Zhou Fen, Mei Heng, Jin Runming, Li Xiaoqing, Chen Xiangjun
Department of Pediatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.
J Pediatr Hematol Oncol. 2011 Aug;33(6):429-32. doi: 10.1097/MPH.0b013e318217f5f2.
Ikaros is a zinc-finger transcription factor that plays an important role in the differentiation and proliferation of lymphocytes. Dominant-negative Ikaros isoform 6 (Ik6), one of its common subtypes, is overexpressed in leukemia patients and is associated with unfavorable prognosis in childhood B-cell progenitor acute lymphoblastic leukemia (ALL). This study was to identify specific isoforms, especially Ik6, in Chinese pediatric patients with ALL. The mRNA expression of Ikaros was detected in 88 children with previously untreated ALL by nested reverse transcription-polymerase chain reaction (RT-PCR). Sequencing of the PCR products was performed to identify specific isoforms. The expression of fusion genes was determined by using multiplex RT-PCR. The functional isoforms Ik1, Ik2/3, and dominant negative isoforms Ik4, 6, 8, 9, 10 identified by nested RT-PCR were further confirmed by sequence analysis. In the 88 cases, the Ik6 was found to be overexpressed in 8 of 70 cases of B-lineage ALL and in 1 of 18 cases of T-lineage ALL patients. Among Ik6 B-lineage ALL patients, 3 had expression of BCR/ABL fusion gene and 1 had HOX11 expression. Ik6 overexpression was independent of age, white blood cell count at diagnosis, risk group, and expression of the fusion genes currently measured in China except BCR/ABL (P<0.01). And it was strongly associated with elevated levels of minimal residual disease at day 28 (P<0.01). Ik6 can be included as a high-risk factor at diagnosis. In developing countries with limited resources, it can be economically detected by nested RT-PCR.
伊卡洛斯是一种锌指转录因子,在淋巴细胞的分化和增殖中发挥重要作用。其常见亚型之一显性负性伊卡洛斯异构体6(Ik6)在白血病患者中过度表达,且与儿童B细胞祖细胞急性淋巴细胞白血病(ALL)的不良预后相关。本研究旨在鉴定中国儿童ALL患者中的特定异构体,尤其是Ik6。通过巢式逆转录-聚合酶链反应(RT-PCR)检测了88例未经治疗的ALL患儿伊卡洛斯的mRNA表达。对PCR产物进行测序以鉴定特定异构体。使用多重RT-PCR测定融合基因的表达。通过序列分析进一步证实了巢式RT-PCR鉴定的功能性异构体Ik1、Ik2/3以及显性负性异构体Ik4、6、8、9、10。在这88例病例中,发现Ik6在70例B系ALL患者中的8例以及18例T系ALL患者中的1例中过度表达。在Ik6 B系ALL患者中,3例有BCR/ABL融合基因表达,1例有HOX11表达。Ik6过度表达独立于年龄、诊断时的白细胞计数、风险组以及目前在中国检测的除BCR/ABL外的融合基因表达(P<0.01)。并且它与第28天微小残留病水平升高密切相关(P<0.01)。Ik6可作为诊断时的一个高危因素。在资源有限的发展中国家,可通过巢式RT-PCR进行经济检测。