Fasching K, Panzer S, Haas O A, Borkhardt A, Marschalek R, Griesinger F, Panzer-Grümayer E R
Children's Cancer Research Institute, St Anna Kinderspital, and Clinic for Blood Group Serology, University of Vienna, Austria.
Blood. 2001 Oct 1;98(7):2272-4. doi: 10.1182/blood.v98.7.2272.
Childhood acute lymphoblastic leukemia (ALL) is frequently initiated in utero at a time of developmentally regulated insertion of N regions into the DJ(H) rearrangements of immunoglobulin heavy-chain (Ig(H)) genes. Here it is shown that N regions are present in the clonotypic DJ(H) rearrangements in 11 of 12 infant ALLs with t(4;11). These data are compared with the 122 previously published DJ(H) sequences and were found to have a pattern similar to that of ALL in children older than 3 years at diagnosis but were unlike that in children younger than 3 years who predominantly lack N regions. These findings, therefore, indicate that t(4;11)-positive infant ALL is initiated later in fetal development than most B-cell precursor ALL from children younger than 3 years and that they have a shorter latency period already in utero.
儿童急性淋巴细胞白血病(ALL)常于子宫内发育调控期N区域插入免疫球蛋白重链(Ig(H))基因的DJ(H)重排时起始。本文显示,12例t(4;11)的婴儿ALL中,11例克隆型DJ(H)重排存在N区域。将这些数据与之前发表的122个DJ(H)序列进行比较,发现其模式与诊断时年龄大于3岁儿童的ALL相似,但与年龄小于3岁且主要缺乏N区域的儿童ALL不同。因此,这些发现表明,t(4;11)阳性婴儿ALL在胎儿发育中起始时间比大多数3岁以下儿童的B细胞前体ALL更晚,且在子宫内已有更短的潜伏期。