Mechanisms of disease: angiogenesis in urologic malignancies

被引:44
作者
Charlesworth, PJS [1 ]
Harris, AL
机构
[1] John Radcliffe & Churchill Hosp, Wetherall Inst Mol Med, Oxford OX3 9DS, England
[2] John Radcliffe & Churchill Hosp, Oncol Dept, Oxford OX3 9DS, England
来源
NATURE CLINICAL PRACTICE UROLOGY | 2006年 / 3卷 / 03期
关键词
angiogenesis; bladder cancer; prostate cancer; renal cancer;
D O I
10.1038/ncpuro0434
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Angiogenesis is critical for growth of tumors and their metastasis. In this article we review the literature on studies of angiogenesis pathways and markers for renal cancer, prostate cancer and bladder cancer. Overall, there is clear evidence that markers of angiogenesis and expression of angiogenic factors are associated with adverse outcomes in each of these tumor types. Relatively few angiogenic pathways have been investigated so far, although over 50 factors are known to be involved, and little has been studied on the antiangiogenic pathways and their suppression. The failing in many of the studies is small size and lack of suitable statistical analysis. Nevertheless, this review demonstrates the importance of these pathways and the need to develop selection criteria for patients who are candidates for antiangiogenic therapies. On the basis of the expression profiles reported so far, therapies that target vascular endothelial growth factor should be considered for the treatment of renal, prostate and bladder cancers. As most tumors express factors that are involved in multiple angiogenic pathways, further research is needed to determine which are coregulated and what the most common patterns are.
引用
收藏
页码:157 / 169
页数:13
相关论文
共 104 条
[1]   Tissue factor expression and angiogenesis in human prostate carcinoma [J].
Abdulkadir, SA ;
Carvalhal, GF ;
Kaleem, Z ;
Kisiel, W ;
Humphrey, PA ;
Catalona, WJ ;
Milbrandt, J .
HUMAN PATHOLOGY, 2000, 31 (04) :443-447
[2]  
Arima J, 2000, CANCER, V88, P1131
[3]   Carbonic anhydrase IX expression predicts outcome of interleukin 2 therapy for renal cancer [J].
Atkins, M ;
Regan, M ;
McDermott, D ;
Mier, J ;
Stanbridge, E ;
Youmans, A ;
Febbo, P ;
Upton, M ;
Lechpammer, M ;
Signoretti, S .
CLINICAL CANCER RESEARCH, 2005, 11 (10) :3714-3721
[4]  
Bakkar AA, 2003, CANCER RES, V63, P8108
[5]   Tumorigenesis and the angiogenic switch [J].
Bergers, G ;
Benjamin, LE .
NATURE REVIEWS CANCER, 2003, 3 (06) :401-410
[6]   Serum levels of vascular endothelial growth factor as a prognostic factor in bladder cancer [J].
Bernardini, S ;
Fauconnet, S ;
Chabannes, E ;
Henry, PC ;
Adessi, G ;
Bittard, H .
JOURNAL OF UROLOGY, 2001, 166 (04) :1275-1279
[7]   Novel angiogenic signaling pathways and vascular targets [J].
Bicknell, R ;
Harris, AL .
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 2004, 44 :219-238
[8]   ANGIOGENESIS IN BLADDER-CANCER - RELATIONSHIP BETWEEN MICROVESSEL DENSITY AND TUMOR PROGNOSIS [J].
BOCHNER, BH ;
COTE, RJ ;
WEIDNER, N ;
GROSHEN, S ;
CHEN, SC ;
SKINNER, DG ;
NICHOLS, PW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (21) :1603-1612
[9]   Changes in circulating dendritic cells and IL-12 in relation to the angiogenic factor VEGF during IL-2 immunotherapy of metastatic renal cell cancer [J].
Bonfanti, A ;
Lissoni, P ;
Bucovec, R ;
Rovelli, F ;
Brivio, F ;
Fumagalli, L .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2000, 15 (02) :161-164
[10]   Microvessel density in prostate carcinoma [J].
Bono, AV ;
Celato, N ;
Cova, V ;
Salvadore, M ;
Chinetti, S ;
Novario, R .
PROSTATE CANCER AND PROSTATIC DISEASES, 2002, 5 (02) :123-127