TY - JOUR
T1 - Evaluation of the cancer chemopreventive efficacy of silibinin in genetic mouse models of prostate and intestinal carcinogenesis
T2 - Relationship with silibinin levels
AU - Verschoyle, Richard D.
AU - Greaves, Peter
AU - Patel, Ketan
AU - Marsden, Debbie A.
AU - Brown, Karen
AU - Steward, William P.
AU - Gescher, Andreas J.
N1 - Funding Information:
Supported by Cancer Research UK programme grant C325/A6691 and UK Medical Research Council programme grant G0100874. The authors thank Dr. Paolo Morazzoni, Indena Spa., Milan, Italy, for generous provision of silipide, Mrs. J. Edwards (MRC Toxicology Unit, University of Leicester) for help with the histology, and the staff in the Leicester University Biomedical Services facility for help with animal husbandry.
PY - 2008/4
Y1 - 2008/4
N2 - Silibinin, a flavonolignan from milk thistle seeds, possesses cancer chemopreventive properties in rodent models of carcinogenesis. We tested the hypotheses that silibinin or silipide, silibinin formulated with phospholipids, delays tumour development in TRAMP or ApcMin mice, genetic models of prostate or intestinal malignancies, respectively. Mice received silibinin or silipide with their diet (0.2% silibinin equivalents) from weaning. Intervention with silipide reduced the size of well differentiated TRAMP adenocarcinomas by 31%. Silipide and silibinin decreased the incidence of poorly differentiated carcinomas by 61% compared to mice on control diet. Silipide decreased plasma levels of insulin-like growth factor (IGF)-1 by 36%. Levels of circulating IGF binding protein (IGFBP)-3 in mice on silipide or silibinin were 3.9- or 5.9-fold, respectively, elevated over those in control TRAMP mice. In ApcMin mice silibinin, but not silipide, had only a marginal adenoma number-reducing effect. The results cautiously support the advancement of silipide to the stage of clinical investigation in prostate cancer.
AB - Silibinin, a flavonolignan from milk thistle seeds, possesses cancer chemopreventive properties in rodent models of carcinogenesis. We tested the hypotheses that silibinin or silipide, silibinin formulated with phospholipids, delays tumour development in TRAMP or ApcMin mice, genetic models of prostate or intestinal malignancies, respectively. Mice received silibinin or silipide with their diet (0.2% silibinin equivalents) from weaning. Intervention with silipide reduced the size of well differentiated TRAMP adenocarcinomas by 31%. Silipide and silibinin decreased the incidence of poorly differentiated carcinomas by 61% compared to mice on control diet. Silipide decreased plasma levels of insulin-like growth factor (IGF)-1 by 36%. Levels of circulating IGF binding protein (IGFBP)-3 in mice on silipide or silibinin were 3.9- or 5.9-fold, respectively, elevated over those in control TRAMP mice. In ApcMin mice silibinin, but not silipide, had only a marginal adenoma number-reducing effect. The results cautiously support the advancement of silipide to the stage of clinical investigation in prostate cancer.
KW - Chemoprevention
KW - IGF
KW - Preclinical models
KW - Silibinin
UR - http://www.scopus.com/inward/record.url?scp=41949087545&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2008.02.020
DO - 10.1016/j.ejca.2008.02.020
M3 - Article
C2 - 18343654
AN - SCOPUS:41949087545
SN - 0959-8049
VL - 44
SP - 898
EP - 906
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 6
ER -