P. Guinan et al., Paclitaxel is more effective than thalidomide in inhibiting LNCaP tumor growth in a prostate cancer model, METH FIND E, 20(9), 1998, pp. 739-742
Citations number
19
Categorie Soggetti
Pharmacology & Toxicology
Journal title
METHODS AND FINDINGS IN EXPERIMENTAL AND CLINICAL PHARMACOLOGY
LNCaP tumors were treated by either administration of paclitaxel, thalidomi
de or by orchiectomy in order to determine their relationship with markers
pertaining to the process of tumor growth,apoptosis or angiogenesis. Forty
mts bearing LNCaP tumors were divided into 4 groups bf 10 and treated by ei
ther paclitaxel (20 mg/kg x 5 days); thalidomide (200 mg/kg x 5 days/week x
5 weeks); or orchiectomy. After 6 weeks serum samples were. removed for PS
A determination and the animals sacrificed for evaluation of:A) tumor volum
e; B) tissue bcl-2, cyclin D, PSA and factor VIII immunohistochemically gra
ded (0-5 scale)for marker expression; and C) serum PSA. Comparisons were ma
de to untreated LNCaP turners. Statistically significant differences were d
etermined using the nonparametric Mann-Whitney test. Paclitaxel produced si
gnificant differences in volume (p < 0.001), expression of bcl-2 (p < 0.043
), cyclin D (p < 0.023), tissue PSA (p < 0.001) and serum PSA (p < 0.019) l
evels. Thalidomide altered expression of bcl-2 (p < 0.011) and tissue PSA (
p < 0.002). Orchiectomy altered volume (p < 0.002) and bcl-2 expression (p
< 0.001). All three therapies have been suggested for prostate cancer and e
ach produced alterations in accepted markers for treatment response (either
reduced volume or serum PSA). Paclitaxel significantly influenced the most
markers. Of interest was that all treatments, especially thalidomide, a kn
own antiangiogenesis agent, reduced factor VIII, although not significantly
Evidently each treatment evokes different pathways of activity. (C) 1998 P
rous Science. All rights reserved.