Endocan or endothelial cell specific molecule-1 (ESM-1): A potential novel endothelial cell marker and a new target for cancer therapy

被引:306
作者
Sarrazin, S
Adam, E
Lyon, M
Depontieu, F
Motte, V
Landolfi, C
Lortat-Jacob, H
Bechard, D
Lassalle, P
Delehedde, M
机构
[1] ENDOTIS PHARMA, Loos, France
[2] Inst Pasteur, INSERM, U416, F-59019 Lille, France
[3] Univ Manchester, Canc Res UK Dept Med Oncol, Manchester M20 4BX, Lancs, England
[4] Christie Hosp NHS Trust, Manchester M20 4BX, Lancs, England
[5] Inst Biol Sturct, F-38027 Grenoble, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2006年 / 1765卷 / 01期
关键词
endocan; ESM-1; proteoglycan; dermatan; cancer; inflammation; immunotherapy;
D O I
10.1016/j.bbcan.2005.08.004
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
Endocan, previously called endothelial cell specific molecule-1, is a soluble proteoglycan of 50 kDa, constituted of a mature polypeptide of 165 amino acids and a single dermatan sulphate chain covalently linked to the serine residue at position 137. This dermatan sulphate proteoglycan, which is expressed by the vascular endothelium, has been found freely circulating in the bloodstream of healthy subjects. Experimental evidence is accumulating that implicates endocan as a key player in the regulation of major processes such as cell adhesion, in inflammatory disorders and tumor progression. Inflammatory cytokines such as TNF-alpha, and pro-angiogenic growth factors such as VEGF, FGF-2 and HGF/SF, strongly increased the expression, synthesis or the secretion of endocan by human endothelial cells. Endocan is clearly overexpressed in human tumors, with elevated serum levels being observed in late-stage lung cancer patients, as measured by enzyme-linked immunoassay, and with its overexpression in experimental tumors being evident by immunohistochemistry. Recently, the mRNA levels of endocan have also been recognized as being one of the most significant molecular signatures of a bad prognosis in several types of cancer including lung cancer. Overexpression of this dermatan sulphate proteoglycan has also been shown to be directly involved in tumor progression as observed in mouse models of human tumor xenografts. Collectively, these results suggest that endocan could be a biomarker for both inflammatory disorders and tumor progression as well as a validated therapeutic target in cancer. On the basis of the recent successes of immunotherapeutic approaches in cancer, the preclinical data on endocan suggests that an antibody raised against the protein core of endocan could be a promising cancer therapy. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:25 / 37
页数:13
相关论文
共 93 条
[1]  
Adamia Sophia, 2005, Current Drug Targets - Cardiovascular & Haematological Disorders, V5, P3, DOI 10.2174/1568006053005056
[2]   Identification of endothelial cell genes expressed in an in vitro model of angiogenesis:: Induction of ESM-1, βig-h3, and NrCAM [J].
Aitkenhead, M ;
Wang, SJ ;
Nakatsu, MN ;
Mestas, J ;
Heard, C ;
Hughes, CCW .
MICROVASCULAR RESEARCH, 2002, 63 (02) :159-171
[3]   Tissue-wide expression profiling using cDNA subtraction and microarrays to identify tumor-specific genes [J].
Amatschek, S ;
Koenig, U ;
Auer, H ;
Steinlein, P ;
Pacher, M ;
Gruenfelder, A ;
Dekan, G ;
Vogl, S ;
Kubista, E ;
Heider, KH ;
Stratowa, C ;
Schreiber, M ;
Sommergruber, W .
CANCER RESEARCH, 2004, 64 (03) :844-856
[4]   Characterization of the secreted form of endothelial-cell-specific molecule 1 by specific monoclonal antibodies [J].
Bechard, D ;
Meignin, V ;
Scherpereel, A ;
Oudin, S ;
Kervoaze, G ;
Bertheau, P ;
Janin, A ;
Tonnel, AB ;
Lassalle, P .
JOURNAL OF VASCULAR RESEARCH, 2000, 37 (05) :417-425
[5]   Endocan is a novel chondroitin sulfate/dermatan sulfate proteoglycan that promotes hepatocyte growth factor/scatter factor mitogenic activity [J].
Béchard, D ;
Gentina, T ;
Delehedde, M ;
Scherpereel, A ;
Lyon, M ;
Aumercier, M ;
Vazeux, R ;
Richet, C ;
Degand, P ;
Jude, B ;
Janin, A ;
Fernig, DG ;
Tonnel, AB ;
Lassalle, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (51) :48341-48349
[6]   Human endothelial-cell specific molecule-1 binds directly to the integrin CD11a/CD18 (LFA-1) and blocks binding to intercellular adhesion molecule-1 [J].
Béchard, D ;
Scherpereel, A ;
Hammad, H ;
Gentina, T ;
Tsicopoulos, A ;
Aumercier, M ;
Pestel, J ;
Dessaint, JP ;
Tonnel, AB ;
Lassalle, P .
JOURNAL OF IMMUNOLOGY, 2001, 167 (06) :3099-3106
[7]   Stromal fibroblasts in cancer initiation and progression [J].
Bhowmick, NA ;
Neilson, EG ;
Moses, HL .
NATURE, 2004, 432 (7015) :332-337
[8]   Molecular signatures in biopsy specimens of lung cancer [J].
Borczuk, AC ;
Shah, L ;
Pearson, GDN ;
Walter, KL ;
Wang, LQ ;
Austin, JHM ;
Friedman, RA ;
Powell, CA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (02) :167-174
[9]   Splice variants as cancer biomarkers [J].
Brinkman, BMN .
CLINICAL BIOCHEMISTRY, 2004, 37 (07) :584-594
[10]   Presentation of IFN-γ to nitric oxide-producing cells:: A novel function for mast cells [J].
Brooks, B ;
Briggs, DM ;
Eastmond, NC ;
Fernig, DG ;
Coleman, JW .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :573-579