Salomon-Nguyen F, Brizard F, Le Coniat M, Radford I, Berger R, Brizard A
INSERM U 301 and SD401 No. 301 CNRS, Paris, France.
Leukemia. 1998 Jun;12(6):972-5. doi: 10.1038/sj.leu.2401034.
Abnormalities of the short arm of chromosome 12 are nonrandom events in T cell prolymphocytic leukemia (T-PLL). Fluorescence in situ hybridization (FISH) studies were performed in three patients with T-PLL and one patient with T cell peripheral lymphoma and rearrangement of 12p. Whereas the rearrangements of 12p were different in the four patients, a breakpoint centromeric to the ETV6 gene was present in the three T-PLL patients. In addition, loss of heterozygosity for a chromosomal segment telomeric to ETV6 with loss of the RAD52 locus was also shown by FISH studies. In contrast, the breakpoint was telomeric to ETV6 in the patient with peripheral lymphoma.
12号染色体短臂异常是T细胞幼淋巴细胞白血病(T-PLL)中的非随机事件。对3例T-PLL患者和1例伴有12p重排的T细胞外周淋巴瘤患者进行了荧光原位杂交(FISH)研究。虽然4例患者的12p重排不同,但3例T-PLL患者中均存在一个位于ETV6基因着丝粒侧的断点。此外,FISH研究还显示,与ETV6基因端粒侧的一个染色体片段存在杂合性缺失,且RAD52基因座缺失。相比之下,外周淋巴瘤患者的断点位于ETV6基因的端粒侧。