Zhang Xiao-Hui, Luo Jian-Min, Yang Lin, Liu Xiao-Jun
Department of Hematology, Handan Central Hospital of Hebei Province, Handan 056001, Hebei Province, China,E-mail:
Department of Hematology, The Second Hospital of Hebei Medical University, Shijiazhuang 050000, Hebei Province, China,E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Oct;28(5):1496-1503. doi: 10.19746/j.cnki.issn.1009-2137.2020.05.012.
To explore the correlation of SOCS1 gene methylation with the activity of JAK2/STAT signaling pathway, genesis and progress of acute myeloid leukemia.
Several techniques, such as cell culture, qPCR, MS-PCR, Western bolt, CCK-8 assay, flow cytometry and gene transfection were used to analyze the relation of expression and methylation statues of SOCS1 gene with the genesis and progression of AML in 120 AML patients and leukemia cell lines U937 and THP-1, at the same time to analyze the changes of downstream protein expression in JAK2/STAT signaling pathway and their effect on the growth and apoptosis of leukemia cell lines.
The positive rate of WT1/ABL in SOCS1 methylated group was significantly higher than that in SOCS1 non-methylated group, and the complete remission rate of one course treatment in SOCS1-methylated group was significantly lower than that in SOCS1 non-methylated group. The expression level of SOCS1 gene in low methylation rate group was higher, and the expression of down-stream proteins p-JAK2, p-STAT3 and p-STAT5 in JAK2/STAT signaling pathway decreased, while the expression of t-JAK2,t-STAT3 and t-STAT5 was not changed statistically significantly. The growth rate of leukemia cells graduated decreased, and the apoptosis rate of leukemia cells graduated increased along with the enhancement of methylation drug concentration.
The methylation of SOCS1 gene results in the gene silencing, thereby declines its inhibition on the down-stream proteins in JAK2/STAT signaling pathway, and finally promotes the growth and proliferation of AML cells.
探讨SOCS1基因甲基化与JAK2/STAT信号通路活性、急性髓系白血病发生发展的相关性。
采用细胞培养、qPCR、MS-PCR、Western bolt、CCK-8检测、流式细胞术及基因转染等技术,分析120例急性髓系白血病患者及白血病细胞株U937和THP-1中SOCS1基因表达及甲基化状态与急性髓系白血病发生发展的关系,同时分析JAK2/STAT信号通路下游蛋白表达变化及其对白血病细胞株生长和凋亡的影响。
SOCS1甲基化组WT1/ABL阳性率显著高于SOCS1非甲基化组,SOCS1甲基化组一疗程治疗完全缓解率显著低于SOCS1非甲基化组。低甲基化率组SOCS1基因表达水平较高,JAK2/STAT信号通路下游蛋白p-JAK2、p-STAT3和p-STAT5表达降低,而t-JAK2、t-STAT3和t-STAT5表达无统计学显著变化。随着甲基化药物浓度升高,白血病细胞生长率逐渐降低,凋亡率逐渐升高。
SOCS1基因甲基化导致基因沉默,从而减弱其对JAK2/STAT信号通路下游蛋白的抑制作用,最终促进急性髓系白血病细胞的生长和增殖。