Regulation of VEGF/VPF expression in tumor cells: Consequences for tumor growth and metastasis

被引:167
作者
Claffey, KP
Robinson, GS
机构
[1] HARVARD UNIV, SCH MED, DEPT PATHOL, BOSTON, MA 02215 USA
[2] HYBRIDON INC, WORCESTER, MA 01605 USA
关键词
angiogenesis; cancer; hypoxia; melanoma; metastasis; VEGF; VPF;
D O I
10.1007/BF00437469
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Vascular endothelial growth factor (VEGF), also known as vascular permeability factor (VPF) is a multifunctional cytokine which potently stimulates angiogenesis in vivo. VEGF/VPF expression is elevated in pathological conditions including cancer, proliferative retinopathy, psoriasis and rheumatoid arthritis. The angiogenesis associated with human tumors is likely a central component in promoting tumor growth and metastatic potential. The regulation of VEGF/VPF expression during tumor progression may involve diverse mechanisms including activated oncogenes, mutant or deleted tumor suppressor genes, cytokine activation, hormonal modulators, and a particularly effective activator, hypoxia. Understanding the diverse mechanisms by which tumor cells overexpress VEGF/VPF and which mechanisms are operating in specific tumor types is important for the design of effective anti-cancer therapies.
引用
收藏
页码:165 / 176
页数:12
相关论文
共 108 条
[91]   CLONAL EXPANSION OF P53 MUTANT-CELLS IS ASSOCIATED WITH BRAIN-TUMOR PROGRESSION [J].
SIDRANSKY, D ;
MIKKELSEN, T ;
SCHWECHHEIMER, K ;
ROSENBLUM, ML ;
CAVANEE, W ;
VOGELSTEIN, B .
NATURE, 1992, 355 (6363) :846-848
[92]   HYPOXIA AND PLATELET-DERIVED GROWTH FACTOR-BB SYNERGISTICALLY UP-REGULATE THE EXPRESSION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR IN VASCULAR SMOOTH-MUSCLE CELLS [J].
STAVRI, GT ;
HONG, Y ;
ZACHARY, IC ;
BREIER, G ;
BASKERVILLE, PA ;
YLAHERTTUALA, S ;
RISAU, W ;
MARTIN, JF ;
ERUSALIMSKY, JD .
FEBS LETTERS, 1995, 358 (03) :311-315
[93]   BASIC FIBROBLAST GROWTH-FACTOR UP-REGULATES THE EXPRESSION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR IN VASCULAR SMOOTH-MUSCLE CELLS - SYNERGISTIC INTERACTION WITH HYPOXIA [J].
STAVRI, GT ;
ZACHARY, IC ;
BASKERVILLE, PA ;
MARTIN, JF ;
ERUSALIMSKY, JD .
CIRCULATION, 1995, 92 (01) :11-14
[94]  
STEIN I, 1995, MOL CELL BIOL, V15, P5363
[95]   DEVELOPMENT OF RETINAL VASCULATURE IS MEDIATED BY HYPOXIA-INDUCED VASCULAR ENDOTHELIAL GROWTH-FACTOR (VEGF) EXPRESSION BY NEUROGLIA [J].
STONE, J ;
ITIN, A ;
ALON, T ;
PEER, J ;
GNESSIN, H ;
CHANLING, T ;
KESHET, E .
JOURNAL OF NEUROSCIENCE, 1995, 15 (07) :4738-4747
[96]   ENHANCED EXPRESSION OF MULTIPLE FORMS OF VEGF IS ASSOCIATED WITH SPONTANEOUS IMMORTALIZATION OF MURINE FIBROBLASTS [J].
SUGIHARA, T ;
KAUL, SC ;
MITSUI, Y ;
WADHWA, R .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 1994, 1224 (03) :365-370
[97]   IDENTIFICATION OF THE KDR TYROSINE KINASE AS A RECEPTOR FOR VASCULAR ENDOTHELIAL-CELL GROWTH-FACTOR [J].
TERMAN, BI ;
DOUGHERVERMAZEN, M ;
CARRION, ME ;
DIMITROV, D ;
ARMELLINO, DC ;
GOSPODAROWICZ, D ;
BOHLEN, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1992, 187 (03) :1579-1586
[98]  
TISCHER E, 1991, J BIOL CHEM, V266, P11947
[99]  
Toi M, 1995, CLIN CANCER RES, V1, P961
[100]   TUMOR ANGIOGENESIS IN BREAST-CANCER - ITS IMPORTANCE AS A PROGNOSTIC INDICATOR AND THE ASSOCIATION WITH VASCULAR ENDOTHELIAL GROWTH-FACTOR EXPRESSION [J].
TOI, M ;
INADA, K ;
SUZUKI, H ;
TOMINAGA, T .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 36 (02) :193-204