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早期生长反应基因1(EGR1)调节肿瘤细胞中乙酰肝素酶基因的转录。

Early growth response gene 1 (EGR1) regulates heparanase gene transcription in tumor cells.

作者信息

de Mestre Amanda M, Rao Sudha, Hornby June R, Soe-Htwe Thura, Khachigian Levon M, Hulett Mark D

机构信息

Cancer and Vascular Biology Group, Division of Immunology and Genetics, The John Curtin School of Medical Research, The Australian National University, Acton ACT 2601.

出版信息

J Biol Chem. 2005 Oct 21;280(42):35136-47. doi: 10.1074/jbc.M503414200. Epub 2005 Aug 10.

Abstract

Heparanase is an endoglycosidase that degrades heparan sulfate chains of heparan sulfate proteoglycans, a key component of extracellular matrix and basement membranes. Studies using heparanase inhibitors and gene silencing have provided evidence to support an important role for heparanase in tumor metastasis and angiogenesis. The expression of heparanase is normally very tightly controlled, however, it is commonly deregulated in tumor cells, which express elevated heparanase activity that correlates with high levels of heparanase mRNA. We recently identified the transcription factor early growth response gene 1, EGR1, as a key regulator of inducible heparanase transcription in T cells. In this study using chromatin immunoprecipitation, we demonstrate for the first time that EGR1 binds to the heparanase gene promoter in vivo. The important question of the role of EGR1 in regulating heparanase transcription in tumor cells was then assessed. Studies were carried out in four epithelial tumor lines of different tissue origin. Functional dissection of the heparanase promoter identified a 280-bp region that was critical for transcription of the heparanase gene. Transactivation studies using an EGR1 expression vector co-transfected with a reporter construct containing the 280-bp region showed EGR1-activated heparanase promoter activity in a dose-dependent manner in prostate or breast adenocarcinoma and colon carcinoma cell lines. In contrast, overexpression of EGR1 resulted in a dose-dependent repression of promoter activity in melanoma cells. Using site-directed mutagenesis the 280-bp region was found to contain two functional EGR1 sites and electrophoretic mobility shift assays showed binding of EGR1 to both of these sites upon activation of tumor cells. Furthermore, the heparanase promoter region containing the EGR1 sites was also inducible in tumor cells and induction corresponded to HPSE expression levels. These studies show that EGR1 regulates heparanase transcription in tumor cells and importantly, can have a repressive or activating role depending on the tumor type.

摘要

乙酰肝素酶是一种内切糖苷酶,可降解硫酸乙酰肝素蛋白聚糖的硫酸乙酰肝素链,而硫酸乙酰肝素蛋白聚糖是细胞外基质和基底膜的关键组成部分。使用乙酰肝素酶抑制剂和基因沉默的研究提供了证据,支持乙酰肝素酶在肿瘤转移和血管生成中发挥重要作用。通常,乙酰肝素酶的表达受到非常严格的控制,然而,它在肿瘤细胞中常常失调,肿瘤细胞中乙酰肝素酶活性升高,且与高水平的乙酰肝素酶mRNA相关。我们最近鉴定出转录因子早期生长反应基因1(EGR1)是T细胞中诱导型乙酰肝素酶转录的关键调节因子。在这项使用染色质免疫沉淀的研究中,我们首次证明EGR1在体内与乙酰肝素酶基因启动子结合。随后评估了EGR1在调节肿瘤细胞中乙酰肝素酶转录方面作用的重要问题。在四种不同组织来源的上皮肿瘤细胞系中开展了研究。对乙酰肝素酶启动子进行功能剖析,确定了一个对乙酰肝素酶基因转录至关重要的280 bp区域。使用与包含280 bp区域的报告构建体共转染的EGR1表达载体进行的反式激活研究表明,在前列腺癌或乳腺癌以及结肠癌细胞系中,EGR1以剂量依赖的方式激活乙酰肝素酶启动子活性。相比之下,EGR1的过表达导致黑色素瘤细胞中启动子活性呈剂量依赖性抑制。使用定点诱变发现,280 bp区域包含两个功能性EGR1位点,电泳迁移率变动分析表明,肿瘤细胞激活后EGR1与这两个位点均结合。此外,包含EGR1位点的乙酰肝素酶启动子区域在肿瘤细胞中也可被诱导,且诱导作用与HPSE表达水平相对应。这些研究表明,EGR1调节肿瘤细胞中乙酰肝素酶的转录,重要的是,根据肿瘤类型,EGR1可发挥抑制或激活作用。

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