Development of SU5416, a selective small molecule inhibitor of VEGF receptor tyrosine kinase activity, as an anti-angiogenesis agent

被引:0
作者
Mendel, DB
Laird, AD
Smolich, BD
Blake, RA
Liang, CX
Hannah, AL
Shaheen, RM
Ellis, LM
Weitman, S
Shawver, LK
Cherrington, JM
机构
[1] SUGEN Inc, Preclin Therapeut, S San Francisco, CA 94080 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Surg Oncol & Canc Biol, Houston, TX 77030 USA
[3] Canc Therapy & Res Ctr, Inst Drug Dev, San Antonio, TX 78245 USA
来源
ANTI-CANCER DRUG DESIGN | 2000年 / 15卷 / 01期
关键词
angiogenesis; cancer; indolinones; SU5416;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Angiogenesis, or the sprouting of new blood vessels, is a central process in the growth of solid tumors. For many cancers, the extent of vascularization of a tumor is a negative prognostic indicator signifying aggressive disease and increased potential for metastasis, Recent efforts to understand the molecular basis of tumor-associated angiogenesis have identified several potential therapeutic targets, including the receptor tyrosine kinases for the angiogenic factor vascular endothelial growth factor (VEGF). Here we review the approach taken at SUGEN. Inc. to discover and develop small molecule inhibitors of receptor tyrosine kinases as anti-angiogenic agents. We focus on SU5416, a selective inhibitor of VEGF receptors that is currently in clinical development for the treatment of advanced malignancies. Its biochemical, biological and pharmacological properties are reviewed and clinical implications discussed.
引用
收藏
页码:29 / 41
页数:13
相关论文
共 35 条
[31]   Calcitriol (1,25-dihydroxycholecalciferol) enhances mast cell tumour chemotherapy and receptor tyrosine kinase inhibitor activity in vitro and has single-agent activity against spontaneously occurring canine mast cell tumours [J].
Malone, E. K. ;
Rassnick, K. M. ;
Wakshlag, J. J. ;
Russell, D. S. ;
Al-Sarraf, R. ;
Ruslander, D. M. ;
Johnson, C. S. ;
Trump, D. L. .
VETERINARY AND COMPARATIVE ONCOLOGY, 2010, 8 (03) :209-220
[32]   Inhibition of insulin-like growth factor-I receptor (IGF-IR) using NVP-AEW541, a small molecule kinase inhibitor, reduces orthotopic pancreatic cancer growth and angiogenesis [J].
Moser, Christian ;
Schachtschneider, Philipp ;
Lang, Sven A. ;
Gaumann, Andreas ;
Mori, Akira ;
Zimmermann, Johann ;
Schlitt, Hans J. ;
Geissler, Edward K. ;
Stoeltzing, Oliver .
EUROPEAN JOURNAL OF CANCER, 2008, 44 (11) :1577-1586
[33]   BMS-690514, a VEGFR and EGFR tyrosine kinase inhibitor, shows anti-tumoural activity on non-small-cell lung cancer xenografts and induces sequence-dependent synergistic effect with radiation [J].
Loriot, Y. ;
Mordant, P. ;
Dorvault, N. ;
Rouge, T. De la Motte ;
Bourhis, J. ;
Soria, J-C ;
Deutsch, E. .
BRITISH JOURNAL OF CANCER, 2010, 103 (03) :347-353
[34]   Biologic and Clinical Activity of Tivozanib (AV-951, KRN-951), a Selective Inhibitor of VEGF Receptor-1,-2, and -3 Tyrosine Kinases, in a 4-Week-On, 2-Week-Off Schedule in Patients with Advanced Solid Tumors [J].
Eskens, Ferry A. L. M. ;
de Jonge, Maja J. A. ;
Bhargava, Pankaj ;
Isoe, Toshiyuki ;
Cotreau, Monette M. ;
Esteves, Brooke ;
Hayashi, Kunihiko ;
Burger, Herman ;
Thomeer, Maarten ;
van Doorn, Leni ;
Verweij, Jaap .
CLINICAL CANCER RESEARCH, 2011, 17 (22) :7156-7163
[35]   Synthesis and Biological Profile of the pan-Vascular Endothelial Growth Factor Receptor/Tyrosine Kinase with Immunoglobulin and Epidermal Growth Factor-Like Homology Domains 2 (VEGF-R/TIE-2) Inhibitor 11-(2-Methylpropyl)-12,13-dihydro-2-methyl-8-(pyrimidin-2-ylamino)-4H-indazolo[5,4-a]pyrrolo[3,4-c]carbazol-4-one (CEP-11981): A Novel Oncology Therapeutic Agent [J].
Hudkins, Robert L. ;
Becknell, Nadine C. ;
Zulli, Allison L. ;
Underiner, Ted L. ;
Angeles, Thelma S. ;
Aimone, Lisa D. ;
Albom, Mark S. ;
Chang, Hong ;
Miknyoczki, Sheila J. ;
Hunter, Kathryn ;
Jones-Bolin, Susan ;
Zhao, Hugh ;
Bacon, Edward R. ;
Mallamo, John P. ;
Ator, Mark A. ;
Ruggeri, Bruce A. .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (02) :903-913