Skip Navigation


Carcinogenesis Advance Access originally published online on April 14, 2005
Carcinogenesis 2005 26(8):1450-1456; doi:10.1093/carcin/bgi089
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
26/8/1450    most recent
bgi089v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (31)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Volate, S. R.
Right arrow Articles by Wargovich, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Volate, S. R.
Right arrow Articles by Wargovich, M. J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Carcinogenesis vol.26 no.8 © Oxford University Press 2005; all rights reserved.

Modulation of aberrant crypt foci and apoptosis by dietary herbal supplements (quercetin, curcumin, silymarin, ginseng and rutin)

Suresh R. Volate, Destiny M. Davenport, Stephanie J. Muga and Michael J. Wargovich *

Division of Basic Research, South Carolina Cancer Center, 14 Medical Park, Suite 500 Columbia, SC 29203, USA

* To whom correspondence should be addressed. Tel: +1 803 434 4570; Fax: +1 803 434 3795; Email: michael.wargovich{at}palmettohealth.org

It is estimated that one-third of Americans use dietary herbal supplements on a regular basis. Diets rich in bioactive phytochemicals are associated with reduced risk of certain cancers, notably, colon cancer. Herbal supplements have not been directly tested as sources of bioactive cancer preventives. Hence, this study compares the ability of four herbal flavonoids (quercetin, curcumin, rutin and silymarin) and one whole herb mixture (ginseng powder) to suppress aberrant crypt foci (ACF) in an azoxymethane (AOM)-induced rat colon cancer model. Second, this study examines the effect of these herbal compounds on apoptosis and the mechanisms by which these compounds evoke apoptosis. The results of this study show that diets containing quercetin, curcumin, silymarin, ginseng and rutin decreased the number of ACFs by 4-, 2-, 1.8-, 1.5- and 1.2-fold, respectively compared with control. Histological analysis of the colon mucosa revealed that all the herbal supplements, except silymarin, induced apoptosis, with quercetin being the most potent (3x increase compared with control). Furthermore, ginseng and curcumin were region-specific in inducing apoptosis. The ability of quercetin and curcumin to modulate ACFs correlates well with their ability to induce apoptosis. Western blot analysis of caspase 9, Bax (proapoptotic) and Bcl-2 (antiapoptotic) proteins from the colon scraping suggests that quercetin and curcumin induce apoptosis via the mitochondrial pathway. Taken together, the results of this study suggest that these herbal supplements may exert significant and potentially beneficial effects on decreasing the amount of precancerous lesions and inducing apoptosis in the large intestine.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Cancer Epidemiol. Biomarkers Prev.Home page
G. Bobe, L. B. Sansbury, P. S. Albert, A. J. Cross, L. Kahle, J. Ashby, M. L. Slattery, B. Caan, E. Paskett, F. Iber, et al.
Dietary Flavonoids and Colorectal Adenoma Recurrence in the Polyp Prevention Trial
Cancer Epidemiol. Biomarkers Prev., June 1, 2008; 17(6): 1344 - 1353.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
A. Y. Issa, S. R. Volate, S. J. Muga, D. Nitcheva, T. Smith, and M. J. Wargovich
Green tea selectively targets initial stages of intestinal carcinogenesis in the AOM-ApcMin mouse model
Carcinogenesis, September 1, 2007; 28(9): 1978 - 1984.
[Abstract] [Full Text] [PDF]


Home page
Integr Cancer TherHome page
M. C. Comelli, U. Mengs, C. Schneider, and M. Prosdocimi
Toward the Definition of the Mechanism of Action of Silymarin: Activities Related to Cellular Protection From Toxic Damage Induced by Chemotherapy
Integr Cancer Ther, June 1, 2007; 6(2): 120 - 129.
[Abstract] [PDF]


Home page
Integr Cancer TherHome page
G. Deep and R. Agarwal
Chemopreventive Efficacy of Silymarin in Skin and Prostate Cancer
Integr Cancer Ther, June 1, 2007; 6(2): 130 - 145.
[Abstract] [PDF]


Home page
Cancer Epidemiol. Biomarkers Prev.Home page
E. Theodoratou, J. Kyle, R. Cetnarskyj, S. M. Farrington, A. Tenesa, R. Barnetson, M. Porteous, M. Dunlop, and H. Campbell
Dietary Flavonoids and the Risk of Colorectal Cancer
Cancer Epidemiol. Biomarkers Prev., April 1, 2007; 16(4): 684 - 693.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
L. J. Hofseth and M. J. Wargovich
Inflammation, Cancer, and Targets of Ginseng
J. Nutr., January 1, 2007; 137(1): 183S - 185S.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
C. C. Neto
Cranberry and Its Phytochemicals: A Review of In Vitro Anticancer Studies
J. Nutr., January 1, 2007; 137(1): 186S - 193S.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
C. Hoh, D. Boocock, T. Marczylo, R. Singh, D. P. Berry, A. R. Dennison, D. Hemingway, A. Miller, K. West, S. Euden, et al.
Pilot Study of Oral Silibinin, a Putative Chemopreventive Agent, in Colorectal Cancer Patients: Silibinin Levels in Plasma, Colorectum, and Liver and Their Pharmacodynamic Consequences.
Clin. Cancer Res., May 1, 2006; 12(9): 2944 - 2950.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.