Epidemiological studies have shown that inhalation of radon, a radioactive
gas, is associated with an increased risk for lung cancer. We have develope
d a model of radon-induced rat lung tumors to characterize cytogenetic and
molecular events involved in radon-induced lung tumorigenesis. Using compar
ative genomic hybridization (CGH), gains and losses of genetic material wer
e investigated in a series of 13 carcinomas and four adenomas of the lung.
Frequent losses occurred at 4q12-21, 5q11-33, and 15q, which are homologous
to human chromosome (HSA) bands 7q21-36, 1p31-36/9p21-31, and 13q14.1-14.3
/3p14.2, respectively. These regions are frequently (30-80%) deleted in hum
an lung cancer acid contain tumor suppressor genes or proto-oncogenes such
as MET, CDKN2A/p16IMTSI, CDKN2B/p 15/MTS2, FHIT, and RBI or yet to be ident
ified genes. Frequent gains involved 6, 7q34-qter, and 19q; chromosomes 6 a
nd 7 being homologous to human 2p21-25 and 8q21-24 where the MYCN and MYC o
ncogenes are located. The genetic similarities between rat and human lung c
ancer suggest common underlying mechanisms for tumor evolution in both spec
ies. Moreover, cytogenetic and molecular genetic analyses of radon-induced
rat lung tumors could help to better understand the development and progres
sion of radon-induced lung cancer in man. Genes Chromosomes Cancer 29:1-8,
2000. (C) 2000 Wiley-Liss, Inc.