Sasaki M S
Gan To Kagaku Ryoho. 1986 Mar;13(3 Pt 2):645-51.
An absence of gene(s) on the Rb locus of chromosome 13 or a disturbance of its normal expression in the retinoblasts of the embryonic retina predisposes an individual to the development of retinoblastoma. Chromosome aberrations involving 13q14 comprised about 14% of newly arising germinal mutations. Chromosome analysis of retinoblastoma tumor cells revealed that the generation of an extra copy of the long arm of chromosome 1 or the short arm of chromosome 6 is an early event in many of the tumors and plays a significant role in engendering tumorigenicity of retinoblasts already having one mutation at the Rb locus.
13号染色体Rb基因座上基因的缺失或胚胎视网膜成视网膜细胞中其正常表达的紊乱使个体易患视网膜母细胞瘤。涉及13q14的染色体畸变约占新发生的生殖细胞突变的14%。视网膜母细胞瘤肿瘤细胞的染色体分析显示,1号染色体长臂或6号染色体短臂额外拷贝的产生是许多肿瘤中的早期事件,并且在已经在Rb基因座发生一个突变的成视网膜细胞的致瘤性产生中起重要作用。