Emerging insights into the molecular biology of brain metastases

被引:18
作者
Chen, Guo [1 ]
Davies, Michael A. [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
关键词
Brain metastasis; Blood-brain barrier; Angiogenesis; Targeted therapy; Animal models; Microenvironment; ENDOTHELIAL GROWTH-FACTOR; CELL LUNG-CANCER; BREAST-CANCER; MELANOMA-CELLS; BARRIER PERMEABILITY; PRECLINICAL MODEL; TUMOR PROGRESSION; EXPRESSION; ANGIOGENESIS; CHEMOTHERAPY;
D O I
10.1016/j.bcp.2011.09.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
One of the foremost challenges in oncology is developing improved therapies for preventing and treating metastases to the brain. Recent research in this area is bringing about a shift in the understanding of brain metastases. Previously, the occurrence and poor outcomes associated with brain metastases have been largely attributed to the exclusion of anticancer drugs from the brain by the blood-brain barrier (BBB). However, studies in multiple tumor types have also demonstrated that brain metastases have significant molecular differences from primary tumors and extracranial metastases. These molecular differences may not only promote the formation of brain metastases, but they may also contribute to these tumors' poor responsiveness to therapies. Such changes may be intrinsic to the cancer cells or driven by unique interactions with the brain microenvironment. An improved understanding of the molecular characteristics of brain metastases that contribute to their aggressive behaviors will facilitate the development of rational, more effective treatments for these tumors. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:305 / 314
页数:10
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