Andreasson P, Johansson B, Carlsson M, Jarlsfelt I, Fioretos T, Mitelman F, Höglund M
Department of Clinical Genetics, Lund University Hospital, Sweden.
Genes Chromosomes Cancer. 1997 Nov;20(3):299-304.
A BCR/ABL-negative chronic myeloid leukemia (CML) with t(12;14) (p12;q11-13) as the sole chromosomal abnormality was investigated by fluorescence in situ hybridization (FISH), which disclosed a cryptic insertion of ETV6 (previously called TEL), located at 12p12, into ABL at chromosome band 9q34. ETV6/ABL fusion was confirmed by RT-PCR, revealing that the first five exons of ETV6 were fused in frame with ABL at exon 2. Wild-type ETV6 was expressed, in accordance with the FISH results showing no deletion of the second ETV6 allele. ETV6/ABL chimeric transcripts have previously been reported in acute leukemias, but never before in CML. The present case suggests that ETV6/ABL positivity may constitute a new genetic subgroup of BCR-negative CML.
对一例以t(12;14)(p12;q11 - 13)作为唯一染色体异常的BCR/ABL阴性慢性髓性白血病(CML)进行了荧光原位杂交(FISH)研究,结果显示位于12p12的ETV6(以前称为TEL)隐匿插入到9号染色体q34带的ABL基因中。通过逆转录聚合酶链反应(RT-PCR)证实了ETV6/ABL融合,结果显示ETV6的前五个外显子与ABL基因的第2外显子框内融合。野生型ETV6表达,这与FISH结果显示第二个ETV6等位基因未缺失相符。ETV6/ABL嵌合转录本以前在急性白血病中已有报道,但在CML中从未有过报道。本病例提示ETV6/ABL阳性可能构成BCR阴性CML的一个新的遗传亚组。