Korean J Urol.
2001 Jun;42(6):663-667.
Allium Sativum-mediated Therapy for Experimental Prostate Cancers with In Vivo Tumor Transduction: Effects on Tumor Growth and Development
- Affiliations
-
- 1Department of Urology, Seoul Adventist Hospital and Korea University
Hospital, Seoul, Korea.
Abstract
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PURPOSE: Allium sativum (AS) has been known to have widespread benefits in reducing
some human cancer risk by immune stimualtion and anticarcinogenic activity. In the
present study, we evaluated the preventive and antitumor properties of AS as an
effective anticancer modifier for human prostate cancer in vivo.
MATERIALS AND METHODS
Subcutaneous prostate cancers were established in athymic
nude mice with 5x10(5) PC-3 human androgen-indenpendent prostate cancer cells. AS
was injected at the site of tumor transplantation on day 1 and one week intervals
up to 5 weeks (Experiment I), and into the established tumors sized by 50-60mm(3)
weekly for 5 weeks (Experiment II). Therapeutic responses and efficacies of AS for
prostate cancers in vivo were determined in separate controlled experiments, and
definite histopathological studies were also performed.
RESULTS
In vivo studies indicated statistically significant reduction in the incidence of
tumor formation with programmed and continuous AS intralesional treatment. For
established prostate cancer, AS treatment also demonstrated an inhibitory effect of
tumor growth compared with control. Histomorphological and immunohistochemical
studies demonstrated marked apoptosis after 5 weeks-AS continuous treatment in
Experiment II.
CONCLUSIONS
AS had a definite antitumor activity to inhibit tumorigenesis and may
modulate tumor growth of prostate cancer in vivo. It is non-toxic, readily avaliable and
inexpensive. AS, in the future, may be developed as a novel and effective treatment
in chemoprevention for human prostate cancer.