How does the human RUNX3 gene induce apoptosis in gastric cancer? Latest data, reflections and reactions

被引:58
作者
Vogiatzi, Paraskevi
De Falco, Giulia
Claudio, Pier Paolo
Giordano, Antonio
机构
[1] Temple Univ, Coll Sci & Technol, Sbarro Inst Canc Res & Mol Med, Philadelphia, PA 19122 USA
[2] Univ Siena, Dept Human Pathol & Oncol, I-53100 Siena, Italy
[3] Univ Siena, Dept Mol Biol, Med Genet Unit, I-53100 Siena, Italy
关键词
runt-related (RUNX); RUNX3; FoxO3a/FKHRL1; tumor suppressor; gastric cancer;
D O I
10.4161/cbt.5.4.2748
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
RUNX3 is the oldest known gene in the RUNX family. Data have demonstrated its function to be thoroughly involved the neurogenesis of the dorsal root ganglia, T-cell differentiation and tumorigenesis of gastric epithelium. As a TGF-beta target, RUNX3 protein is believed to be involved in TGF-beta-mediated tumor suppressor pathway; however, little is known about its role in apoptosis. According to recent data reported by Yamamura et al., (J Biol Chem 2006; 281:5267-76), RUNX3 interacts with FoxO3a/FKHRL1 expressed in gastric cancer cells to activate Bim and induce apoptosis. The cooperation between RUNX3 and the PI3K/Akt signaling pathway component FoxO3a/FKHRL1 suggests the putative role of RUNX3 in the homoeostasis of gastric cells and in stomach cancer control. Here we discuss recent breakthroughs in our understanding of the mechanisms of RUNX3 in gastric malignancy and comment on possible future trends and perspectives.
引用
收藏
页码:371 / 374
页数:4
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