Prostate cancer is the second leading cause of cancer-related deaths in the
United States. However, the underlying molecular events for prostate cance
r development are not clear. In this study, we applied the recently develop
ed technology known as differential subtraction chain (DSC) to identify a n
ovel gene whose expression is inactivated in high grade prostate cancer. Th
is gene, designated as SAPC, is expressed in normal prostate acinar cells.
Its expression is dramatically down-regulated in high grade prostate cancer
s (4/4) but is unaltered in low grade prostate cancers. It encodes a 7.7-kd
protein. Its sequence shares some homology with the cysteine-rich domain o
f 2-5A-dependent RNase L,which is a critical component of the interferon-in
duced apoptosis cascade. The selective inactivation in the more aggressive
prostate cancers holds promise for SAPC as a potential prognostic marker fo
r high grade prostate cancer.