Background: In order to clarify the relationship between delayed reproducti
ve death and radiation-induced genomic instability, the colony-forming effi
ciency of surviving, irradiated human squamous carcinoma cells and centrome
re positive as well as centromere negative micronuclei in surviving progeny
were examined.
Materials and methods: Colony-forming ability and micronucleus (MN) frequen
cy in binucleated cells 24 h after the addition of cytochalasin B during 2
weeks of post-irradiation growth were determined in a squamous cell carcino
ma cell line (SCL-II) of human origin. In addition, centromeres in micronuc
lei were detected using FISH.
Results: In the human epithelial cell line used for these experiments, dela
yed reproductive death was pronounced and persisted for at least 2 weeks af
ter irradiation. Although there is evidence for an increased rate of centro
mere positive micronuclei, but not of centromere negative micronuclei, aris
ing during the first week of post-irradiation proliferation, this decreases
later while the rate of delayed reproductive death remains elevated.
Conclusion: In the studied cell line, the observed delayed reproductive dea
th is not closely related to the investigated criteria of radiation-induced
genomic instability. This casts doubt on the common assumption that delaye
d reproductive death is a direct manifestation of radiation-induced genomic
instability.