Prostate cancer is a multistep process in which progression rather than ini
tiation may be the rate-limiting step. A strong possibility is that prostat
ic intraepithelial neoplasia lesions that switch to angiogenic phenotype ev
entually progress to cancer. However, it is a challenging task to quantitat
e angiogenesis in preneoplastic lesions. A promising approach to measuring
angiogenesis involves real-time TaqMan polymerase chain reaction to quantit
ate mRNAs encoding a panel of angiogenesis markers. This highly sensitive m
olecular technique has potential for quantitating angiogenesis in clinical
settings and can be used as a high-throughput screening procedure in prosta
te cancer clinical trials.