Targeting the Tumor Microenvironment: From Understanding Pathways to Effective Clinical Trials

被引:260
作者
Fang, Hua [1 ,5 ]
DeClerck, Yves A. [1 ,2 ,3 ,4 ]
机构
[1] Univ So Calif, Div Hematol Oncol, Los Angeles, CA USA
[2] Univ So Calif, Dept Pediat, Los Angeles, CA 90089 USA
[3] Univ So Calif, Dept Biochem & Mol Biol, Los Angeles, CA USA
[4] Childrens Hosp Los Angeles, Saban Res Inst, Los Angeles, CA 90027 USA
[5] Univ Chicago, Dept Med, Comm Clin Pharmacol & Pharmacogen, Chicago, IL 60637 USA
关键词
TYROSINE KINASE INHIBITOR; NECROSIS-FACTOR-ALPHA; NF-KAPPA-B; HYPOXIA-ACTIVATED PRODRUG; ENDOTHELIAL GROWTH-FACTOR; RANDOMIZED PHASE-II; SILTUXIMAB CNTO 328; MONOCLONAL-ANTIBODY; BREAST-CANCER; TGF-BETA;
D O I
10.1158/0008-5472.CAN-13-0661
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
It is clear that tumor cells do not act alone but in close interaction with the extracellular matrix and with stromal cells in the tumor microenvironment (TME). As our understanding of tumor cell-stroma interactions increased over the last two decades, significant efforts have been made to develop agents that interfere with these interactions. Here, we discuss four different therapeutic strategies that target the TME, focusing on agents that are at the most advanced stage of preclinical or clinical development. We end this review by outlining some of the lessons we have learned so far from the development of TME-targeting agents. (C) 2013 AACR.
引用
收藏
页码:4965 / 4977
页数:13
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