Prostate cancer (PCA), the most commonly diagnosed cancer in males in the U
nited States, is the second leading cause of cancer-related deaths of males
in this country. Because of the poor success rate in the treatment of PCA,
an intervention at an early stage may reduce the progression of small carc
inoma to large metastatic lesion, thereby reducing PCA-related deaths. Conc
erted efforts are needed to establish mechanism-based approaches to develop
: (a) the markers for early detection of the disease as well as toward moni
toring the efficacy of treatment(s); and (b) novel chemopreventive strategi
es against PCA. Using unique samples of pair-matched benign and cancer tiss
ue obtained from the same PCA patient, we showed that ornithine decarboxyla
se (ODC) activity is significantly (P < 0.001) elevated in PCA (1142 +/- 10
0; mean +/- SE) than in paired benign tissue (427 +/- 51; mean +/- SE). The
immunoblot analysis also showed a significant elevation in the protein exp
ression of ODC in the PCA tissues as compared with the paired benign tissue
. Furthermore, our data showed that the ODC activity in the prostatic fluid
obtained by a digital rectal massage from the patients with PCA (3847 +/-
162; mean +/- SE) was significantly higher than in the patients with benign
prostatic hyperplasia (2742 +/- 167; mean +/- SE) or normal individuals (1
244 +/- 67; mean +/- SE). This observation might be of significance because
the prostatic fluid could be obtained noninvasively by digital rectal mass
age. We suggest that ODC could serve as a target for early detection of hum
an PCA as well as for monitoring the efficacy of treatment(s). The developm
ent of ODC as a target for novel chemopreventive strategies against PCA is
an intriguing possibility.