Chemoprotective effects of curcumin in esophageal epithelial cells exposed to bile acids

被引:36
作者
Bower, Matthew R. [1 ,2 ]
Aiyer, Harini S. [1 ,2 ]
Li, Yan [1 ,2 ]
Martin, Robert C. G. [1 ,2 ]
机构
[1] Univ Louisville, Sch Med, Div Surg Oncol, Dept Surg, Louisville, KY 40202 USA
[2] Univ Louisville, Sch Med, James Graham Brown Canc Ctr, Louisville, KY 40202 USA
基金
美国国家卫生研究院;
关键词
Esophageal cancer; Curcumin; Cyclooxygenase-2; Superoxide dismutase; Chemoprevention; SUPEROXIDE-DISMUTASE EXPRESSION; GASTROESOPHAGEAL-REFLUX DISEASE; CHEMOPREVENTIVE AGENT CURCUMIN; I CLINICAL-TRIAL; NF-KAPPA-B; BARRETTS-ESOPHAGUS; OXIDATIVE STRESS; FREE-RADICALS; DEOXYCHOLIC-ACID; CANCER;
D O I
10.3748/wjg.v16.i33.4152
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To investigate the ability of curcumin to counteract the impact of bile acids on gene expression of esophageal epithelial cells. METHODS: An esophageal epithelial cell line (HET-1A) was treated with curcumin in the presence of deoxycholic acid. Cell proliferation and viability assays were used to establish an appropriate dose range for curcumin. The combined and individual effects of curcumin and bile acid on cyclooxygenase-2 (COX-2) and superoxide dismutase (SOD-1 and SOD-2) gene expression were also assessed. RESULTS: Curcumin in a dose range of 10-100 mu mol/L displayed minimal inhibition of HET-1A cell viability. Deoxycholic acid at a concentration of 200 mu mol/L caused a 2.4-fold increase in COX-2 gene expression compared to vehicle control. The increased expression of COX-2 induced by deoxycholic acid was partially reversed by the addition of curcumin, and curcumin reduced COX-2 expression 3.3- to 1.3-fold. HET-1A cells exposed to bile acid yielded reduced expression of SOD-1 and SOD-2 genes with the exception that high dose deoxycholic acid at 200 mu mol/L led to a 3-fold increase in SOD-2 expression. The addition of curcumin treatment partially reversed the bile acid-induced reduction in SOD-1 expression at all concentrations of curcumin tested. CONCLUSION: Curcumin reverses bile acid suppression of gene expression of SOD-1. Curcumin is also able to inhibit bile acid induction of COX-2 gene expression. (C) 2010 Baishideng. All rights reserved.
引用
收藏
页码:4152 / 4158
页数:7
相关论文
共 44 条
[1]
Aggarwal BB, 2003, ANTICANCER RES, V23, P363
[2]
Nicotinic receptors mediate tumorigenic action of tobacco-derived nitrosamines on immortalized oral epithelial cells [J].
Arredondo, Juan ;
Chernyavsky, Alex I. ;
Grando, Sergei A. .
CANCER BIOLOGY & THERAPY, 2006, 5 (05) :511-517
[3]
Effect of Chronic Intake of NSAIDs and Cyclooxygenase 2-Selective Inhibitors on Esophageal Cancer Incidence [J].
Bardou, Marc ;
Barkun, Alan N. ;
Ghosn, Joumana ;
Hudson, Marie ;
Rahme, Elham .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2004, 2 (10) :880-887
[4]
Bile acids as carcinogens in human gastrointestinal cancers [J].
Bernstein, H ;
Bernstein, C ;
Payne, CM ;
Dvorakova, K ;
Garewal, H .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2005, 589 (01) :47-65
[5]
Chemoprevention of esophageal adenocarcinoma by COX-2 inhibitors in an animal model of Barrett's esophagus [J].
Buttar, NS ;
Wang, KK ;
Leontovich, O ;
Westcott, JY ;
Pacifico, RJ ;
Anderson, MA ;
Krishnadath, KK ;
Lutzke, LS ;
Burgart, LJ .
GASTROENTEROLOGY, 2002, 122 (04) :1101-1112
[6]
Cheng AL, 2001, ANTICANCER RES, V21, P2895
[7]
Phase II trial of curcumin in patients with advanced pancreatic cancer [J].
Dhillon, Navneet ;
Aggarwal, Bharat B. ;
Newman, Robert A. ;
Wolff, Robert A. ;
Kunnumakkara, Ajaikumar B. ;
Abbruzzese, James L. ;
Ng, Chaan S. ;
Badmaev, Vladimir ;
Kurzrock, Razelle .
CLINICAL CANCER RESEARCH, 2008, 14 (14) :4491-4499
[8]
Esophageal acid exposure at pH ≤ 2 is more common in Barrett's esophagus patients and is associated with oxidative stress [J].
Dvorak, K. ;
Fass, R. ;
Dekel, R. ;
Payne, C. M. ;
Chavarria, M. ;
Dvorakova, B. ;
Bernstein, H. ;
Bernstein, C. ;
Garewal, H. .
DISEASES OF THE ESOPHAGUS, 2006, 19 (05) :366-372
[9]
Bile acids in combination with low pH induce oxidative stress and oxidative DNA damage: relevance to the pathogenesis of Barrett's oesophagus [J].
Dvorak, Katerina ;
Payne, Claire M. ;
Chavarria, Melissa ;
Ramsey, Lois ;
Dvorakova, Barbora ;
Bernstein, Harris ;
Holubec, Hana ;
Sampliner, Richard E. ;
Guy, Naihsuan ;
Condon, Amanda ;
Bernstein, Carol ;
Green, Sylvan B. ;
Prasad, Anil ;
Garewal, Harinder S. .
GUT, 2007, 56 (06) :763-771
[10]
Epidemiology and pathogenesis of esophageal cancer [J].
Holmes, Rebecca S. ;
Vaughan, Thomas L. .
SEMINARS IN RADIATION ONCOLOGY, 2007, 17 (01) :2-9