Glioblastoma Multiforme Therapy and Mechanisms of Resistance

被引:184
|
作者
Ramirez, Yulian P. [1 ,2 ]
Weatherbee, Jessica L. [1 ,2 ]
Wheelhouse, Richard T. [3 ]
Ross, Alonzo H. [1 ,2 ]
机构
[1] Univ Massachusetts, Med Sch, Dept Biochem & Mol Pharmacol, 364 Plantat St, Worcester, MA 01605 USA
[2] Univ Massachusetts, Med Sch, Dept Canc Biol, Worcester, MA 01605 USA
[3] Univ Bradford, Sch Pharm, Bradford BD7 1DP, W Yorkshire, England
来源
PHARMACEUTICALS | 2013年 / 6卷 / 12期
基金
美国国家卫生研究院;
关键词
angiogenesis; autophagy; imidazotetrazine; MGMT; DNA repair; temozolomide; cancer stem cells;
D O I
10.3390/ph6121475
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glioblastoma multiforme (GBM) is a grade IV brain tumor characterized by a heterogeneous population of cells that are highly infiltrative, angiogenic and resistant to chemotherapy. The current standard of care, comprised of surgical resection followed by radiation and the chemotherapeutic agent temozolomide, only provides patients with a 12-14 month survival period post-diagnosis. Long-term survival for GBM patients remains uncommon as cells with intrinsic or acquired resistance to treatment repopulate the tumor. In this review we will describe the mechanisms of resistance, and how they may be overcome to improve the survival of GBM patients by implementing novel chemotherapy drugs, new drug combinations and new approaches relating to DNA damage, angiogenesis and autophagy.
引用
收藏
页码:1475 / 1506
页数:32
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