Cancer Stem Cells in Pediatric Brain Tumors

被引:18
作者
Lasky, Joseph L., III [1 ,2 ]
Choe, Meeryo [2 ]
Nakano, Ichiro [1 ,2 ]
机构
[1] Ohio State Univ, Dept Neurol Surg, Neural Canc Stem Cell Lab, Columbus, OH 43210 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurosurg & Pediat, Los Angeles, CA 90095 USA
关键词
Brain tumor stem cell; glioma stem cell; medulloblastoma stem cell; brain tumor therapy; CRANIOSPINAL RADIATION-THERAPY; ADJUVANT CHEMOTHERAPY; HEDGEHOG PATHWAY; HUMAN HOMOLOG; PTEN; MEDULLOBLASTOMA; IDENTIFICATION; CHILDREN; LEUKEMIA; GLIOBLASTOMA;
D O I
10.2174/157488809789649278
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Central nervous system (CNS) tumors remain the leading cause of death among pediatric neoplasms. Although standard therapies cure many pediatric CNS tumors, the long-term cognitive and physical consequences of these therapies are devastating. Furthermore, recurrent disease carries a dismal prognosis. Although recent studies have focused on molecular mechanisms that underlie the initiation and progression of adult glioblastoma multiforme (GBM), these tumors differ phenotypically and at a molecular level from pediatric brain tumors. Recent investigations have identified a stem cell population, termed "brain tumor stem cells" (BTSC) within the heterogeneous cell populations that comprise malignant brain tumors which may be partly responsible for the resistance to current therapies. These have been identified in several pediatric tumors including medulloblastoma, ependymomas, and malignant gliomas. By exploiting molecular differences present within these heterogeneous populations of brain tumor cells, we may be able to achieve specific eradication of BTSC and long-lasting remissions, while causing less toxicity to normal tissues. In this review, we describe the issues surrounding the identification and characterization of BTSC, the molecular biology of BTSC for different pediatric brain tumors, and suggest future avenues for the development of treatments for this devastating disease.
引用
收藏
页码:298 / 305
页数:8
相关论文
共 73 条
[21]   Multi-genetic events collaboratively contribute to Pten-null leukaemia stem-cell formation [J].
Guo, Wei ;
Lasky, Joseph L. ;
Chang, Chun-Ju ;
Mosessian, Sherly ;
Lewis, Xiaoman ;
Xiao, Yun ;
Yeh, Jennifer E. ;
Chen, James Y. ;
Iruela-Arispe, M. Luisa ;
Varella-Garcia, Marileila ;
Wu, Hong .
NATURE, 2008, 453 (7194) :529-U7
[22]   Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome [J].
Hahn, H ;
Wicking, C ;
Zaphiropoulos, PG ;
Gailani, MR ;
Shanley, S ;
Chidambaram, A ;
Vorechovsky, I ;
Holmberg, E ;
Unden, AB ;
Gillies, S ;
Negus, K ;
Smyth, I ;
Pressman, C ;
Leffell, DJ ;
Gerrard, B ;
Goldstein, AM ;
Dean, M ;
Toftgard, R ;
ChenevixTrench, G ;
Wainwright, B ;
Bale, AE .
CELL, 1996, 85 (06) :841-851
[23]   PRIMARY BIOASSAY OF HUMAN TUMOR STEM-CELLS [J].
HAMBURGER, AW ;
SALMON, SE .
SCIENCE, 1977, 197 (4302) :461-463
[24]   Diffuse brainstem glioma in children: critical review of clinical trials [J].
Hargrove, D ;
Bartels, U ;
Bouffet, E .
LANCET ONCOLOGY, 2006, 7 (03) :241-248
[25]   Phosphatidylinositol 3′-kinase/AKT signaling is activated in medulloblastoma cell proliferation and is associated with reduced expression of PTEN [J].
Hartmann, Wolfgang ;
Digon-Soentgerath, Boris ;
Koch, Arend ;
Waha, Anke ;
Endl, Elmar ;
Dani, Indra ;
Denkhaus, Dorota ;
Goodyer, Cynthia G. ;
Soerensen, Niels ;
Wiestler, Otmar D. ;
Pietsch, Torsten .
CLINICAL CANCER RESEARCH, 2006, 12 (10) :3019-3027
[26]   Cancerous stem cells can arise from pediatric brain tumors [J].
Hemmati, HD ;
Nakano, I ;
Lazareff, JA ;
Masterman-Smith, M ;
Geschwind, DH ;
Bronner-Fraser, M ;
Kornblum, HI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) :15178-15183
[27]   Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular target [J].
Horvath, S. ;
Zhang, B. ;
Carlson, M. ;
Lu, K. V. ;
Zhu, S. ;
Felciano, R. M. ;
Laurance, M. F. ;
Zhao, W. ;
Qi, S. ;
Chen, Z. ;
Lee, Y. ;
Scheck, A. C. ;
Liau, L. M. ;
Wu, H. ;
Geschwind, D. H. ;
Febbo, P. G. ;
Kornblum, H. I. ;
Cloughesy, T. F. ;
Nelson, S. F. ;
Mischel, P. S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (46) :17402-17407
[28]   Leukaemia stem cells and the evolution of cancer-stem-cell research [J].
Huntly, BJP ;
Gilliland, DG .
NATURE REVIEWS CANCER, 2005, 5 (04) :311-321
[29]  
Inda MD, 2004, ONCOL REP, V12, P1341
[30]   Human homolog of patched, a candidate gene for the basal cell nevus syndrome [J].
Johnson, RL ;
Rothman, AL ;
Xie, JW ;
Goodrich, LV ;
Bare, JW ;
Bonifas, JM ;
Quinn, AG ;
Myers, RM ;
Cox, DR ;
Epstein, EH ;
Scott, MP .
SCIENCE, 1996, 272 (5268) :1668-1671