Tumor angiogenesis and anti-angiogenic therapy

被引:6
作者
Guo, Ziheng [1 ]
Jing, Xu [2 ]
Sun, Xiaoting [2 ,3 ]
Sun, Shishuo [2 ,4 ]
Yang, Yunlong [5 ]
Cao, Yihai [2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Pancreat Surg, Chengdu 610041, Sichuan, Peoples R China
[2] Karolinska Inst, Dept Microbiol Tumor & Cell Biol, S-17177 Stockholm, Sweden
[3] Wenzhou Med Univ, Sch Pharmaceut Sci, Oujiang Lab, Zhejiang Lab Regenerat Med Vis & Brain Hlth, Wenzhou 325035, Zhejiang, Peoples R China
[4] Xuzhou Med Univ, Canc Inst, Clin Med Coll 1, Xuzhou 221000, Jiangsu, Peoples R China
[5] Fudan Univ, Sch Basic Med Sci, Dept Cellular & Genet Med, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金; 瑞典研究理事会; 欧洲研究理事会;
关键词
Angiogenesis; Cancer; Angiogenesis inhibitors; Angiogenic factors; Vascular endothelial growth factors; Cancer therapy; Combined modality therapy; ENDOTHELIAL GROWTH-FACTOR; RANDOMIZED PHASE-III; VASCULAR-PERMEABILITY FACTOR; PROTEASE-ACTIVATED LIGAND; PLUS BEVACIZUMAB; TIE2; RECEPTOR; BEARING MICE; IN-VIVO; VEGF; INHIBITOR;
D O I
10.1097/CM9.0000000000003231
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Anti-angiogenic drugs (AADs), which mainly target the vascular endothelial growth factor-A signaling pathway, have become a therapeutic option for cancer patients for two decades. During this period, tremendous clinical experience of anti-angiogenic therapy has been acquired, new AADs have been developed, and the clinical indications for AAD treatment of various cancers have been expanded using monotherapy and combination therapy. However, improvements in the therapeutic outcomes of clinically available AADs and the development of more effective next-generation AADs are still urgently required. This review aims to provide historical and perspective views on tumor angiogenesis to allow readers to gain mechanistic insights and learn new therapeutic development. We revisit the history of concept initiation and AAD discovery, and summarize the up-to-date clinical translation of anti-angiogenic cancer therapy in this field.
引用
收藏
页码:2043 / 2051
页数:9
相关论文
共 135 条
[1]  
ALGIRE GH, 1950, JNCI-J NATL CANCER I, V11, P555
[2]   Endostar (rh-endostatin) versus placebo in combination with vinorelbine plus cisplatin chemotherapy regimen in treatment of advanced non-small cell lung cancer: A meta-analysis [J].
An, Jihong ;
Lv, Weiling .
THORACIC CANCER, 2018, 9 (05) :606-612
[3]   The clinical trial landscape for PD1/PDL1 immune checkpoint inhibitors [J].
Tang, Jun ;
Yu, Jia Xin ;
Lin, Yunqing .
NATURE REVIEWS DRUG DISCOVERY, 2018, 17 (12) :854-854
[4]   TUMOR-INDUCED ANGIOGENESIS - LACK OF INHIBITION BY IRRADIATION [J].
AUERBACH, R ;
ARENSMAN, R ;
KUBAI, L ;
FOLKMAN, J .
INTERNATIONAL JOURNAL OF CANCER, 1975, 15 (02) :241-245
[5]   The FGF family: biology, pathophysiology and therapy [J].
Beenken, Andrew ;
Mohammadi, Moosa .
NATURE REVIEWS DRUG DISCOVERY, 2009, 8 (03) :235-253
[6]   Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[7]   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
[8]   ISOLATION AND PARTIAL MOLECULAR CHARACTERIZATION OF PITUITARY FIBROBLAST GROWTH-FACTOR [J].
BOHLEN, P ;
BAIRD, A ;
ESCH, F ;
LING, N ;
GOSPODAROWICZ, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (17) :5364-5368
[9]   Angiogenesis inhibitor, TNP-470, prevents diet-induced and genetic obesity in mice [J].
Bråkenhielm, E ;
Cao, RH ;
Gao, BH ;
Angelin, B ;
Cannon, B ;
Parini, P ;
Cao, YH .
CIRCULATION RESEARCH, 2004, 94 (12) :1579-1588
[10]   INHIBITION OF TUMOR ANGIOGENESIS MEDIATED BY CARTILAGE [J].
BREM, H ;
FOLKMAN, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1975, 141 (02) :427-439