Prostate cancer progresses from a localized disease to a widely disseminated malignancy. Each step along this progression pathway involves multiple genetic alterations that impart a survival advantage to the tumor cell over its normal counterparts and may confer resistance to therapy. Because metastatic prostate cancer is one of the most therapy-resistant human neoplasms, we studied the expression of certain molecular determinants of drug resistance in the context of tumor progression. Paraffin-embedded formalin-fixed resected prostates were chosen based on Gleason grade and surgical stage. Immunohistochemistry was used to detect the expression of multidrug resistance protein (MRP), topoisomerase IIα, p53, glutathione S- transferase π, Bcl-2, and P-glycoprotein in these specimens. We found that all of the proteins were expressed in resected prostate except for P- glycoprotein. The expression of MRP, topoisomerase IIα, p53, and Bcl-2 increased with the Gleason grade. In addition, the expression of MRP, topoisomerase IIα, and p53 increased with the surgical stage. In contrast, the glutathione S-transferase π and Bcl-2 expression decreased with the increasing surgical stage. Stage was the strongest indicator of protein expression. These results suggest that drug resistance gene products are expressed in prostate cancer at the time of surgical resection. Thus, although the emergence of the 'pan-resistance' phenotype in prostate cancer may partly be a function of the selection pressure exerted by therapeutic interventions, certain determinants of chemoresistance may he caused by genetic changes accompanying tumorigenesis.
|Original language||English (US)|
|Number of pages||11|
|Journal||Clinical Cancer Research|
|State||Published - Jun 1 1998|
All Science Journal Classification (ASJC) codes
- Cancer Research