Lung cancer is the most common cause of cancer deaths worldwide, with one of every three cancer-related deaths attributable to lung cancer. As most current and former smokers have small (< 2 mm) nodules, a sound chemoprevention strategy would be to prevent their further growth by targeting angiogenesis. Consequently, mechanism-based angioprevention approaches employing animal models are realistic strategies to develop tools for combating lung cancer. Completed studies by us show that feeding silibinin, the major active constituent in milk thistle extract, a widely consumed dietary supplement, to A/J mice results in a 38-46% inhibition in lung tumor number and up to 93% inhibition of urethane-induced lung tumor growth. Immunohistochemical (IHC) analyses of the lung tumors showed strong inhibition of CD31 and iNOS staining in silibinin fed compared to urethane alone mice. Based on these studies and the fact that iNOS plays an important role in both angiogenic and extra-angiogenic (e.g. proliferation and apoptosis) mechanisms, we hypothesize that silibinin is a novel non-toxic agent that targets iNOS regulation in its angiopreventive efficacy against lung tumorigenesis. To test this hypothesis, our specific aims are: 1) To further assess and establish iNOS regulation and angioprevention in silibinin efficacy against urethane-induced lung tumorigenesis, 2) To assess and establish whether iNOS is the sole target of silibinin's mechanism of ameliorating mouse lung tumorigenesis, or whether an alternate/additional pathway also exists, 3) To identify and define the mechanisms by which silibinin modulates iNOS levels in lung cancer cells, and to establish the in vivo significance of these mechanisms in the overall anti-tumor efficacy of silibinin, and 4) To identify and define the role of iNOS regulation by silibinin in its overall angiopreventive efficacy, employing endothelial and lung cancer cell cultures. We anticipate that these proposed studies, together with our earlier work, will identify silibinin as a mechanism-based agent for the prevention and growth control of lung cancer. This will establish its in vivo efficacy in pre-clinical carcinogenic and genetic models. As a practical and translational approach, the long range goal of these studies is to define and establish the usefulness of silibinin for preventing and controlling human lung cancer growth. Accordingly, completion of the studies proposed in this grant would position us for a pilot clinical trial with silibinin in lung cancer patients and in those suspected of being at high risk for lung cancer development.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA113876-04
Application #
7367838
Study Section
Special Emphasis Panel (ZRG1-ONC-B (05))
Program Officer
Perloff, Marjorie
Project Start
2005-04-01
Project End
2010-02-28
Budget Start
2008-03-01
Budget End
2009-02-28
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
Mateen, Samiha; Raina, Komal; Agarwal, Rajesh (2013) Chemopreventive and anti-cancer efficacy of silibinin against growth and progression of lung cancer. Nutr Cancer 65 Suppl 1:3-11
Mateen, Samiha; Raina, Komal; Agarwal, Chapla et al. (2013) Silibinin synergizes with histone deacetylase and DNA methyltransferase inhibitors in upregulating E-cadherin expression together with inhibition of migration and invasion of human non-small cell lung cancer cells. J Pharmacol Exp Ther 345:206-14
Tyagi, Alpna; Agarwal, Chapla; Dwyer-Nield, Lori D et al. (2012) Silibinin modulates TNF-? and IFN-? mediated signaling to regulate COX2 and iNOS expression in tumorigenic mouse lung epithelial LM2 cells. Mol Carcinog 51:832-42
Mateen, Samiha; Raina, Komal; Jain, Anil K et al. (2012) Epigenetic modifications and p21-cyclin B1 nexus in anticancer effect of histone deacetylase inhibitors in combination with silibinin on non-small cell lung cancer cells. Epigenetics 7:1161-72
Ramasamy, Kumaraguruparan; Dwyer-Nield, Lori D; Serkova, Natalie J et al. (2011) Silibinin prevents lung tumorigenesis in wild-type but not in iNOS-/- mice: potential of real-time micro-CT in lung cancer chemoprevention studies. Clin Cancer Res 17:753-61
Ravichandran, Kameswaran; Tyagi, Alpna; Deep, Gagan et al. (2011) Interleukin-1beta-induced iNOS expression in human lung carcinoma A549 cells: involvement of STAT and MAPK pathways. Indian J Exp Biol 49:840-7
Redente, Elizabeth F; Dwyer-Nield, Lori D; Merrick, Daniel T et al. (2010) Tumor progression stage and anatomical site regulate tumor-associated macrophage and bone marrow-derived monocyte polarization. Am J Pathol 176:2972-85
Mateen, Samiha; Tyagi, Alpna; Agarwal, Chapla et al. (2010) Silibinin inhibits human nonsmall cell lung cancer cell growth through cell-cycle arrest by modulating expression and function of key cell-cycle regulators. Mol Carcinog 49:247-58
Tyagi, Alpna; Singh, Rana P; Ramasamy, Kumaraguruparan et al. (2009) Growth inhibition and regression of lung tumors by silibinin: modulation of angiogenesis by macrophage-associated cytokines and nuclear factor-kappaB and signal transducers and activators of transcription 3. Cancer Prev Res (Phila) 2:74-83
Singh, Rana P; Agarwal, Rajesh (2009) Cosmeceuticals and silibinin. Clin Dermatol 27:479-84

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