Recently, a novel tumor suppressor gene, p73, was isolated and mapped to ch
romosome 1p36, a region commonly associated with loss of heterozygosity in
neuroblastoma and other human malignancies, including breast cancer. The p7
3 gene shares considerable homology with the common tumor suppressor gene p
53, both in composition and function. This study examines the potential par
ticipation of p73 in the pathogenesis of sporadic and hereditary breast can
cers. Mutation analysis of 29 hereditary breast cancer cases revealed five
independent silent mutations in the hereditary cases that are unlikely to p
lay a role in tumor development. Mutation analysis of 48 sporadic breast tu
mors did not identify any unique variants. Eleven common polymorphisms scat
tered throughout the gene were also detected. Thus, mutations in the p73 ge
ne appear to play little if any role in hereditary or sporadic breast cance
r.