Mouse models of childhood cancer of the nervous system

被引:42
作者
Dyer, MA [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
关键词
D O I
10.1136/jcp.2003.009910
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Targeted cancer treatments rely on understanding signalling cascades, genetic changes, and compensatory programmes activated during tumorigenesis. Increasingly, pathologists are required to interpret molecular profiles of tumour specimens to target new treatments. This is challenging because cancer is a heterogeneous disease tumours change over time in individual patients and genetic lesions leading from preneoplasia to malignancy can differ substantially between patients. For childhood tumours of the nervous system, the challenge is even greater, because tumours arise from progenitor cells in a developmental context different from that of the adult, and the cells of origin, neural progenitor cells, show considerable temporal and spatial heterogeneity during development. Thus, the underlying mechanisms regulating normal development of the nervous system also need to be understood. Many important advances have come from model mouse genetic systems. This review will describe several mouse models of childhood tumours of the nervous system, emphasising how understanding the normal developmental processes, combined with mouse models of cancer and the molecular pathology of the human diseases, can provide the information needed to treat cancer more effectively.
引用
收藏
页码:561 / 576
页数:16
相关论文
共 104 条
[81]   Neuroblastoma screening at one year of age [J].
Schilling, FH ;
Spix, C ;
Berthold, F ;
Erttmann, R ;
Fehse, N ;
Hero, B ;
Klein, G ;
Sander, J ;
Schwarz, K ;
Treuner, J ;
Zorn, U ;
Michaelis, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (14) :1047-1053
[82]   Biologic factors determine prognosis in infants with stage IV neuroblastoma: A prospective Children's Cancer Group study [J].
Schmidt, ML ;
Lukens, JN ;
Seeger, RC ;
Brodeur, GM ;
Shimada, H ;
Gerbing, RB ;
Stram, DO ;
Perez, C ;
Haase, GM ;
Matthay, KK .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (06) :1260-1268
[83]   AMPLIFIED DNA WITH LIMITED HOMOLOGY TO MYC CELLULAR ONCOGENE IS SHARED BY HUMAN NEURO-BLASTOMA CELL-LINES AND A NEURO-BLASTOMA TUMOR [J].
SCHWAB, M ;
ALITALO, K ;
KLEMPNAUER, KH ;
VARMUS, HE ;
BISHOP, JM ;
GILBERT, F ;
BRODEUR, G ;
GOLDSTEIN, M ;
TRENT, J .
NATURE, 1983, 305 (5931) :245-248
[84]   ORIGINS OF NEURAL CREST CELL DIVERSITY [J].
SELLECK, MAJ ;
SCHERSON, TY ;
BRONNERFRASER, M .
DEVELOPMENTAL BIOLOGY, 1993, 159 (01) :1-11
[85]   Context-dependent regulation of fate decisions in multipotent progenitor cells of the peripheral nervous system [J].
Sommer, L .
CELL AND TISSUE RESEARCH, 2001, 305 (02) :211-216
[86]  
Sterling-Levis K, 2003, IN VIVO, V17, P329
[87]   Engraftment of sorted/expanded human central nervous system stem cells from fetal brain [J].
Tamaki, S ;
Eckert, K ;
He, DP ;
Sutton, R ;
Doshe, M ;
Jain, G ;
Tushinski, R ;
Reitsma, M ;
Harris, B ;
Tsukamoto, A ;
Gage, F ;
Weissman, I ;
Uchida, N .
JOURNAL OF NEUROSCIENCE RESEARCH, 2002, 69 (06) :976-986
[88]  
TANAKA T, 1988, CANCER RES, V48, P1030
[89]   Molecular insight into medulloblastoma and central nervous system primitive neuroectodermal tumor biology from hereditary syndromes: A review [J].
Taylor, MD ;
Mainprize, TG ;
Rutka, JT .
NEUROSURGERY, 2000, 47 (04) :888-901
[90]   Null mutation of DNA strand break-binding molecule poly(ADP-ribose) polymerase causes medulloblastomas in p53-/- mice [J].
Tong, WM ;
Ohgaki, H ;
Huang, HT ;
Granier, C ;
Kleihues, P ;
Wang, ZQ .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (01) :343-352