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

被引:72
作者
de Mestre, AM
Rao, S
Hornby, JR
Soe-Htwe, T
Khachigian, LM
Hulett, MD [1 ]
机构
[1] Australian Natl Univ, John Curtin Sch Med Res, Div Immunol & Genet, Canc & Vasc Biol Grp, Acton, ACT 2601, Australia
[2] Univ New S Wales, Ctr Vasc Res, Sydney, NSW 2052, Australia
关键词
D O I
10.1074/jbc.M503414200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:35136 / 35147
页数:12
相关论文
共 69 条
  • [31] Cloning and characterization of the human heparanase-1 (HPR1) gene promoter -: Role of GA-binding protein and Sp1 in regulating HPR1 basal promoter activity
    Jiang, P
    Kumar, A
    Parrillo, JE
    Dempsey, LA
    Platt, JL
    Prinz, RA
    Xu, XL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (11) : 8989 - 8998
  • [32] INTERPLAY OF SP1 AND EGR-1 IN THE PROXIMAL PLATELET-DERIVED GROWTH-FACTOR-A-CHAIN PROMOTER IN CULTURED VASCULAR ENDOTHELIAL-CELLS
    KHACHIGIAN, LM
    WILLIAMS, AJ
    COLLINS, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (46) : 27679 - 27686
  • [33] Early growth response factor 1: a pleiotropic mediator of inducible gene expression
    Khachigian, LM
    Collins, T
    [J]. JOURNAL OF MOLECULAR MEDICINE-JMM, 1998, 76 (09): : 613 - 616
  • [34] Egr-1 is activated in endothelial cells exposed to fluid shear stress and interacts with a novel shear-stress-response element in the PDGF A-chain promoter
    Khachigian, LM
    Anderson, KR
    Halnon, NJ
    Gimbrone, MA
    Resnick, N
    Collins, T
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (10) : 2280 - 2286
  • [35] PROTEOGLYCANS - STRUCTURES AND INTERACTIONS
    KJELLEN, L
    LINDAHL, U
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 : 443 - 475
  • [36] Kobayashi D, 2002, ANTICANCER RES, V22, P3963
  • [37] Koliopanos A, 2001, CANCER RES, V61, P4655
  • [38] A dominant negative Egr inhibitor blocks nerve growth factor-induced neurite outgrowth by suppressing c-Jun activation: Role of an Egr/c-Jun complex
    Levkovitz, Y
    Baraban, JM
    [J]. JOURNAL OF NEUROSCIENCE, 2002, 22 (10) : 3845 - 3854
  • [39] Heterodimer formation is essential for heparanase enzymatic activity
    Levy-Adam, F
    Miao, HQ
    Heinrikson, RL
    Vlodavsky, I
    Ilan, N
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 308 (04) : 885 - 891
  • [40] Transitions in histone acetylation reveal boundaries of three separately regulated neighboring loci
    Litt, MD
    Simpson, M
    Recillas-Targa, F
    Prioleau, MN
    Felsenfeld, G
    [J]. EMBO JOURNAL, 2001, 20 (09) : 2224 - 2235