Clinical studies suggest that African-American (AA) prostate cancer patient
s manifest a more aggressive form of the disease compared with white prosta
te cancer patients. However, the biological underpinnings of this potential
difference remain unresolved. To address this issue, we used specific quan
titative immunostaining protocols to determine whether a panel of biomarker
s related to apoptosis including caveolin-1, bcl-2, p53, and c-myc were dif
ferentially expressed in AA versus white prostate cancer patients with simi
lar clinical and pathological characteristics. We further attempted to corr
elate biomarker positivity with proliferation-related markers including Ki-
67 labeling index and apoptotic index. Interestingly, our results indicated
that only the incidence of caveolin-1 staining was significantly different
between these two ethnic/racial groups of prostate cancer patients. The in
cidence of caveolin-1 staining in white patients was 17% compared with 39%
in AA patients (P = 0.0048; Fisher's exact test). In addition, the percenta
ge of caveolin-1-positive prostate cancer cells was also higher in moderate
ly differentiated (Gleason score 6) prostate cancer patients in AA versus w
hites. Because caveolin-1 has been shown previously to demonstrate antiapop
totic activities in prostate cancer cells, our results suggest that differe
nces in caveolin-1 expression may in part underlie the apparent differences
in the clinical virulence of this disease in AA versus white prostate canc
er patients.