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PMID: 16093249 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

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

The Journal of biological chemistry ·Vol. 280 ·No. 42 ·2005-10-21 ·Pages 35136-47

de Mestre AM, Rao S, Hornby JR, Soe-Htwe T, Khachigian LM, Hulett MD

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.

MeSH Terms
Animals Base Sequence Binding Sites Blotting, Western Cell Line Cell Line, Tumor Cell Nucleus/metabolism Chromatin Immunoprecipitation DNA Primers/chemistry Dose-Response Relationship, Drug Early Growth Response Protein 1/metabolism,physiology Genes, Reporter Glucuronidase/biosynthesis,genetics,metabolism Heparan Sulfate Proteoglycans/chemistry Humans Jurkat Cells Luciferases/metabolism Melanoma/metabolism Mice Molecular Sequence Data Mutagenesis, Site-Directed Neoplasms/metabolism Neovascularization, Pathologic Plasmids/metabolism Promoter Regions, Genetic RNA/metabolism RNA, Messenger/metabolism Reverse Transcriptase Polymerase Chain Reaction Transcription, Genetic Transcriptional Activation Transfection
Chemicals
DNA Primers EGR1 protein, human Early Growth Response Protein 1 Heparan Sulfate Proteoglycans RNA, Messenger RNA Luciferases heparanase Glucuronidase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
de Mestre Amanda M
Cancer and Vascular Biology Group, Division of Immunology and Genetics, The John Curtin School of Medical Research, The Australian National University, Acton ACT 2601.
Rao Sudha
Hornby June R
Soe-Htwe Thura
Khachigian Levon M
Hulett Mark D
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2005-10-21
Epub
2005-00-10
Pages
35136-47
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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