Platelet-derived growth factor receptor (PDGFR): A target for anticancer therapeutics

被引:119
作者
Board, R [1 ]
Jayson, GC [1 ]
机构
[1] Christie Hosp, Canc Res UK Dept Med Oncol, Manchester M20 4BX, Lancs, England
关键词
PDGF; PDGFR; interstitial fluid pressure; cancer; angiogenesis;
D O I
10.1016/j.drup.2005.03.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Platelet-derived growth factors (PDGFs) and their tyrosine kinase receptors (PDGFRs) have been implicated in the pathogenesis of a number of tumor types and play an important role in angiogenesis. Tumor growth can be promoted by PDGF via autocrine stimulation of malignant cells, by overexpression or overactivation of PDGFRs, or by stimulation of angiogenesis within the tumor. These mechanisms could provide possible therapeutic targets. PDGFR blockade may also lower the interstitial fluid pressure within solid tumors and enhance drug delivery. Here we discuss the possible therapeutic roles of PDGFR antagonists in the treatment of cancer, alone and in combination with chemotherapy or other targeted agents. Extensive experimental data highlight the potential therapeutic advantage of targeting PDGFR. However, recent clinical data suggest that antagonism of this growth factor is associated with fluid accumulation that could obscure any clinical benefit. Further clinical research is required to optimise inhibition of this cytokine-receptor system. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:75 / 83
页数:9
相关论文
共 79 条
[1]  
Abrams TJ, 2003, MOL CANCER THER, V2, P1011
[2]   Endothelial and nonendothelial sources of PDGF-B regulate pericyte recruitment and influence vascular pattern formation in tumors [J].
Abramsson, A ;
Lindblom, P ;
Betsholtz, C .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (08) :1142-1151
[3]   Vascular remodeling and clinical resistance to antiangiogenic cancer therapy [J].
Bender, JG ;
Cooney, EM ;
Kandel, JJ ;
Yamashiro, DJ .
DRUG RESISTANCE UPDATES, 2004, 7 (4-5) :289-300
[4]   Tumorigenesis and the angiogenic switch [J].
Bergers, G ;
Benjamin, LE .
NATURE REVIEWS CANCER, 2003, 3 (06) :401-410
[5]   PDGF-D is a specific, protease-activated ligand for the PDGF β-receptor [J].
Bergsten, E ;
Uutela, M ;
Li, XR ;
Pietras, K ;
Östman, A ;
Heldin, CH ;
Alitalo, K ;
Eriksson, U .
NATURE CELL BIOLOGY, 2001, 3 (05) :512-516
[6]   Insight into the physiological functions of PDGF through genetic studies in mice [J].
Betsholtz, C .
CYTOKINE & GROWTH FACTOR REVIEWS, 2004, 15 (04) :215-228
[7]   CDNA SEQUENCE AND CHROMOSOMAL LOCALIZATION OF HUMAN PLATELET-DERIVED GROWTH-FACTOR A-CHAIN AND ITS EXPRESSION IN TUMOR-CELL LINES [J].
BETSHOLTZ, C ;
JOHNSSON, A ;
HELDIN, CH ;
WESTERMARK, B ;
LIND, P ;
URDEA, MS ;
EDDY, R ;
SHOWS, TB ;
PHILPOTT, K ;
MELLOR, AL ;
KNOTT, TJ ;
SCOTT, J .
NATURE, 1986, 320 (6064) :695-699
[8]   Regulation of PDGF and its receptors in fibrotic diseases [J].
Bonner, JC .
CYTOKINE & GROWTH FACTOR REVIEWS, 2004, 15 (04) :255-273
[9]  
BRAHMER JR, 2002, P AN M AM SOC CLIN, V21, P335
[10]  
BRITTEN CD, 2002, P AN M AM SOC CLIN, V21, P1922