Angiopoietins in malignancy

被引:70
作者
Bach, F. [1 ]
Uddin, F. J. [1 ]
Burke, D. [1 ]
机构
[1] Leeds Gen Infirm, Acad Dept Surg, Leeds LS1 3EX, W Yorkshire, England
来源
EJSO | 2007年 / 33卷 / 01期
关键词
angiopoietins; cancer; tumour vascularity;
D O I
10.1016/j.ejso.2006.07.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Tumour growth is dependant upon the development of an adequate blood supply. This, in turn, is thought to depend upon a switch by the tumour, from a dormant to angiogenic state. Recent data suggest that this switch may occur when the balance of pro- and anti-angiogenic agents alters to promote angiogenesis. Angiopoietins may be involved in this balance. Methods: An electronic literature search was performed with respect to angiopoietins from 1996 to the present. Published data from in-vitro and in-vivo studies were critically analysed. A specific focus was made of studies relating to tumour growth and vasculature. Results: Since angiopoietin-1 was first described in 1996, three more angiopoietins have been described. All family members bind to the Tie-2 receptor. There is now a considerable accumulation of data that suggests they play a pivotal role in the development and stabilisation of tumour vasculature. angiopoietin-2 appears to be pro-angiogenic whilst angiopoietin-1 appears to be a stabilising factor. Conclusions: Recent trials of anti-angiogenic agents show promise in the treatment of solid human cancers. The angiopoietins are a new family of proteins that appear to be influential in the development of the tumour vasculature. Manipulation of the angiopoietin balance may provide a potential therapeutic target in human cancer. (C) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7 / 15
页数:9
相关论文
共 64 条
[1]  
Ahmad SA, 2001, CANCER, V92, P1138, DOI 10.1002/1097-0142(20010901)92:5<1138::AID-CNCR1431>3.0.CO
[2]  
2-L
[3]  
Ahmad SA, 2001, CANCER RES, V61, P1255
[4]   The tie receptor tyrosine kinase is expressed by human hematopoietic progenitor cells and by a subset of megakaryocytic cells [J].
Batard, P ;
Sansilvestri, P ;
Scheinecker, C ;
Knapp, W ;
Debili, N ;
Vainchenker, W ;
Buhring, HJ ;
Monier, MN ;
Kukk, E ;
Partanen, J ;
Matikainen, MT ;
Alitalo, R ;
Hatzfeld, J ;
Alitalo, K .
BLOOD, 1996, 87 (06) :2212-2220
[5]  
Borre M, 2000, CLIN CANCER RES, V6, P1882
[6]   Expression of Tie1, Tie2, and angiopoietins 1, 2, and 4 in Kaposi's sarcoma and cutaneous angiosarcoma [J].
Brown, LF ;
Dezube, BJ ;
Tognazzi, K ;
Dvorak, HF ;
Yancopoulos, GD .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (06) :2179-2183
[7]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[8]   Expression of the angiopoietins and their receptor Tie2 in human renal clear cell carcinomas; regulation by the von Hippel-Lindau gene and hypoxia [J].
Currie, MJ ;
Gunningham, SP ;
Turner, K ;
Han, C ;
Scott, PAE ;
Robinson, BA ;
Chong, W ;
Harris, AL ;
Fox, SB .
JOURNAL OF PATHOLOGY, 2002, 198 (04) :502-510
[9]   Isolation of Angiopoietin-1, a ligand for the TIE2 receptor, by secretion-trap expression cloning [J].
Davis, S ;
Aldrich, TH ;
Jones, PF ;
Acheson, A ;
Compton, DL ;
Jain, V ;
Ryan, TE ;
Bruno, J ;
Radziejewski, C ;
Maisonpierre, PC ;
Yancopoulos, GD .
CELL, 1996, 87 (07) :1161-1169
[10]  
Davis S, 1999, CURR TOP MICROBIOL, V237, P173