In this study we used a unique collection of type specific anti-lamin antib
odies to study iamin expression patterns in normal human skin and in skin d
erived from patients with basal cell carcinomas (BCCs). Lamin expression in
serial sections from frozen tissue samples was investigated by single and
double indirect immunofluorescence. In normal skin, lamin A was expressed i
n dermal fibroblasts and in suprabasal epithelial cells but was absent from
all basal epithelial cells. Lamin C was expressed in dermal fibroblasts, s
uprabasal epithelial cells and a majority of basal epithelial cells. Howeve
r, lamin C was not expressed in quiescent basal epithelial cells. Lamin B-1
was expressed in all epithelial cells but was not expressed in dermal fibr
oblasts. Finally, lamin B-2 was expressed in all epithelial cells but was n
ot expressed in dermal fibroblasts. Finally, lamin B-2 was expressed in all
cell types in normal skin. Lamin expression was also investigated in a col
lection of 16 BCCs taken from a variety of body sites, Based upon patterns
of lamin expression the BCCs were classified into four groups: A-negative (
10/16 rumours), C-negative (5/16 tumours), A/C-negative (1/16 tumours) and
A/B-2-negative (1/16 tumours). Lamin expression was also compared to cell p
roliferation index by staining serial sections with the proliferation marke
r Ki67. 9/10 of the lamin A negative tumours were highly proliferative, whe
reas 4/5 of the iamin C negative tumours were slow growing. Thus as a gener
al rule absence of lamin A was correlated with rapid growth within the tumo
ur, while absence of lamin C was correlated with slow growth within the tum
our. Our data supports the hypothesis that lamin A has a negative influence
on cell proliferation and its down regulation may be a requisite of tumour
progression. (C) 2001 Cancer Research Campaign.