Colorectal cancer (CRC) is the second most common cause of cancer deaths in humans, and about 5% of the US population will develop CRC in their life times. Overall, CRC growth, progression, and metastasis involve a gradual accumulation of genetic and epigenetic changes over a period of years. One approach to control CRC growth and metastasis could be its prevention by phytochemicals, which inhibit one or more neoplastic events and reduce the risk of cancer. One such phytochemical is silibinin, the major active constituent in a widely consumed dietary supplement, milk thistle extract. It is noteworthy that silibinin is devoid of any toxicity in animal studies as well as in humans. In fact, it is clinically used as hepatoprotective agent in humans. Recently, we observed that silibinin significantly inhibits growth, causes G1/G2-M arrest, and induces apoptosis in human colon carcinoma HT29 cells, and that silibinin feeding significantly inhibits HT29 tumor xenograft growth in nude mice. Recent studies have also shown that silymarin (a crude form of silibinin) feeding prevents azoxymethane (AOM) and 1,2-dimethylhydrazine-induced colon carcinogenesis in rat model. Together, based on these studies, we hypothesize that silibinin is a novel colon cancer preventive agent, and targets cell cycle progression and cell survival signaling leading to its antiproliferative and apoptotic efficacy against CRC.
Our specific aims are to: I) further assess and establish silibinin efficacy in animal CRC models, II) define and establish molecular targets of silibinin effects on cell cycle progression, III) define effect of silibinin on cell survival/antiapoptotic signaling, and IV) examine and define effect of silibinin on apoptosis regulators. We anticipate that proposed studies, will identify silibinin as a mechanism-based agent for the prevention, growth control and therapy of CRC, and will establish its in vivo efficacy in pre-clinical carcinogenic, genetic and xenograft CRC models. As a practical and translational approach, the long-range goal of these studies would be to define and establish the usefulness of silibinin for the prevention and therapy of human CRC. Accordingly, we anticipate that completion of proposed studies in this grant would position us for a pilot clinical trial with silibinin in CRC patients.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA112304-04
Application #
7363662
Study Section
Special Emphasis Panel (ZRG1-ONC-B (02))
Program Officer
Malone, Winfred F
Project Start
2005-03-01
Project End
2010-01-31
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
4
Fiscal Year
2008
Total Cost
$288,389
Indirect Cost
Name
University of Colorado Denver
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Raina, Komal; Kumar, Sushil; Dhar, Deepanshi et al. (2016) Silibinin and colorectal cancer chemoprevention: a comprehensive review on mechanisms and efficacy. J Biomed Res 30:452-465
Derry, Molly M; Somasagara, Ranganatha R; Raina, Komal et al. (2014) Target identification of grape seed extract in colorectal cancer using drug affinity responsive target stability (DARTS) technique: role of endoplasmic reticulum stress response proteins. Curr Cancer Drug Targets 14:323-36
Kumar, Sushil; Raina, Komal; Agarwal, Chapla et al. (2014) Silibinin strongly inhibits the growth kinetics of colon cancer stem cell-enriched spheroids by modulating interleukin 4/6-mediated survival signals. Oncotarget 5:4972-89
Kumar, Sushil; Kumar, Dileep; Raina, Komal et al. (2014) Functional modification of adipocytes by grape seed extract impairs their pro-tumorigenic signaling on colon cancer stem cells and the daughter cancer cells. Oncotarget 5:10151-69
Derry, Molly M; Raina, Komal; Agarwal, Rajesh et al. (2014) Characterization of azoxymethane-induced colon tumor metastasis to lung in a mouse model relevant to human sporadic colorectal cancer and evaluation of grape seed extract efficacy. Exp Toxicol Pathol 66:235-42
Agarwal, Chapla; Wadhwa, Ritambhara; Deep, Gagan et al. (2013) Anti-cancer efficacy of silybin derivatives -- a structure-activity relationship. PLoS One 8:e60074
Agarwal, R; Kale, R K; Rao, C V et al. (2013) Introduction to Special Issue on Molecular Basis for Cancer Prevention with Bioactive Food Components in Nutrition and Cancer--an International Journal. Nutr Cancer 65 Suppl 1:1-2
Derry, Molly; Raina, Komal; Agarwal, Rajesh et al. (2013) Differential effects of grape seed extract against human colorectal cancer cell lines: the intricate role of death receptors and mitochondria. Cancer Lett 334:69-78
Raina, Komal; Agarwal, Chapla; Agarwal, Rajesh (2013) Effect of silibinin in human colorectal cancer cells: targeting the activation of NF-?B signaling. Mol Carcinog 52:195-206
Deep, Gagan; Agarwal, Rajesh (2013) Targeting tumor microenvironment with silibinin: promise and potential for a translational cancer chemopreventive strategy. Curr Cancer Drug Targets 13:486-99

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