SLC5A8 (SMCT1)-mediated transport of butyrate forms the basis for the tumor suppressive function of the transporter

被引:164
作者
Gupta, N
Martin, PM
Prasad, PD
Ganapathy, V [1 ]
机构
[1] Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
[2] Med Coll Georgia, Dept Surg, Augusta, GA 30912 USA
[3] Med Coll Georgia, Dept Obstet & Gynecol, Augusta, GA 30912 USA
关键词
SLC5A8; butyrate; historic deacetylases; colon cancer; colonic bacteria; dietary fiber; short-chain fatty acids;
D O I
10.1016/j.lfs.2005.10.028
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The identification of SLC5A8 as a tumor suppressor gene in colorectal cancer marks, for the first time, the association of a plasma membrane transporter with tumor suppressive properties. The subsequent establishment of the functional identity of SLC5A8 as a Na+-coupled transporter for short-chain monocarboxylates provides a mechanism for the turner suppressive function of the transporter. Butyrate, a substrate for the transporter, is a historic deacetylase inhibitor and protective against colorectal cancer. This fatty acid is produced in the colonic lumen by bacterial fermentation of dietary fiber. SLC5A8 mediates the concentrative entry of butyrate from die lumen into colonocytes. Consequently, the transport function of SLC5A8 has the ability to influence the acetylation status of histories and hence gene expression in colonocytes. The ability of SLC5A8 to deliver butyrate into colonic epithelial cells most likely underlies the tumor suppressive role of this transporter. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:2419 / 2425
页数:7
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