Therapeutic Targets in Malignant Glioblastoma Microenvironment

被引:69
作者
Barcellos-Hoff, Mary Helen [1 ]
Newcomb, Elizabeth W. [1 ]
Zagzag, David [1 ]
narayana, Ashwatha [1 ]
机构
[1] NYU, Langone Sch Med, Dept Radiat Oncol, New York, NY 10016 USA
关键词
GROWTH-FACTOR-BETA; FOCAL ADHESION KINASE; HIGH-GRADE GLIOMA; CHRONIC RADIATION ENTEROPATHY; HYPOXIA-INDUCIBLE FACTOR-1; CENTRAL-NERVOUS-SYSTEM; TGF-BETA; TRANSFORMING GROWTH-FACTOR-BETA-1; IN-VIVO; IONIZING-RADIATION;
D O I
10.1016/j.semradonc.2009.02.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
There is considerable evidence that the tissue microenvironment can suppress cancer and that microenvironment disruption is required for cancer growth and progression. Distortion of the microenvironment by tumor cells can promote growth, recruit nonmalignant cells that provide physiological resources, and facilitate invasion. Compared with the variable routes taken by cells to become cancers, the response of normal tissue to cancer is relatively consistent such that controlling cancer may be more readily achieved indirectly via the microenvironment. Here, we discuss 3 ideas about how the microenvironment, consisting of a vasculature, inflammatory cells, immune cells, growth factors, and extracellular matrix, might provide therapeutic targets in glioblastoma (GBM) in the context of radiotherapy (RT): (1) viable therapeutic targets exist in the GBM microenvironment, (2) RT alters the microenvironment of tissues and tumors; and (3) a potential benefit may be achieved by targeting the microenvironments induced by RT. Semin Radiat Oncol 19:163-170 (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:163 / 170
页数:8
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