Despite recent advances in the detection and treatment of early stage prost
ate cancer, there remains little effective therapy for patients with locall
y advanced and/or metastatic disease. Although the majority of patients wit
h advanced disease respond initially to androgen ablation therapy, most go
on to develop androgen-independent tumors that are inevitably fatal. Theref
ore, understanding the mechanisms by which a hormone-sensitive tumor escape
s hormonal control is critical to the development of effective therapeutic
modalities. The study of the differentiation pathways of normal and abnorma
l prostate growth has led to the development of a stem cell model for prost
ate cancer [1-3]. Recent work discussed in this commentary suggests that pr
ostate tumors resist apoptosis and proliferate by adopting features of norm
al prostatic stem/progenitor cells. Basal cells, the putative stem/progenit
or cells of the prostate, possess the phenotype of androgen-independence as
do most advanced prostate cancers. Therefore, the study of basal cells may
prove critical to understanding prostate carcinogenesis and to the develop
ment of novel strategies for preventing and managing prostate cancer.