Mutation in the p53 tumor suppressor gene is the most common genetic a
lteration in human cancer. As in mutant p53 the protein is stabilised
and the half-life is extended, it becomes detectable by immunohistolog
ical staining. p53 immunoreactivity thus seems to be a potential bioma
rker for the assessment of the oncogenic potential of malignant melano
mas. In 103 tissue sections of primary and metastatic malignant melano
mas of the head and neck detectable levels of p53 were only found in 3
of the primary tumors and in none of the metastases. At the same time
the proliferation status of the malignant melanoma lesions was determ
ined using the cell cycle specific antibody PCNA. 55 primary and metas
tatic tumors were stained with a PCNA-MAb to determine the proliferati
on activity of the tumors. The results of our immunohistochemical inve
stigation suggest that immunoreactivity of p53 cannot be used to deter
mine the malignant potential of melanomas in the head and neck. PCNA s
taining showed that the majority of the tumors and metastases were pro
liferating rapidly.