Evading tumor evasion: Current concepts and perspectives of anti-angiogenic cancer therapy

被引:198
作者
Abdollahi, Amir [1 ,2 ,3 ,4 ,5 ]
Folkman, Judah [2 ,3 ]
机构
[1] Tufts Univ, St Elizabeths Med Ctr, Sch Med, Dept Med,Ctr Canc Syst Biol, Boston, MA 02135 USA
[2] Childrens Hosp, Dept Surg, Vasc Biol Program, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Boston, MA 02115 USA
[4] Heidelberg Univ, Dept Radiat Oncol, Sch Med, Heidelberg Ion Therapy Ctr HIT, D-69120 Heidelberg, Germany
[5] German Canc Res Ctr, NCT, D-69120 Heidelberg, Germany
关键词
Angiogenesis; Resistance; Stroma; Radiotherapy; Metastasis; Invasion; Evolution; Sunitinib; Bevacizumab; TYROSINE KINASE INHIBITOR; GROWTH-FACTOR RECEPTOR; ENDOTHELIAL-CELLS; BREAST-CANCER; SUNITINIB MALATE; PATHOLOGICAL ANGIOGENESIS; GLUCOSYLCERAMIDE SYNTHASE; ANTIANGIOGENIC THERAPY; VASCULAR ENDOTHELIUM; HORIZONTAL TRANSFER;
D O I
10.1016/j.drup.2009.12.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Within three decades, anti-angiogenic therapy has rapidly evolved into an integral component of current standard anti-cancer treatment Ann-angiogenic therapy has fulfilled a number of its earlier proposed promises The universality of this approach is demonstrated by the broad spectrum of malignant and benign tumor entitles, as well as non-neoplastic diseases, that are currently treated with anti-angiogenic agents In contrast to tumor cell targeting therapies, the development of acquired drug resistance (e g via mutations in growth factor receptor signaling genes) has not been described yet for the principal target of anti-angiogenic therapy the tumor endothelium. Moreover, the tumor endothelium has emerged as a critical target of conventional cancer therapies, such as chemotherapy and radiotherapy The presumption that tumor growth and metastasis are angiogenesis-dependent implies that the number of potential targets of an anti-cancer therapy could be reduced to those that stimulate the angiogenesis process Therefore, the set of endogenous angiogenesis stimulants might constitute an "Achilles heel" of cancer. Direct targeting of tumor endothelium via, e.g., endogenous angiogenesis Inhibitors poses another promising but clinically less explored therapeutic strategy. Indeed, the majority of current anti-angiogenic approaches block the activity of a single or at most a few pro-angiogenic proteins secreted by tumor cells or the tumor stroma. Based on our systems biology work on the angiogenic switch, we predicted that the redundancy of angiogenic signals might limit the efficacy of anti-angiogenic monotherapies In support of this hypothesis, emerging experimental evidence suggests that tumors may become refractory or even evade the inhibition of a single pro-angiogenic pathway via compensatory upregulation of alternative angiogenic factors. Here, we discuss current concepts and propose novel strategies to overcome tumor evasion of anti-angiogenic therapy. We believe that early detection of tumors, prediction of tumor evasive mechanisms and rational design of anti-angiogenic combinations will direct anti-angiogenic therapy towards its ultimate goal the conversion of cancer to a dormant, chronic, manageable disease. (C) 2009 Elsevier Ltd All rights reserved
引用
收藏
页码:16 / 28
页数:13
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