There is a growing body of evidence suggesting that alterations in the adhe
sion properties of neoplastic cells may play a pivotal role in the developm
ent and progression of bladder cancer. Loss of intercellular adhesion and t
he desquamation of cells from the underlying lamina propria allows malignan
t cells to escape from their site of origin, degrade the extracellular matr
ix, acquire a more motile and invasive phenotype, and finally invade and me
tastasize. In addition to participating in tumor invasiveness and metastasi
s, adhesion molecules regulate or significantly contribute to a variety of
functions, including signal transduction, cell growth, differentiation, sit
e-specific gene expression, morphogenesis, immunologic function, cell motil
ity, wound healing, and inflammation. To date, a diverse system of transmem
brane glycoproteins have been identified that mediate the cell-cell and the
cell-extracellular matrix adhesion. The main families of adhesion molecule
s are the cadherins, integrins, members of the immunoglobulin superfamily,
and selectins. We review the recent data regarding the role of selected adh
esion molecules in the pathogenesis of bladder cancer and their clinical ex
ploitation as biomarkers of this malignant disease. (C) 1999, Elsevier Scie
nce Inc. All rights reserved.