G. Lievano et al., ANTITUMOR EFFECT OF CPT-11, A NEW DERIVATIVE OF CAMPTOTHECIN, AGAINSTHUMAN PROSTATE-CANCER (PC-3) IN-VITRO AND PROSTATE RAT-TUMOR (AT-3) IN-VIVO, Methods and findings in experimental and clinical pharmacology, 18(10), 1996, pp. 659-662
In an effort to evaluate the efficacy of CPT-11 on prostate cancer we
utilized the PC-3 human prostate cancer cell line (in vitro), and the
Dunning R3327 AT-3 rat prostate cancer tumor line (in vivo), PC-3 cell
s were initially seeded and cultured prior to the addition of CPT-11 a
t different concentrations 48 and 120 h later. After and additional 48
h the number of cells was determined using MTT dye uptake. CPT-11 at
concentrations between 10 ng/ml and 50 mu g/ml inhibited the growth of
the PC-3 prostate human cancer cell line (p < 0.001). AT-3 prostate r
at cancer cells were injected into the right flank of 30 Copenhagen X
Fischer rats, divided into treated and control groups. A total dose of
CPT-11 (200 mg/kg) was given intraperitoneally, administered 1, 3 and
5 days postimplantation. We evaluated tumor growth by size and weight
(5 and 10 days postimplantation). A total dose of 200 mg/kg inhibited
the rapid growth of the prostate AT-3 tumor in vivo (p < 0.001).