIONS: The findings anticipate that radiation induced chromosomal aberrations may be more complex than expected from conventional and single chromosome painting analyses. While conventional Giemsa staining was found to be the method of choice for the triage situation, it is expected that extended SKY analysis will add to the knowledge of underlying mechanisms for irradiation associated chromosomal aberrations. FAU - Szeles, Anna AU - Szeles A AD - Department of Oncology-Pathology, Karolinska University Hospital-Solna, Stockholm, Sweden. FAU - Joussineau, Sigfried AU - Joussineau S FAU - Lewensohn, Rolf AU - Lewensohn R FAU - Lagercrantz, Svetlana AU - Lagercrantz S FAU - Larsson, Catharina AU - Larsson C LA - eng PT - Comparative Study PT - Evaluation Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Int J Radiat Biol JT - International journal of radiation biology JID - 8809243 SB - IM MH - Biological Assay/methods MH - Cells, Cultured MH - Chromosome Aberrations/*radiation effects MH - Chromosomes/*radiation effects MH - Humans MH - Leukocytes/*pathology/*radiation effects MH - Male MH - Middle Aged MH - Radiation Dosage MH - Radiometry/*methods MH - Reproducibility of Results MH - Risk Assessment/methods MH - Risk Factors MH - Sensitivity and Specificity MH - Spectral Karyotyping/*methods MH - Triage/*methods EDAT- 2006/03/21 09:00 MHDA- 2006/06/02 09:00 CRDT- 2006/03/21 09:00 PHST- 2006/03/21 09:00 [pubmed] PHST- 2006/06/02 09:00 [medline] PHST- 2006/03/21 09:00 [entrez] AID - K108828408R91530 [pii] AID - 10.1080/09553000600599767 [doi] PST - ppublish SO - Int J Radiat Biol. 2006 Feb;82(2):87-96. doi: 10.1080/09553000600599767.