EXPRESSION AND TOPOGRAPHY OF INTEGRINS AND BASEMENT-MEMBRANE PROTEINSIN EPIDERMAL CARCINOMAS - BASAL BUT NOT SQUAMOUS-CELL CARCINOMAS DISPLAY LOSS OF ALPHA-6-BETA-4 AND BM-600 NICEIN
P. Savoia et al., EXPRESSION AND TOPOGRAPHY OF INTEGRINS AND BASEMENT-MEMBRANE PROTEINSIN EPIDERMAL CARCINOMAS - BASAL BUT NOT SQUAMOUS-CELL CARCINOMAS DISPLAY LOSS OF ALPHA-6-BETA-4 AND BM-600 NICEIN, Journal of investigative dermatology, 101(3), 1993, pp. 352-358
The expression and topography of some integrins and basement membrane
proteins in cutaneous basal cell carcinomas (BCCs) and squamous cell c
arcinomas (SCCs) have been studied by immunohistochemistry and Western
blotting. it has been shown that the typical cell-to-cell distributio
n of alpha2beta1 and alpha3beta1 found in normal epidermis is replaced
by pericellular distribution in both BCC and SCC cells. BCC and SCC a
lso showed different patterns of expression of alpha6beta4, an integri
n heterodimer normally lining the basal surface of basal epidermal ker
atinocytes: whereas SCC showed high expression and pericellular distri
bution of alpha6beta4, BCC cells did not express this integrin at all.
The absence of alpha6 and beta4 subunits from BCC extracts was confir
med by Western blotting. The molecular composition of the basement mem
brane was markedly different in the two types of epidermal tumors. Whe
reas laminin and collagen type IV were conserved in the basement membr
ane zone of both tumors, the molecular complex BM-600/nicein, which is
recognized by the monoclonal antibody GB3 and is possibly identical t
o the previously described basement membrane glycoproteins kalinin and
epiligrin, was absent from BCC cells. Then, the simultaneous loss of
expression of alpha6beta4 and BM-600/nicein in BCC cells but not in SC
C cells indicates that alpha6beta4 integrin and one of its potential l
igands may be co-regulated in both BCC and SCC, thus suggesting a role
for this phenomenon in the pathogenesis and clinical behavior of thes
e epidermal tumors.