4.5 Article

RUNX3 inhibits survivin expression and induces cell apoptosis in gastric cancer

期刊

EUROPEAN JOURNAL OF CELL BIOLOGY
卷 93, 期 3, 页码 118-126

出版社

ELSEVIER GMBH, URBAN & FISCHER VERLAG
DOI: 10.1016/j.ejcb.2014.02.002

关键词

Gastric cancer; RUNX3; Survivin; Cell apoptosis

资金

  1. National Natural Science Foundation of China [30800406, 81171536, 81371781, 81201935, 30972775, 30971151]
  2. National Basic Research Program of China (973 Program) [2012CB911202]
  3. Science Foundation of Shandong Province [BS2010YY040, ZR2009CZ001, ZR2009CM002]
  4. Medicine and Health Care in Shandong Province Science and Technology Development Plan [2013WS0205]
  5. Independent Innovative Foundation of Shandong University [2012TS126]

向作者/读者索取更多资源

Transcription factor RUNX3 is associated with gastric tumorigenesis and progression through regulating the expression of its target genes. Survivin is a member of the inhibitor of apoptosis (IAP)family and has been shown to inhibit cell apoptosis and promote cell proliferation. Increased survivin expression has been found in various cancer types, including gastric cancer. In this study, we found that restoration of RUNX3 promotes cell apoptosis through inhibiting the survivin expression, while RUNX3 inhibition increases the expression of survivin in gastric cancer cell lines. Moreover, RUNX3 over-expression inhibits,whereas its inhibition increases, the promoter activity of survivin gene, respectively. RUNX3-R122C, a mutation located in the conserved Runt domain, has no effect on the promoter activity of survivin gene. We further identified a RUNX3-binding site in the promoter of survivin gene and the binding of RUNX3 on survivin promoter leads to significantly inhibition of survivin expression. Finally, we confirmed the negative correlation of RUNX3 and survivin expression in clinical specimens of gastric cancer. These findings reveal a novel mechanism of RUNX3 for the induction of cell apoptosis in human gastric cancer. (C) 2014 Elsevier GmbH. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据