Garcinol suppresses inflammation-associated colon carcinogenesis in mice
Journal
Molecular Nutrition and Food Research
Journal Volume
58
Journal Issue
9
Pages
1820-1829
Date Issued
2014
Author(s)
Abstract
Scope: Garcinol is a polyisoprenylated benzophenone derivative isolated from the fruit rind of Garcinia indica and has exhibited chemopreventive effects on azoxymethane)-induced colonic aberrant crypt foci in mice. In this study, we investigated whether garcinol protects against dextran sulfate sodium (DSS) induced colitis/inflammation and azoxymethane/DSS-induced inflammation-related colon tumorigenesis in male ICR mice. We also aimed to delineate the possible molecular mechanisms responsible for these effects. Methods and results: Treatment with garcinol prevented shortening of the colon length and the formation of aberrant crypt foci and improved the inflammation score in the mouse colon stimulated by DSS. Moreover, administration of garcinol markedly decreased DSS-induced inducible nitric oxide synthase, cyclooxygenase-2, and proliferating cell nuclear antigen protein expression. The dietary administration of garcinol effectively reduced the tumor size and incidence in the mouse colon. Western blot and immunohistochemical analysis revealed that administration of garcinol significantly downregulated cyclooxygenase-2, cyclin D1, and vascular endothelial growth factor expression via inhibition of the extracellular signal-regulated protein kinase 1/2, phosphatidylinositol 3 kinase/Akt/p70 ribosomal S6 kinase, and Wnt/β-catenin signaling pathways. Conclusion: Our results suggest that garcinol may merit further clinical investigation as a chemoprophylactic food that helps prevent colitis-associated colon cancer. ? 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Subjects
Azoxymethane/Dextran sulfate sodium; Chemopreventive; Colon carcinogenesis; Garcinol; Inflammation
SDGs
Other Subjects
Mus; antineoplastic agent; autacoid; azoxymethane; beta catenin; dextran sulfate; garcinol; terpene; animal; chemically induced; colitis; Colonic Neoplasms; complication; drug effects; hepatitis; Institute for Cancer Research mouse; lipid metabolism; male; metabolism; Neoplasms, Experimental; pathology; signal transduction; Animals; Anticarcinogenic Agents; Azoxymethane; beta Catenin; Colitis; Colonic Neoplasms; Dextran Sulfate; Hepatitis; Inflammation Mediators; Lipid Metabolism; Male; Mice, Inbred ICR; Neoplasms, Experimental; Signal Transduction; Terpenes
Type
journal article