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LY294002通过诱导早期生长反应基因1抑制白血病细胞的侵袭和迁移,且不依赖磷脂酰肌醇3-激酶-Akt途径。

LY294002 inhibits leukemia cell invasion and migration through early growth response gene 1 induction independent of phosphatidylinositol 3-kinase-Akt pathway.

作者信息

Liu Peng, Xu Bei, Li Jianyong, Lu Hua

机构信息

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, People's Republic of China.

出版信息

Biochem Biophys Res Commun. 2008 Dec 5;377(1):187-90. doi: 10.1016/j.bbrc.2008.09.094. Epub 2008 Oct 1.

Abstract

LY294002 (LY29) is a commonly used pharmacologic inhibitor of the phosphatidylinositol 3-kinase (PI3K) and has shown antitumorigenic effect both in vivo and in vitro. Both LY29 and its inactive analogue, LY303511 (LY30), significantly up-regulated early growth response gene 1 (Egr-1) expression in HL-60 leukemic cells. However, wortmannin, another commonly used PI3K inhibitor, was not able to induce Egr-1 at the dose that completely blocked Akt phosphorylation. LY29 markedly decreased the invasive cells number through Matrigel and human umbilical vein endothelial cells (HUVECs) compared with the controls. Moreover, the inhibitory effects could be significantly abolished by Egr-1 gene silencing with siRNA technology. Our results indicated for the first time that LY29 could suppress leukemia cell invasion and migration at least in part through up-regulation of Egr-1, independent of its PI3K-Akt inhibitory activity. These data provide a novel explanation for the anticancer properties of LY29 in leukemias.

摘要

LY294002(LY29)是一种常用的磷脂酰肌醇3激酶(PI3K)药理学抑制剂,已在体内和体外显示出抗肿瘤作用。LY29及其无活性类似物LY303511(LY30)均能显著上调HL-60白血病细胞中早期生长反应基因1(Egr-1)的表达。然而,另一种常用的PI3K抑制剂渥曼青霉素在完全阻断Akt磷酸化的剂量下并不能诱导Egr-1。与对照组相比,LY29显著减少了通过基质胶和人脐静脉内皮细胞(HUVECs)的侵袭细胞数量。此外,利用小干扰RNA(siRNA)技术沉默Egr-1基因可显著消除这种抑制作用。我们的结果首次表明,LY29至少部分地通过上调Egr-1来抑制白血病细胞的侵袭和迁移,这与其PI3K-Akt抑制活性无关。这些数据为LY29在白血病中的抗癌特性提供了一种新的解释。

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