Objectives. To assess the levels of caveolin-1 in a Series of bladder tumor
specimens of varying stage and grade and to identify possible links betwee
n caveolin-1 status and clinical behavior. Caveolae have emerged as sites o
f important regulatory events at the cell membrane in many different cell t
ypes. Caveolins are the main structural components of caveolae and belong t
o a family of highly conserved integral membrane proteins. The function of
caveolin-1 appears to be intrinsically linked to cell signaling modulation
by multiple pathways. Modification of CAV-1 gene expression appears, to be
a common feature of the oncogenically transformed phenotype.
Methods. Using a rabbit polyclonal antibody, against caveolin-1 and immunoh
istochemistry, we assessed caveolin-1 protein expression in 89 formalin-fix
ed, paraffin-embedded bladder tumor sections. The patient group studied inc
luded 71 men and 18 women (mean age +/- SD 69.7 +/- 10.9 years). The stage
was Ta-T1 in 68 and T2-T4 in 21 tumors in this series. The clinical follow-
up was 1 to 38 months (mean 21.2 +/- 9.9).
Results. A statistically significant association was observed between caveo
lin-1 immunoreactivity and tumor grade (P = 0.0118, chi-square test), with
8 (21%) of 38 G3, 1 (3%) of 30 G2, and 0 of 21 G1 tumors positive for caveo
lin-1. When the clinical data were examined in conjunction with caveolin-1
status, no statistically significant relationship was seen between caveolin
-1 expression and tumor multiplicity, tumor recurrence, tumor progression,
or patient survival.
Conclusions. The results of our study demonstrate that altered expression o
f caveolin-1 protein is a component of tumor dedifferentiation in a subset
of high-grade bladder cancers. This pilot study provides a basis for furthe
r investigation of the role of caveolin-1 and the function of caveolae in t
he most aggressive forms of this tumor. (C) 2001, Elsevier Science Inc.