Background: p53 is a tumor suppressor nucleoprotein. Mutations of the
p53 gene have been found in a variety of malignant neoplasms. Wild-typ
e p53 has a short half-life, possibly only 20 to 30 minutes, and is no
t present in the nucleus at levels that are detectable with routine im
munohistochemical techniques. Mutant p53 has a longer half-life, and i
s readily detectable with immunoperoxidase staining. Results: We studi
ed 17 specimens from patients with either porokeratosis of Mibelli or
actinic porokeratosis, using immunoperoxidase staining with an antibod
y directed against the p53. There was staining of lesional keratinocyt
e nuclei in 16 of 17 specimens, limited in most cases to the zone betw
een carnoid lamellae. Staining for proliferating cell nuclear antigen
was increased above background levels in only six of 13 specimens. Con
clusions: The finding of p53 immunoperoxidase staining in porokeratosi
s suggests genetic mutation, as occurs in other cutaneous keratinocyti
c neoplasms, and the lack of corresponding proliferating cell nuclear
antigen expression in many specimens indicates that p53 overexpression
is not simply a reflection of increased cellular proliferation.