The Wnt Signaling Pathway Effector TCF7L2 and Type 2 Diabetes Mellitus

被引:148
作者
Jin, Tianru
Liu, Ling
机构
[1] Univ Toronto, Dept Med, Toronto, ON M5S 1A1, Canada
[2] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A1, Canada
[3] Univ Toronto, Lab Med & Pathobiol, Toronto, ON M5S 1A1, Canada
[4] Univ Hlth Network, Toronto Gen Res Inst, Div Cell & Mol Biol, Toronto, ON M5G 1L7, Canada
关键词
D O I
10.1210/me.2008-0135
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Since the relationship between TCF7L2 (also known as TCF-4) polymorphisms and type 2 diabetes mellitus was identified in 2006, extensive genome-wide association examinations in different ethnic groups have further confirmed this relationship. As a component of the bipartite transcription factor beta-catenin/TCF, TCF7L2 is important in conveying Wnt signaling during embryonic development and in regulating gene expression during adulthood. Although we still do not know mechanistically how the polymorphisms within the intron regions of TCF7L2 affect the risk of type 2 diabetes, this transcriptional regulator was shown to be involved in stimulating the proliferation of pancreatic beta-cells and the production of the incretin hormone glucagon-like peptide-1 in intestinal endocrine L cells. In this review, we introduce background knowledge of TCF7L2 as a component of the Wnt signaling pathway, summarize recent findings demonstrating the association between TCF7L2 polymorphisms and the risk of type 2 diabetes, outline experimental evidence of the potential function of TCF7L2 in pancreatic and intestinal endocrine cells, and present our perspective views. (Molecular Endocrinology 22: 2383-2392, 2008)
引用
收藏
页码:2383 / 2392
页数:10
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