Fas (Apo-1/CD95) is a cell-surface receptor involved in cell death signalin
g. The key role of the Fas system in negative growth regulation has been st
udied mostly within the immune system, and somatic mutations of Fas in cant
er patients have been described solely in lymphoid-lineage malignancies. We
analyzed somatic mutations and loss of heterozygosity of Fas gene in 43 tr
ansitional cell carcinomas of urinary bladder. Overall, 12 tumors (28%) wer
e found to have Fns mutations, including 11 missense mutations and 1 frames
hift mutation. Ten of the 12 mutations were located in the death domain kno
wn to be involved in the transduction of an apoptotic signal, and 8 of thes
e 10 mutations showed an identical G to A transition at bp 993, indicating
a potential hotspot in bladder cancers. Three of eight (38%) informative tu
mors carrying Fas mutations showed LOH at polymorphic sites in the promoter
region. This is the first report on the Fas gene mutations in nonlymphoid
malignancies, and our data suggest that alterations of the Fas gene might l
ead to the loss of its apoptotic function and contribute to the pathogenesi
s of some bladder cancers.