Reduction or absence of cell-cell adhesion molecules has been reported in v
arious carinomas and the abnormal expression of these molecules contributes
to the invasive and metastatic behavior of malignant tumor cells. In epide
rmal keratinocytes, the main cell-cell adhesion systems are adherens juncti
ons and desmosomes. Previous studies have shown that, in skin carcinomas, t
he decreased expression of E-cadherin, major constitutional glycoprotein of
adherens junctions, is associated with the invasive and metastatic ability
of the tumor cells. In the present study, we examined the expression of de
smoglein I and plakoglobin, the constitutional components of desmosomes, in
various skin carcinomas such as basal cell carcinoma (BCC), squamous cell
carcinoma (SCC), extramammary Paget's disease and Bowen's disease by an imm
unofluorescence method. In normal human skin, desmoglein I and plakoglobin
were strongly expressed in the intercellular space of the epidermis except
for the basal cell layer. In BCC and SCC, the expression of desmoglein I an
d plakoglobin was markedly reduced or absent in tumor cells. In carcinoma i
n situ of Paget's disease, compared with the normal epidermal cells surroun
ding tumor cell nests, the expression of these molecules was reduced in tum
or cells. In Paget's disease with dermal infiltration of tumor cells, the e
xpression of these molecules was almost absent throughout the epidermis. In
Bowen's disease, the expression of desmoglein I was reduced in the clumpin
g cells and dyskeratotic cells. These results suggest that the expression o
f desmosomal cadherin is reduced or absent in human skin carcinomas, and th
at reduction of these molecules may also contribute to the invasiveness and
metastasis of skin carcinomas.