Deoxycholate induces mitochondrial oxidative stress and activates NF-κB through multiple mechanisms in HCT-116 colon epithelial cells

被引:141
作者
Payne, C. M. [1 ]
Weber, C.
Crowley-Skillicorn, C.
Dvorak, K.
Bernstein, H.
Bernstein, C.
Holubec, H.
Dvorakova, B.
Garewal, H.
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] Univ Arizona, Coll Med, Dept Internal Med, Tucson, AZ 85724 USA
[4] So Arizona Vet Affairs Hlth Care Syst, Tucson, AZ USA
关键词
D O I
10.1093/carcin/bgl139
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nuclear factor kappa B (NF-kappa B) is a redox-associated transcription factor that is involved in the activation of survival pathways. We have previously shown that deoxycholate (DOC) activates NF-kappa B in hepatocytes and colon epithelial cells and that persistent exposure of HCT-116 cells to increasing concentrations of DOC results in the constitutive activation of NF-kappa B, which is associated with the development of apoptosis resistance. The mechanisms by which DOC activates NF-kappa B in colon epithelial cells, and whether natural antioxidants can reduce DOC-induced NF-kappa B activation, however, are not known. Also, it is not known if DOC can generate reactive oxygen species within mitochondria as a possible pathway of stress-related NF-kappa B activation. Since we have previously shown that DOC activates the NF-kappa B stress-response pathway in HCT-116 cells, we used this cell line to further explore the mechanisms of NF-kappa B activation. We found that DOC induces mitochondrial oxidative stress and activates NF-kappa B in HCT-116 cells through multiple mechanisms involving NAD(P)H oxidase, Na+/K+-ATPase, cytochrome P450, Ca++ and the terminal mitochondrial respiratory complex IV. DOC-induced NF-kappa B activation was significantly (P < 0.05) inhibited by pre-treatment of cells with CAPE, EGCG, TMS, DPI, NaN3, EGTA, Ouabain and RuR. The NF-kappa B-activating pathways, induced by the dietary-related endogenous detergent DOC, provide mechanisms for promotion of colon cancer and identify possible new targets for chemoprevention.
引用
收藏
页码:215 / 222
页数:8
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