Brain tumor stem cells: Bringing order to the chaos of brain cancer

被引:120
作者
Dirks, Peter B. [1 ]
机构
[1] Univ Toronto, Hosp Sick Children, Arthur & Sonia Labatt Brain Tumor Res Ctr, Program Dev & Stem Cell Biol, Toronto, ON M5G 1X5, Canada
关键词
D O I
10.1200/JCO.2008.17.6792
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Brain tumors are generally incurable cancers. Work from a number of laboratories strongly suggests that they are organized as a hierarchy based on a subset of cancer cells that have stem-cell properties. These cells have now been shown to be resistant to conventional therapy and responsive to differentiation therapy. New in vitro and in vivo models for interrogating brain tumor cells in stem-cell conditions have been developed that provide important new opportunities for elucidating the key pathways responsible for driving the proliferation of these cells. Continued application of the principles of stem-cell biology to the study of brain cancers is likely to continue to bring further important insight into these aggressive cancers, bringing new treatments and understanding of the origins.
引用
收藏
页码:2916 / 2924
页数:9
相关论文
共 112 条
[1]   Gli and hedgehog in cancer:: Tumours, embryos and stem cells [J].
Altaba, AR ;
Sánchez, P ;
Dahmane, N .
NATURE REVIEWS CANCER, 2002, 2 (05) :361-372
[2]   AUTORADIOGRAPHIC INVESTIGATION OF CELL PROLIFERATION IN BRAINS OF RATS AND CATS [J].
ALTMAN, J .
ANATOMICAL RECORD, 1963, 145 (04) :573-&
[3]   HOXB4 overexpression mediates very rapid stem cell regeneration and competitive hematopoietic repopulation [J].
Antonchuk, J ;
Sauvageau, G ;
Humphries, RK .
EXPERIMENTAL HEMATOLOGY, 2001, 29 (09) :1125-1134
[4]   Epidermal growth factor receptor and Ink4a/Arf:: Convergent mechanisms governing terminal differentiation and transformation along the neural stem cell to astrocyte axis [J].
Bachoo, RM ;
Maher, EA ;
Ligon, KL ;
Sharpless, NE ;
Chan, SS ;
You, MJJ ;
Tang, Y ;
DeFrances, J ;
Stover, E ;
Weissleder, R ;
Rowitch, DH ;
Louis, DN ;
DePinho, RA .
CANCER CELL, 2002, 1 (03) :269-277
[5]   Glioma stem cells promote radioresistance by preferential activation of the DNA damage response [J].
Bao, Shideng ;
Wu, Qiulian ;
McLendon, Roger E. ;
Hao, Yueling ;
Shi, Qing ;
Hjelmeland, Anita B. ;
Dewhirst, Mark W. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
NATURE, 2006, 444 (7120) :756-760
[6]   Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor [J].
Bao, Shideng ;
Wu, Qiulian ;
Sathornsumetee, Sith ;
Hao, Yueling ;
Li, Zhizhong ;
Hjelmeland, Anita B. ;
Shi, Oing ;
McLendon, Roger E. ;
Bigner, Darell D. ;
Rich, Jeremy N. .
CANCER RESEARCH, 2006, 66 (16) :7843-7848
[7]   Cyclopamine-mediated hedgehog pathway inhibition depletes stem-like cancer cells in glioblastoma [J].
Bar, Eli E. ;
Chaudhry, Aneeka ;
Lin, Alex ;
Fan, Xing ;
Schreck, Karisa ;
Matsui, William ;
Piccirillo, Sara ;
Vescovi, Angelo L. ;
DiMeco, Francesco ;
Olivi, Alessandro ;
Eberharta, Charles G. .
STEM CELLS, 2007, 25 (10) :2524-2533
[8]   Tissue repair and stem cell renewal in carcinogenesis [J].
Beachy, PA ;
Karhadkar, SS ;
Berman, DM .
NATURE, 2004, 432 (7015) :324-331
[9]   CD133+ and CD133- glioblastoma-derived cancer stem cells show differential growth characteristics and molecular profiles [J].
Beier, Dagmar ;
Hau, Peter ;
Proescholdt, Martin ;
Lohmeier, Annette ;
Wischhusen, Joerg ;
Oefner, Peter J. ;
Aigner, Ludwig ;
Brawanski, Alexander ;
Bogdahn, Ulrich ;
Beier, Christoph P. .
CANCER RESEARCH, 2007, 67 (09) :4010-4015
[10]   Daoy medulloblastoma cells that express CD133 are radioresistant relative to CD133- cells, and the CD133+ sector is enlarged by hypoxia [J].
Blazek, Ed R. ;
Foutch, Jennifer L. ;
Maki, Guitta .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2007, 67 (01) :1-5