Epidemiological and experimental studies have suggested the enhancement of
asbestos-induced disease processes by simultaneous exposure to kerosene, it
s soot, and cigarette smoke in asbestos-exposed animals as well as in human
s. To determine the influence of these factors on the genotoxic potential o
f asbestos, a micronucleus lest was performed in Syrian hamster embryo fibr
oblasts (SHE) and human lymphocytes. To observe the specific chromosomal da
mages, multicolor fluorescence in situ hybridization (FISH) was done in the
lymphocytes from smokers and nonsmokers exposed in vitro to asbestos. Sign
ificantly higher numbers of micronuclei were observed in SHE cells after co
mbined treatment with chrysotile and kerosene soot (111 micronuclei/1000 ce
lls) in comparison to chrysotile and kerosene soot separately. kinetochore
staining revealed mainly clastogenic effects in all the cases. In human lym
phocytes exposed in cultures to chrysotile and crocidolite the numbers of m
icronuclei were found higher in smokers than nonsmokers. Multicolor FISH as
say suggested that asbestos fibers inflict high damage within 1q12 and in t
he region between 1 cen and 1q12 of chromosome 1. In the exposed population
of an asbestos cenment factory: the highest generic damage was found in th
e blood lymphocytes of exposed smokers. The study suggests that smokers occ
upationally exposed to asbestos and domestically to kerosene soot are at hi
gher risk for the early development of asbestos-induced diseases.