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Progress on Potential Strategies to Target Brain Tumor Stem Cells

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Publisher Springer
Date 2008 Sep 11
PMID 18781384
Citations 7
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Abstract

The identification of brain tumor stem cells (BTSCs) leads to promising progress on brain tumor treatment. For some brain tumors, BTSCs are the driving force of tumor growth and the culprits that make tumor revive and resistant to radiotherapy and chemotherapy. Therefore, it is specifically significant to eliminate BTSCs for treatment of brain tumors. There are considerable similarities between BTSCs and normal neural stem cells (NSCs), and diverse aspects of BTSCs have been studied to find potential targets that can be manipulated to specifically eradicate BTSCs without damaging normal NSCs, including their surface makers, surrounding niche, and aberrant signaling pathways. Many strategies have been designed to kill BTSCs, and some of them have reached, or are approaching, effective therapeutic results. Here, we will focus on advantages in the issue of BTSCs and emphasize on potential therapeutic strategies targeting BTSCs.

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References
1.
Bao S, Wu Q, Sathornsumetee S, Hao Y, Li Z, Hjelmeland A . Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor. Cancer Res. 2006; 66(16):7843-8. DOI: 10.1158/0008-5472.CAN-06-1010. View

2.
Vescovi A, Galli R, Reynolds B . Brain tumour stem cells. Nat Rev Cancer. 2006; 6(6):425-36. DOI: 10.1038/nrc1889. View

3.
Bruggeman S, Hulsman D, Tanger E, Buckle T, Blom M, Zevenhoven J . Bmi1 controls tumor development in an Ink4a/Arf-independent manner in a mouse model for glioma. Cancer Cell. 2007; 12(4):328-41. DOI: 10.1016/j.ccr.2007.08.032. View

4.
Moore K, Lemischka I . Stem cells and their niches. Science. 2006; 311(5769):1880-5. DOI: 10.1126/science.1110542. View

5.
Bao S, Wu Q, McLendon R, Hao Y, Shi Q, Hjelmeland A . Glioma stem cells promote radioresistance by preferential activation of the DNA damage response. Nature. 2006; 444(7120):756-60. DOI: 10.1038/nature05236. View