K. Jung et al., ANTIOXIDANT ENZYMES IN MALIGNANT PROSTATE CELL-LINES AND IN PRIMARY CULTURED PROSTATIC CELLS, Free radical biology & medicine, 23(1), 1997, pp. 127-133
The antioxidant enzymes catalase, glutathione reductase(GR), glutathio
ne S-transferase(GST), glutathione peroxidase (GPx), and superoxide di
smutase (SOD) were determined in the androgen-responsive LNCaP and and
rogen-nonresponsive PC-3 and DU 145 cells as well as in prostatic epit
helial cell cultures of benign and malignant human prostatic tissue. T
here were no differences between the enzyme activities of the human pr
imary cell cultures from cancerous tissue and their normal counterpart
s. The enzyme activities of the three permanent cell lines were either
higher (SOD, catalase, GR) or lower (GST, GPx) than in the primary ce
ll cultures. In LNCaP cells catalase and GR were significantly higher,
GST, in contrast, was significantly lower than in PC-3 and DU 145 cel
ls. GST in PC-3 and DU 145 cells, and SOD in all the three cell lines
showed no significant differences. Catalase, GPx and GR values were si
gnificantly different in the three permanant cell lines. The different
enzymatic equipment of the prostate cancer cell lines provides the ba
sis for experimental testing of new concepts of cancer treatment with
the help of systematic modulations of the antioxidant defence systems
in prostate cancer. (C) 1997 Elsevier Science Inc.