Mutation and expression of the p53 gene in malignant melanoma cell lines

Three monoclonal antibodies (MAbs) against p53 protein (PAb 24o, DO‐I and Pab1801) were used to define the immunophenotype of 13 melanoma cell lines. Immunoreactions could be detected in 12 out of 13 cell lines by using the indirect immunofluorescence technique. In 7 of these the majority of cells displayed cytoplasmic staining whereas positive nuclei were detected in only a few cells. Two cell lines had predominantly nuclear reactivity, while the remaining 3 cell lines showed signals in both locations. Despite identical nuclear staining patterns, the 3 MAbs produced qualitatively distinct cytoplasmic immunoreactions. PAb240 and DO‐ I, which showed similar staining frequencies, appeared more sensitive in the detection of p53 protein than did PAb 1801. Immunoprecipita‐tions of lysates from each of the cell lines with MAbs DO‐I and 1801 (which bind to both wild‐type and mutant p53 species) detected 53–kDa proteins, whereas PAb240 (which recognizes the mutant conformation of the protein in this type of assay) detected 53–kDa proteins in only 4 cell lines. Nucleotide sequencing of exons 5 to 9 of TP53 in these latter cell lines showed that each has homozygous point mutations in the locus, whereas in the others no TP53 alterations were found. Three of the 4 mutations were C‐to‐T transversions, alterations possibly caused by damage from UV‐light. Our findings indicate that immunostaining with p53 antibodies, although common in malignant melanoma, results from the presence of mutant p53 protein in about 30% of the cases tested. Neither immunostaining with PAb240 nor the patterns of intracellular distributions of the signals are sufficient to detect TP53 mutations.