The search for the retinoblastoma cell of origin

被引:118
作者
Dyer, MA
Bremner, R
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
[2] Univ Hlth Network, Toronto Western Res Inst, Toronto, ON M5T 2S8, Canada
[3] Univ Toronto, Vis Sci Res Program, Lab Med & Pathobiol, Dept Ophthalmol, Toronto, ON M5T 2S8, Canada
[4] Univ Toronto, Vis Sci Res Program, Lab Med & Pathobiol, Dept Visual Sci, Toronto, ON M5T 2S8, Canada
基金
加拿大健康研究院; 美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1038/nrc1545
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The cellular effects of the genetic defects associated with tumorigenesis are context dependent. To better understand the reasons that different cell types require distinct combinations of mutations to form tumours, it is essential to identify and characterize a tumour's 'cell of origin'. Retinoblastoma, a rare childhood cancer of the retina that is caused by RB inactivation, is a good model in which to search for a tumour cell of origin, because retinal development is well understood and the initiating genetic lesion is well characterized. Identifying the cell of origin for this tumour would advance our understanding of how cellular context affects the requirement of specific mutations for cancer initiation and progression.
引用
收藏
页码:91 / 101
页数:11
相关论文
共 80 条
[1]  
Alexiades MR, 1997, DEVELOPMENT, V124, P1119
[2]   THE AGE DISTRIBUTION OF CANCER AND A MULTI-STAGE THEORY OF CARCINOGENESIS [J].
ARMITAGE, P ;
DOLL, R .
BRITISH JOURNAL OF CANCER, 1954, 8 (01) :1-12
[3]  
BeleckyAdams T, 1997, INVEST OPHTH VIS SCI, V38, P1293
[4]  
Belliveau MJ, 1999, DEVELOPMENT, V126, P555
[5]  
Belliveau MJ, 2000, J NEUROSCI, V20, P2247
[6]   MicroSAGE is highly representative and reproducible but reveals major differences in gene expression among samples obtained from similar tissues [J].
Blackshaw, S ;
Kuo, WP ;
Park, PJ ;
Tsujikawa, M ;
Gunnersen, JM ;
Scott, HS ;
Boon, WM ;
Tan, SS ;
Cepko, CL .
GENOME BIOLOGY, 2003, 4 (03)
[7]   Genomic analysis of mouse retinal development [J].
Blackshaw, S ;
Harpavat, S ;
Trimarchi, J ;
Cai, L ;
Huang, HY ;
Kuo, WP ;
Weber, G ;
Lee, K ;
Fraioli, RE ;
Cho, SH ;
Yung, R ;
Asch, E ;
Ohno-Machado, L ;
Wong, WH ;
Cepko, CL .
PLOS BIOLOGY, 2004, 2 (09) :1411-1431
[8]   Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes [J].
Blackshaw, S ;
Fraioli, RE ;
Furukawa, T ;
Cepko, CL .
CELL, 2001, 107 (05) :579-589
[9]   INDUCTION OF DIFFERENT GENETIC CHANGES BY DIFFERENT CLASSES OF CHEMICAL CARCINOGENS DURING PROGRESSION OF MOUSE SKIN TUMORS [J].
BREMNER, R ;
KEMP, CJ ;
BALMAIN, A .
MOLECULAR CARCINOGENESIS, 1994, 11 (02) :90-97
[10]   GENETIC CHANGES IN SKIN TUMOR PROGRESSION - CORRELATION BETWEEN PRESENCE OF A MUTANT RAS GENE AND LOSS OF HETEROZYGOSITY ON MOUSE CHROMOSOME-7 [J].
BREMNER, R ;
BALMAIN, A .
CELL, 1990, 61 (03) :407-417