Abnormalities in the p53 tumor suppressor gene have been shown to affe
ct cell cycle control and lead to genetic instability in cell lines of
murine and human origin. We have examined genetic instability in 183
primary human breast carcinomas with and without p53 abnormalities. Mu
tation analysis was performed by constant denaturant gel electrophores
is and DNA sequencing, and abnormal protein expression was examined by
immunohistochemical staining methods. Genetic instability was studied
by detection of gene amplification, allelic loss, karyotype analysis,
and fluorescent in situ hybridization. We found a significant associa
tion between p53 abnormalities and genetic instability detected by the
se methods.