3¡¬-Hydroxypterostilbene Suppresses Colitis-Associated Tumorigenesis by Inhibition of IL-6/STAT3 Signaling in Mice
Journal
Journal of Agricultural and Food Chemistry
Journal Volume
65
Journal Issue
44
Pages
9655-9664
Date Issued
2017
Author(s)
Abstract
3¡¬-Hydroxypterostilbene (trans-3,5-dimethoxy-3¡¬,4¡¬-hydroxystilbene) presents in Sphaerophysa salsula, Pterocarpus marsupium, and honey bee propolis and has been reported to exhibit several biological activities. Herein, we aimed to explore the chemopreventive effects of dietary 3¡¬-hydroxypterostilbene and underlying molecular mechanisms on colitis-associated cancer using the azoxymethane (AOM)/dextran sodium sulfate (DSS) model. 3¡¬-Hydroxypterostilbene administration effectively ameliorated the colon shortening and number of tumors in AOM/DSS-treated mice (3.2 ¡Ó 1.2 of the high-dose treatment versus 13.8 ¡Ó 5.3 of the AOM/DSS group, p < 0.05). Molecular analysis exhibited the anti-inflammatory activity of 3¡¬-hydroxypterostilbene by a significant decrease in the levels of inducible nitric oxide synthase, cyclooxygenase-2, and interleukin-6 (IL-6) (p < 0.05). Moreover, dietary 3¡¬-hydroxypterostilbene also significantly diminished IL-6/signal transducer and activator of transcription signaling and restored colonic suppressor of cytokine signaling 3 levels in the colonic tissue of mice (p < 0.05). Collectively, these results demonstrated for the first time the in vivo chemopreventive efficacy and molecular mechanisms of dietary 3¡¬-hydroxypterostilbene against colitis-associated colonic tumorigenesis. ? 2017 American Chemical Society.
Subjects
3¡¬-hydroxypterostilbene
azoxymethane
colitis
dextran sodium sulfate
inflammation
SDGs
Other Subjects
Immunology; Mammals; Nitric oxide; Sodium; Sodium sulfate; Sulfur compounds; Anti-inflammatory activity; azoxymethane; Chemopreventive effects; colitis; High-dose treatment; Inducible nitric oxide synthase; inflammation; Suppressor of cytokine signaling 3; Diseases; 3'-hydroxypterostilbene; antineoplastic agent; cyclooxygenase 2; interleukin 6; STAT3 protein; stilbene derivative; animal; carcinogenesis; colitis; colon tumor; complication; disease model; drug effects; genetics; human; Institute for Cancer Research mouse; male; metabolism; mouse; signal transduction; Animals; Anticarcinogenic Agents; Carcinogenesis; Colitis; Colonic Neoplasms; Cyclooxygenase 2; Disease Models, Animal; Humans; Interleukin-6; Male; Mice; Mice, Inbred ICR; Signal Transduction; STAT3 Transcription Factor; Stilbenes
Type
journal article