We analysed the status of the p53 gene and protein in eight newly establish
ed acute myeloid leukaemia (AML) cell lines representing blast cells of eit
her de novo leukaemia patients in first remission or patients with relapsed
and chemotherapy-resistant disease causing their death. There were no muta
tions in the p53 gene in any of the cell lines as analysed by single-strand
conformation polymorphism of amplified exons 5-8. However, the p53 protein
was clearly and consistently expressed in all of these cell lines, as show
n by immunohistochemistry, Western blotting and flow cytometry. The consist
ently expressed p53 protein was located in both the nucleus and the cytopla
sm of all the cell lines and, as shown by flow cytometry, it was mostly in
a conformation typical of the mutated protein. These AML cell lines offer a
tool for studying the production and function of the p53 protein and its p
ossible role in cell cycle regulation and chemoresistance as well as in the
regulation of apoptosis in AML.