During prostate cancer progression, invasive glandular epithelial cells mov
e out of the ductal-acinar architecture and through the surrounding basemen
t membrane, Extracellular matrix proteins and associated soluble factors in
the basal lamina and underlying stroma are known to be important regulator
s of prostate cell behaviors in both normal and malignant tissues. In this
study, we assessed cell interactions with extracellular matrix and stromal
factors during disease progression by characterizing integrin usage and exp
ression in a series of parental and lineage-derived LNCaP human prostate ca
ncer cell lines. Although few shifts in integrin expression were found to a
ccompany disease progression, integrin heterodimer usage did change signifi
cantly. The more metastatic sublines were distinct in their use of alpha (v
)beta (3) and, when compared with parental LNCaP cells, showed a shift in a
lpha (6) heterodimerization, a subunit critical not only for interaction wi
th prostate basal lamina but also for interaction with the bone matrix, a f
avored site of prostate cancer metastases.