Bile acids as endogenous etiologic agents in gastrointestinal cancer

被引:235
作者
Bernstein, Harris [1 ,2 ]
Bernstein, Carol [1 ,3 ]
Payne, Claire M. [1 ,2 ]
Dvorak, Katerina [1 ,2 ,3 ]
机构
[1] Univ Arizona, Coll Med, Dept Cell Biol & Anat, Tucson, AZ 85724 USA
[2] Univ Arizona, Arizona Canc Ctr, Tucson, AZ 85724 USA
[3] So Arizona Vet Affairs Hlth Care Syst, Tucson, AZ 85723 USA
关键词
Bile acids; Cancer; Adenocarcinoma; Esophagus; Stomach; Small intestine; Pancreas; Colon; Apoptosis; DNA damage; SALT-INDUCED APOPTOSIS; COLON EPITHELIAL-CELLS; NF-KAPPA-B; MULTIPLE STRESS-INDUCER; LARGE-BOWEL CANCER; CHAIN FATTY-ACIDS; DNA-DAMAGE; DEOXYCHOLIC-ACID; OXIDATIVE STRESS; COLORECTAL-CANCER;
D O I
10.3748/wjg.15.3329
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Bile acids are implicated as etiologic agents in cancer of the gastrointestinal (GI) tract, including cancer of the esophagus, stomach, small intestine, liver, biliary tract, pancreas and colon/rectum. Deleterious effects of bile acid exposure, likely related to carcinogenesis, include: induction of reactive oxygen and reactive nitrogen species; induction of DNA damage; stimulation of mutation; induction of apoptosis in the short term, and selection for apoptosis resistance in the long term. These deleterious effects have, so far, been reported most consistently in relation to esophageal and colorectal cancer, but also to some extent in relation to cancer of other organs. In addition, evidence is reviewed for an association of increased bile acid exposure with cancer risk in human populations, in specific human genetic conditions, and in animal experiments. A model for the role of bile acids in GI carcinogenesis is presented from a Darwinian perspective that offers an explanation for how the observed effects of bile acids on cells contribute to cancer development. (C) 2009 The WJG Press and Baishideng. All rights reserved.
引用
收藏
页码:3329 / 3340
页数:12
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