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  4. Prevention of colitis and colitis-associated colorectal cancer by a novel polypharmacological histone deacetylase inhibitor
 
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Prevention of colitis and colitis-associated colorectal cancer by a novel polypharmacological histone deacetylase inhibitor

Journal
Clinical Cancer Research
Journal Volume
22
Journal Issue
16
Pages
4158-4169
Date Issued
2016
Author(s)
TZU-TANG WEI  
Lin, Y.-T.
Tseng, R.-Y.
CHIA-TUNG SHUN  
Lin, Y.-C.
MING-SHIANG WU  
Fang, J.-M.  
CHING-CHOW CHEN  
DOI
10.1158/1078-0432.CCR-15-2379
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84982153314&doi=10.1158%2f1078-0432.CCR-15-2379&partnerID=40&md5=7f9de11cd2f5ec2a2527ef6362498e56
https://scholars.lib.ntu.edu.tw/handle/123456789/618283
Abstract
PURPOSE: Colorectal cancer is a worldwide cancer with rising annual incidence. Inflammation is a well-known cause of colorectal cancer carcinogenesis. Metabolic inflammation (metaflammation) and altered gut microbiota (dysbiosis) have contributed to colorectal cancer. Chemoprevention is an important strategy to reduce cancer-related mortality. Recently, various polypharmacologic molecules that dually inhibit histone deacetylases (HDAC) and other therapeutic targets have been developed. EXPERIMENTAL DESIGN: Prevention for colitis was examined by dextran sodium sulfate (DSS) mouse models. Prevention for colorectal cancer was examined by azoxymethane/dextran sodium sulfate (AOM/DSS) mouse models. Immunohistochemical staining was utilized to analyze the infiltration of macrophages and neutrophils and COX-II expression in mouse tissue specimens. The endotoxin activity was evaluated by Endotoxin Activity Assay Kit. RESULTS: We synthesized a statin hydroxamate that simultaneously inhibited HDAC and 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR). Its preventive effect on colitis and colitis-associated colorectal cancer in mouse models was examined. Oral administration of this statin hydroxamate could prevent acute inflammation in the DSS-induced colitis and AOM/DSS-induced colorectal cancer with superior activity than the combination of lovastatin and SAHA. It also reduced proinflammatory cytokines, chemokines, expression of COX-II, and cyclin D1 in inflammation and tumor tissues, as well as decreasing the infiltration of macrophages and neutrophils in tumor-surrounding regions. Stemness of colorectal cancer and the release of endotoxin in AOM/DSS mouse models were also attenuated by this small molecule. CONCLUSIONS: This study demonstrates that the polypharmacological HDAC inhibitor has promising effect on the chemoprevention of colorectal cancer, and serum endotoxin level might serve as a potential biomarker for its chemoprevention. Clin Cancer Res; 22(16); 4158-69. ©2016 AACR.
SDGs

[SDGs]SDG3

Publisher
American Association for Cancer Research Inc.
Type
journal article

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