L. Davico et al., Chromosome 8, occupational exposures, smoking, and acute nonlymphocytic leukemias: A population-based study, CANC EPID B, 7(12), 1998, pp. 1123-1125
In a previous epidemiological study on acute myelocytic leukemia (M, M, Cra
ne et at, Cancer Epidemiol, Biomark, Prev., 5: 639-644, 1996), clonal aberr
ations in chromosome 8 have been reported to be in excess in smokers and in
workers exposed to paints. In that study, cytogenetics was performed after
therapy. In our report, we describe a population-based survey on nonlympho
cytic leukemias in northern Italy, in which 79 patients (acute myelocytic l
eukemia, myelodysplastic syndromes, or other nonlymphocytic leukemias) were
studied before cytotoxic therapy. We found 9 aberrations involving chromos
ome 8 (six +8, two -8, and one translocation), whereas abnormalities involv
ing chromosomes 5 and 7 occurred with a low frequency compared with previou
s studies. Aberrations involving chromosome 8 were associated with smoking
(odds ratio, 6.3; 95% confidence interval, 0.9-42.3; among smokers of 10 or
more cigarettes/day: odds ratio, 14.2; 95% confidence interval, 1.4-1423);
+8 aberrations were found in 1 of 24 nonsmokers and in 5 of 38 smokers. Th
ree +8 aberrations were found in 22 subjects potentially exposed to solvent
s or polycycIic aromatic hydrocarbons. The low frequency of chromosome 5 an
d 7 aberrations in our population-based series (compared with other studies
) can be attributed to the recruitment before cytotoxic therapies. Aberrati
ons involving chromosome 8 (particularly +8) were associated with smoking h
abits. Chromosome 8 includes the c-myc oncogene.