Prostate cancer is the most commonly diagnosed malignancy in the American m
en and the second leading cause of male cancer death in the United States.
Despite its high incidence, the molecular and genetic events involved in pr
ostate cancer progression remain poorly understood. A hurdle in understandi
ng the molecular genetic changes in prostate cancer has been the difficulty
in establishing premalignant lesions and primary prostate tumors as in vit
ro cell cultures. Primary epithelial cells grow for a finite life span and
then senesce. Immortalization is defined by continuous growth of otherwise
senescing cells and is believed to represent an early stage in tumor progre
ssion. In order to examine these early stages, we and others have developed
in vitro models of prostate epithelial cell immortalization. Because prost
ate cancer is a multistep, progressive disease with a typical onset later i
n life and with an unusually high number of latent cases that do not develo
p into clinically manifest cancer, the steps in the progression to malignan
cy are of particular interest. To understand the many factors that are susp
ected to contribute to the development of this malignancy, there is a need
for an in vitro multistep human prostate epithelial (HPE) culture system. T
hese models have been extremely important in identifying genetic and molecu
lar changes involved in prostate cancer progression.