Gut Microbiota Imbalance and Base Excision Repair Dynamics in Colon Cancer

被引:28
作者
Ray, Debolina [1 ]
Kidane, Dawit [1 ]
机构
[1] Univ Texas Austin, Dell Pediat Res Inst, Div Pharmacol & Toxicol, Coll Pharm, 1400 Barbara Jordan Blvd,R1800,Mail Code R1800, Austin, TX 78723 USA
来源
JOURNAL OF CANCER | 2016年 / 7卷 / 11期
基金
美国国家卫生研究院;
关键词
Microbiota; Base excision repair; Colon cancer; DNA-POLYMERASE-BETA; CYTOLETHAL DISTENDING TOXIN; GASTRIC EPITHELIAL-CELLS; COLORECTAL-CANCER; HELICOBACTER-PYLORI; GENOMIC INSTABILITY; MISMATCH REPAIR; OXIDIZED BASES; O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE; ENHANCED EXPRESSION;
D O I
10.7150/jca.15480
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gut microbiota are required for host nutrition, energy balance, and regulating immune homeostasis, however, in some cases, this mutually beneficial relationship becomes twisted (dysbiosis), and the gut flora can incite pathological disorders including colon cancer. Microbial dysbiosis promotes the release of bacterial genotoxins, metabolites, and causes chronic inflammation, which promote oxidative DNA damage. Oxidized DNA base lesions are removed by base excision repair (BER), however, the role of this altered function of BER, as well as microbiota-mediated genomic instability and colon cancer development, is still poorly understood. In this review article, we will discuss how dysbiotic microbiota induce DNA damage, its impact on base excision repair capacity, the potential link of host BER gene polymorphism, and the risk of dysbiotic microbiota mediated genomic instability and colon cancer.
引用
收藏
页码:1421 / 1430
页数:10
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