Endoglin (CD105): a powerful therapeutic target on tumor-associated angiogenetic blood vessels

被引:214
作者
Fonsatti, E
Altomonte, M
Nicotra, MR
Natali, PG
Maio, M
机构
[1] IRCCS, Ctr Riferimento Oncol, Dept Med Oncol, Canc Bioimmunotherapy Unit, I-33081 Aviano, Italy
[2] CNR, Ist Biol & Patol Mol, I-00156 Rome, Italy
[3] Ist Regina Elena, Ctr Ric Sperimentale, Immunol Lab, I-00158 Rome, Italy
关键词
angiogenesis; CD105; endoglin; endothelial cells; soluble CD105; transforming growth factor;
D O I
10.1038/sj.onc.1206813
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
Among surface molecules expressed on endothelial cells, endoglin (CD105) is emerging as a prime vascular target for antiangiogenetic cancer therapy. CD105 is a cell membrane glycoprotein mainly expressed on endothelial cells and overexpressed on tumor-associated vascular endothelium, which functions as an accessory component of the transforming growth factor -beta receptor complex and is involved in vascular development and remodelling. Quanti. cation of intratumoral microvessel density by CD105 staining and of circulating soluble CD105 has been suggested to have prognostic significance in selected neoplasias. In addition, the potential usefulness of CD105 in tumor imaging and antiangiogenetic therapy has been well documented utilizing different animal models.
引用
收藏
页码:6557 / 6563
页数:7
相关论文
共 93 条
[1]   Analysis of ALK-1 and endoglin in newborns from families with hereditary hemorrhagic telangiectasia type 2 [J].
Abdalla, SA ;
Pece-Barbara, N ;
Vera, S ;
Tapia, E ;
Paez, E ;
Bernabeu, C ;
Letarte, M .
HUMAN MOLECULAR GENETICS, 2000, 9 (08) :1227-1237
[2]   Expression of endoglin mRNA and protein in human vascular smooth muscle cells [J].
Adam, PJ ;
Clesham, GJ ;
Weissberg, PL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 247 (01) :33-37
[3]   Estimation of angiogenesis with anti-CD105 immunostaining in the process of colorectal cancer development [J].
Akagi, K ;
Ikeda, Y ;
Sumiyoshi, Y ;
Kimura, Y ;
Kinoshita, J ;
Miyazaki, M ;
Abe, T .
SURGERY, 2002, 131 (01) :S109-S113
[4]   Expression and structural features of endoglin (CD105), a transforming growth factor beta 1 and beta 3 binding protein, in human melanoma [J].
Altomonte, M ;
Montagner, R ;
Fonsatti, E ;
Colizzi, F ;
Cattarossi, I ;
Brasoveanu, LI ;
Nicotra, MR ;
Cattelan, A ;
Natali, PG ;
Maio, M .
BRITISH JOURNAL OF CANCER, 1996, 74 (10) :1586-1591
[5]   Lack of specificity of endoglin expression for tumor blood vessels [J].
Balza, E ;
Castellani, P ;
Zulstra, A ;
Neri, D ;
Zardi, L ;
Siri, A .
INTERNATIONAL JOURNAL OF CANCER, 2001, 94 (04) :579-585
[6]   Endoglin is an accessory protein that interacts with the signaling receptor complex of multiple members of the transforming growth factor-β superfamily [J].
Barbara, NP ;
Wrana, JL ;
Letarte, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (02) :584-594
[7]   IDENTIFICATION AND EXPRESSION OF 2 FORMS OF THE HUMAN TRANSFORMING GROWTH FACTOR-BETA-BINDING PROTEIN ENDOGLIN WITH DISTINCT CYTOPLASMIC REGIONS [J].
BELLON, T ;
CORBI, A ;
LASTRES, P ;
CALES, C ;
CEBRIAN, M ;
VERA, S ;
CHEIFETZ, S ;
MASSAGUE, J ;
LETARTE, M ;
BERNABEU, C .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (09) :2340-2345
[8]   Mechanisms of disease:: Role of transforming growth factor β in human disease. [J].
Blobe, GC ;
Schiemann, WP ;
Lodish, HF .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (18) :1350-1358
[9]   Transcriptional activation of endoglin and transforming growth factor-β signaling components by cooperative interaction between Sp1 and KLF6:: their potential role in the response to vascular injury [J].
Botella, LM ;
Sánchez-Elsner, T ;
Sanz-Rodriguez, F ;
Kojima, S ;
Shimada, J ;
Guerrero-Esteo, M ;
Cooreman, MP ;
Ratziu, V ;
Langa, C ;
Vary, CPH ;
Ramírez, JR ;
Friedman, S ;
Bernabéu, C .
BLOOD, 2002, 100 (12) :4001-4010
[10]   Potential role of modifier genes influencing transforming growth factor-β1 levels in the development of vascular defects in endoglin heterozygous mice with hereditary hemorrhagic telangiectasia [J].
Bourdeau, A ;
Faughnan, ME ;
McDonald, ML ;
Paterson, AD ;
Wanless, IR ;
Letarte, M .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (06) :2011-2020