Prostate cancer is the most common cancer in American men and the second le
ading cause of cancer deaths in this group. We have found that interleukin
(IL)-6 protein concentrations are increased similar to 18-fold in clinicall
y localized prostate cancers when compared to normal prostate tissue. Norma
l and neoplastic prostatic epithelial cells in culture, with the exception
of LNCaP cells, secrete IL-6. Addition of exogenous IL-6 to primary epithel
ial cells in culture or the LNCaP prostate cancer cell line leads to phosph
orylation of Stat-3 and increases in net cell proliferation. The concentrat
ion of IL-6 receptor is increased eightfold in the prostate cancer tissues
and is increased in the cancer cells by immunohistochemistry. The increased
expression of IL-6 receptor is correlated with increased proliferation of
prostate cancer cells in vivo as assessed by Ki67 immunohistochemistry. The
se findings strongly support the hypothesis that IL-6 acts as a significant
autocrine growth factor in vivo for primary, androgen-dependent prostate c
ancers.