Malignant mesothelioma (MM) is predominantly a sporadic malignancy linked t
o exposure to asbestos. Clustering of MM in families suggests genetic susce
ptibility as a contributing factor. We performed comparative genomic hybrid
ization (CGH) analysis on tumor samples from members of a family with MM of
the pleura and a history of parental cancer. Our specific aim was to find
a recurrent copy number loss indicating the chromosomal area to which a gen
e underlying the development of MM could be assigned according to the Knuds
on two-hit hypothesis. We found losses at 1p, 6q. 9p. 13q, and 14q. The cop
y number changes were very similar to those reported in sporadic cases. Our
findings and results from sporadic cases highlight the importance of cloni
ng the genes in the loss sites at 1p, 6q, 14q, and 22q. (C) 2001 Elsevier S
cience Inc. All rights reserved.