Modes of resistance to anti-angiogenic therapy

被引:2358
作者
Bergers, Gabriele [1 ,4 ]
Hanahan, Douglas [2 ,3 ,4 ]
机构
[1] Univ Calif San Francisco, Dept Neurol Surg, Brain Tumor Res Ctr, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Ctr Diabet, San Francisco, CA 94143 USA
[4] UCSF Helen Diller Comprehens Canc Ctr, San Francisco, CA 94143 USA
关键词
D O I
10.1038/nrc2442
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis inhibitors targeting the vascular endothelial growth factor (VEGF) signalling pathways are affording demonstrable therapeutic efficacy in mouse models of cancer and in an increasing number of human cancers. However, in both preclinical and clinical settings, the benefits are at best transitory and are followed by a restoration of tumour growth and progression. Emerging data support a proposition that two modes of unconventional resistance underlie such results: evasive resistance, an adaptation to circumvent the specific angiogenic blockade; and intrinsic or pre-existing indifference. Multiple mechanisms can be invoked in different tumour contexts to manifest both evasive and intrinsic resistance, motivating assessment of their prevalence and importance and in turn the design of pharmacological strategies that confer enduring anti-angiogenic therapies.
引用
收藏
页码:592 / 603
页数:12
相关论文
共 102 条
[1]   Tumor stromal-derived factor-1 recruits vascular progenitors to mitotic neovasculature, where microenvironment influences their differentiated phenotypes [J].
Aghi, Manish ;
Cohen, Kenneth S. ;
Klein, Rachael J. ;
Scadden, David T. ;
Chioccra, E. Antonio .
CANCER RESEARCH, 2006, 66 (18) :9054-9064
[2]   Pericytes: Cell biology and pathology [J].
Allt, G ;
Lawrenson, JG .
CELLS TISSUES ORGANS, 2001, 169 (01) :1-11
[3]  
Apte RS, 2008, EXPERT OPIN PHARMACO, V9, P499, DOI [10.1517/14656566.9.3.499, 10.1517/14656566.9.3.499 ]
[4]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[5]   Integrins in angiogenesis and lymphangiogenesis [J].
Avraamides, Christie J. ;
Garmy-Susini, Barbara ;
Varner, Judith A. .
NATURE REVIEWS CANCER, 2008, 8 (08) :604-617
[6]   Cellular abnormalities of blood vessels as targets in cancer [J].
Baluk, P ;
Hashizume, H ;
McDonald, DM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2005, 15 (01) :102-111
[7]   AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients [J].
Batchelor, Tracy T. ;
Sorensen, A. Gregory ;
di Tomaso, Emmanuelle ;
Zhang, Wei-Ting ;
Duda, Dan G. ;
Cohen, Kenneth S. ;
Kozak, Kevin R. ;
Cahill, Daniel P. ;
Chen, Poe-Jou ;
Zhu, Mingwang ;
Ancukiewicz, Marek ;
Mrugala, Maciej M. ;
Plotkin, Scott ;
Drappatz, Jan ;
Louis, David N. ;
Ivy, Percy ;
Scadden, David T. ;
Benner, Thomas ;
Loeffler, Jay S. ;
Wen, Patrick Y. ;
Jain, Rakesh K. .
CANCER CELL, 2007, 11 (01) :83-95
[8]   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
[9]  
Benjamin LE, 1998, DEVELOPMENT, V125, P1591
[10]  
Berger MS, 1999, GLIOMAS