Department of Biological Sciences, College of Natural Sciences, University of Ulsan, Ulsan, 44610, South Korea.
Division of Life Sciences, College of Life Sciences and Bioengineering, Incheon National University, Incheon, 22012, South Korea.
Biochem Biophys Res Commun. 2019 Apr 2;511(2):398-403. doi: 10.1016/j.bbrc.2019.02.069. Epub 2019 Feb 21.
Here, we report that Forkhead Box O1 (FOXO1) protein, a tumor suppressor, regulates expression of nicotinamide phosphoribosyltransferase (Nampt) in human breast cancer MCF-7 cells. Nampt plays an important role in the regulation of cell growth, survival, DNA replication and repair, and angiogenesis in tumorigenesis. We revealed that FOXO1 directly inhibits Nampt expression via binding to FOXO1 binding domains in the 5'-flanking region of the nampt gene. Nampt expression was increased by insulin and downstream phosphatidylinositol 3-kinase (PI3K)/Akt signaling, which was inhibited by FOXO1 overexpression. Accordingly, we showed that FOXO1 is also involved in insulin signaling-induced cell survival and proliferation in MCF-7 cells. These results suggest that FOXO1 plays an important role in human breast cancer cells by regulating nampt gene expression.
在这里,我们报告叉头框蛋白 O1(FOXO1)蛋白作为一种肿瘤抑制因子,调节人乳腺癌 MCF-7 细胞中烟酰胺磷酸核糖转移酶(Nampt)的表达。Nampt 在肿瘤发生过程中细胞生长、存活、DNA 复制和修复以及血管生成的调控中发挥重要作用。我们揭示了 FOXO1 通过与 nampt 基因 5'侧翼区域的 FOXO1 结合域直接抑制 Nampt 的表达。胰岛素和下游磷脂酰肌醇 3-激酶(PI3K)/Akt 信号通路增加 Nampt 的表达,而过表达 FOXO1 则抑制其表达。因此,我们表明 FOXO1 还参与 MCF-7 细胞中胰岛素信号诱导的细胞存活和增殖。这些结果表明,FOXO1 通过调节 nampt 基因的表达,在人类乳腺癌细胞中发挥重要作用。