Angiogenesis of gastrointestinal tumours and their metastases - a target for intervention?

被引:24
作者
Garcea, G
Lloyd, TD
Gescher, A
Dennison, AR
Steward, WP
Berry, DP
机构
[1] Leicester Royal Infirm, Leicester LE2 7LX, Leics, England
[2] Leicester Gen Hosp, Dept Hepatobiliary Surg, Leicester LE5 4PW, Leics, England
关键词
colorectal cancer; pancreatic cancer; gastrointestinal cancer; angiogenesis and anti-angiogenesis therapy;
D O I
10.1016/j.ejca.2004.02.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis is an obligatory event for the growth of tumours beyond 2 mm in diameter, above which simple oxygen diffusion can no longer support the rapid proliferation of malignant cells. Angiogenesis is a fine balance between inhibitory and stimulatory factors, the knowledge of which offers novel targets for the treatment of gastrointestinal neoplasia. A literature search of Pubmed and Medline databases was undertaken, using the keywords colorectal cancer, pancreatic cancer, gastrointestinal cancer, angiogenesis and anti-angiogenesis therapy. It was found that angiogenesis in primary tumours is a sequential and highly complex cascade of molecular events resulting in the rapid exponential growth of the tumour. Hepatic metastases of primary tumours may be less reliant on traditional angiogenic pathways, by co-opting pre-existing hepatic vasculature. Research into angiogenesis has revealed many different sites that can be targeted by agents such as tyrosine kinase inhibitors. Many anti-angiogenic agents are undergoing preclinical evaluation, with only a few entering phase I and phase III clinical trials. However, early results suggest that anti-angiogenic therapy could be an important adjunct to conventional chemotherapy treatment of gastrointestinal neoplasia. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1302 / 1313
页数:12
相关论文
共 158 条
[31]   Vessel counts and vascular endothelial growth factor expression in pancreatic adenocarcinoma [J].
Ellis, LM ;
Takahashi, Y ;
Fenoglio, CJ ;
Cleary, KR ;
Bucana, CD ;
Evans, DB .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (03) :337-340
[32]  
Ellis LM, 2002, ONCOLOGY-NY, V16, P31
[33]  
Estival A, 1997, CANCER DETECT PREV, V21, P546
[34]  
Etoh T, 2001, CANCER RES, V61, P2145
[35]   Expression of vascular endothelial growth factor receptors in human prostate cancer [J].
Ferrer, FA ;
Miller, LJ ;
Lindquist, R ;
Kowalczyk, P ;
Laudone, VP ;
Albertsen, PC ;
Kreutzer, DL .
UROLOGY, 1999, 54 (03) :567-572
[36]  
FOLKMAN J, 1986, CANCER RES, V46, P467
[37]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[38]   WHAT IS THE EVIDENCE THAT TUMORS ARE ANGIOGENESIS DEPENDENT [J].
FOLKMAN, J .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (01) :4-6
[39]   Expression of two angiogenic factors, vascular endothelial growth factor and platelet-derived endothelial cell growth factor in human pancreatic cancer, and its relationship to angiogenesis [J].
Fujimoto, K ;
Hosotani, R ;
Wada, M ;
Lee, JU ;
Koshiba, T ;
Miyamoto, Y ;
Tsuji, S ;
Nakajima, S ;
Doi, R ;
Imamura, M .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (09) :1439-1447
[40]  
Fujioka S, 2001, CANCER, V92, P1788, DOI 10.1002/1097-0142(20011001)92:7<1788::AID-CNCR1695>3.0.CO