We analysed p53 mutations in 24 patients with myelodysplastic syndrome
(MDS) and overt acute myeloid leukaemia after a period of MDS, using
polymerase chain reaction-single strand conformation polymorphism anal
ysis. In exons 5 to 8, mobility shifts were detected in five of the 24
patients. Sequence analysis was subsequently performed, and four miss
ense mutations (16.7%) and one silent nucleotide substitution were ide
ntified. Patients harbouring mutations were characterized as having ad
vanced disease. Loss of the wild type allele was observed in three of
the four patients with missense mutations. No mobility shifts of the N
-ras or FMS gene were detected in these four patients. We next analyse
d the correlation of the p53 mutations with the progression of MDS in
three patients. The mutation was accompanied by the progression in two
of the three patients. These findings suggest that mutations of the p
53 gene are associated with progression in some cases of MDS, while be
ing compatible with stable disease or clonal evolution in others.