The ability to identify individuals at greatest risk of developing lung can
cer can significantly enhance the efficacy of intervention modalities. One
strategy for identifying these individuals is through biomarkers that refle
ct the severity of their cancer. In the present study, we evaluated 22 lung
cancer patients and 35 controls to determine whether the frequency of chro
mosome aberrations was significantly associated with specific clinical vari
ables such as the histological type, grade and stage of the turners. Chromo
some aberrations (expressed as total breaks) were investigated on chromosom
e 1 in interphase nuclei obtained from blood Lymphocytes of the study parti
cipants using the fluorescence in situ hybridization (FISH) chromosome aber
ration assay. Our results indicate a significant linear increase (P = 0.01)
in the level of breaks with respect to the grade of the carcinoma. The poo
rly differentiated tumors had a significantly higher level of chromosome br
eaks mean +/- SD (1.7 +/- 0.46) as compared to the well differentiated tumo
rs (0.98 +/- 0,23, P < 0,05). These results indicate that chromosome aberra
tions, as determined by the FISH assay, can be used as a biomarker for iden
tifying individuals with aggressive types of lung cancer and potentially, a
s a predictor for prognostic outcome of the disease. (C) 2000 Elsevier Scie
nce Ireland Ltd. All rights reserved.