QUANTITATIVE IMMUNOHISTOCHEMICAL DETERMINATION OF CATHEPSIN-D LEVELS IN PROSTATIC-CARCINOMA BIOPSIES - CORRELATION WITH TUMOR GRADE, STAGE,PSA LEVEL, AND DNA-PLOIDY STATUS
Js. Ross et al., QUANTITATIVE IMMUNOHISTOCHEMICAL DETERMINATION OF CATHEPSIN-D LEVELS IN PROSTATIC-CARCINOMA BIOPSIES - CORRELATION WITH TUMOR GRADE, STAGE,PSA LEVEL, AND DNA-PLOIDY STATUS, American journal of clinical pathology, 104(1), 1995, pp. 36-41
National screening programs resulting in an increased detection rate o
f prostatic adenocarcinoma have prompted the search for new methods of
predicting disease outcome that can be applied to the initial narrow
bore needle biopsy specimens. Cathepsin D, a lysosomal aspartyl protea
se and autocrine mitogen, has been studied in a wide variety of human
neoplasms as an invasion and metastasis marker. Prostatic carcinoma ne
edle biopsy tumor cell cathepsin D content was measured in 61 men usin
g a semiquantitative image analysis assisted immunohistochemical proce
dure, Results were compared with preoperative serum prostatic specific
antigen levels, tumor grade, DNA ploidy status, pathologic stage afte
r radical prostatectomy and disease recurrence during a median 2.6 yea
r follow-up. Biopsy cathepsin D levels significantly correlated with t
umor grade (P = .022) and DNA ploidy status (P = .028) by logistic reg
ression analysis. Post-prostatectomy pathologic stage and disease recu
rrence did not correlate with tumor cathepsin D levels, Final prostate
ctomy grade and DNA ploidy status independently predicted metastasis a
nd post-operative disease recurrence (P < .001). Although this study d
id not find independent prognostic status for cathepsin D in prostate
cancer, the correlation with tumor grade and DNA ploidy status is note
worthy and the inter-relationship of outcome variables may prove of in
terest and warrant further evaluation of this potential predictor or C
O-predictor of disease outcome.