Clinical significance of WT1 gene expression in peripheral blood cells and bone marrow cells of childhood leukemia

Xiao-ling Bai, H. Zhao, Hui Yao, Nan Zheng, Bo Xu, Nianzheng Sun, G. Jiang, T. Tang
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Abstract

Objective To set up a simple, quick and accurate method for monitoring minimal residual disease (MRD) of leukemia, the clinical significance of WT1 gene expression in peripheral blood (PB) cells was compared with that in bone marrow (BM) cells from children with the acute leukemia (AL). Methods Thirty-four children with AL were selected in this study, including 23 acute lymphoblastic leukemia (ALL) and 11 acute myeloid leukemia (AML). Normal PB cells from 8 healthy children and BM cells from 8 non-hematological disease patients were used as the negative control and K562 cells as the positive control. Relative levels of WT1 gene expression in PB and BM mononuclear cells from 34 AL were dynamically detected by using the nested reverse transcriptase-polymerase chain reaction (RT-PCR), and analyzed quantitatively with GQS-960 image processing system software. The WT1/β-actin ratio was calculated. Results (1) WT1 gene expression showed 0.784±0.311 in BM cells of 27 patients with recently diagnosis, and 0.734±0.295 in PB cells of 26 cases. There was no difference of the WT1 gene expression(P>0.05). (2) Twenty-six out of 32 cases with AL achieved complete remission (CR) after chemotherapy, including 20 cases with WT1 positive expression in BM and PB, 6 cases with WT1 negative expression. The CR rate showed no difference. (3) Relative levels of WT1 gene expression in PB and BM markedly decreased after CR, 12 of 20 cases with WT1+ in BM changed to negative expression of WT1 gene. Eight cases still lasted positive (0.376±0.162 ). Fifteen of 20 cases with WT1+ in PB changed to negative expression, 8 cases still lasted positive (0.229±0.105 ). Six NR patients showed continued positive expression of WT1 gene (0.912±0.241 ). (4) Eighteen patients with WT1+ at the diagnosis were followed up from 6 to 24 months. Five out of 8 cases of WT1+ in BM relapsed, 3 out of 10 cases WT1- relapsed, which showed no market difference. While 5 cases with WT1+ in PB were all relapse, 3 out of 13 cases with WT1- relapsed, which showed significant difference (P=0.006 5). Conclusion The dynamic analysis of WT1 gene expression in children with AL could be used to monitor MRD and predict early relapse. WT1 gene expression detected in PB cells of MRD seems to be more specific and convenient than that detected in BM cells. Key words: Leukemia; Neoplasm residual; Oncogenes; Gene expression; Polymerase chain reaction
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WT1基因在儿童白血病外周血和骨髓细胞表达的临床意义
目的建立一种简便、快速、准确的白血病微小残留病(MRD)监测方法,比较急性白血病(AL)患儿外周血(PB)细胞WT1基因与骨髓(BM)细胞WT1基因表达的临床意义。方法选择急性淋巴细胞白血病(ALL)患儿23例,急性髓系白血病(AML)患儿11例,共34例。以8例健康儿童的正常PB细胞和8例非血液病患者的BM细胞为阴性对照,K562细胞为阳性对照。采用巢式逆转录-聚合酶链式反应(RT-PCR)动态检测34例AL中PB和BM单核细胞中WT1基因的相对表达水平,并用GQS-960图像处理系统软件进行定量分析。计算WT1/β-actin比值。结果(1)WT1基因在27例初诊患者BM细胞中表达0.784±0.311,在26例PB细胞中表达0.734±0.295。各组WT1基因表达量差异无统计学意义(P>0.05)。(2) 32例AL患者化疗后完全缓解(CR) 26例,其中BM和PB WT1阳性表达20例,WT1阴性表达6例。CR率无显著差异。(3) CR后PB和BM中WT1基因的相对表达水平明显降低,BM中WT1+的20例中有12例变为WT1基因的负表达。8例仍持续阳性(0.376±0.162)。20例PB中WT1+阳性15例转为阴性表达,8例仍维持阳性(0.229±0.105)。6例NR患者WT1基因持续阳性表达(0.912±0.241)。(4)对18例确诊时WT1+的患者进行6 ~ 24个月的随访。BM患者WT1+复发8例中5例,WT1-复发10例中3例,无市场差异。PB中WT1+患者5例全部复发,WT1-患者13例中有3例复发,差异有统计学意义(P= 0.0065)。结论动态分析AL患儿WT1基因表达可用于监测MRD,预测早期复发。在MRD的PB细胞中检测WT1基因表达似乎比在BM细胞中检测更特异性和方便。关键词:白血病;肿瘤残留;致癌基因;基因表达;聚合酶链反应
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