Targeting the Tumor Stroma in Cancer Therapy

被引:29
|
作者
Anton, Kevin [2 ]
Glod, John [1 ,2 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Canc Inst New Jersey, Dept Pediat Oncol, New Brunswick, NJ 08903 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Canc Inst New Jersey, Dept Pharmacol, New Brunswick, NJ 08903 USA
关键词
MESENCHYMAL STEM-CELLS; ENDOTHELIAL GROWTH-FACTOR; METALLOPROTEINASE INHIBITOR PRINOMASTAT; PLASMINOGEN-ACTIVATOR SYSTEM; TYROSINE KINASE INHIBITOR; ACUTE MYELOID-LEUKEMIA; BREAST-CANCER; PHASE-II; MACROPHAGE INFILTRATION; PROTEIN-ALPHA;
D O I
10.2174/138920109787315088
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
Increasing evidence shows that the interaction between neoplastic cells and the surrounding stroma is a critical factor in solid tumor growth. The tumor stroma is made up of diverse cellular populations including macrophages, lymphocytes, vascular cells, and carcinoma-associated fibroblasts. The complex interactions between the stroma and neoplastic cells are largely unexplored. Initial therapies aimed at disrupting angiogenesis within the tumor microenvironment have met with success in a number of tumor types. An improved understanding of stromal signaling pathways is likely to identify additional novel therapeutic targets.
引用
收藏
页码:185 / 191
页数:7
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