儿童急性淋巴细胞白血病SOCS3 mRNA的表达水平与临床特点、早期治疗反应的相关性
[Abstract]:Objective: to observe the expression of cytokine signal transduction inhibitor 3 (SOCS3 mRNA) in (ALL) of childhood acute lymphoblastic leukemia (AML), and to analyze the relationship between the expression of SOCS3 mRNA and the disease status and risk of ALL in children. To explore the application of SOCS3 mRNA in the assessment of disease status and risk of ALL in children. Methods: the expression of SOCS3 mRNA in bone marrow mononuclear cells of 45 newly diagnosed ALL children and 13 normal children was detected by SYBR Green fluorescence quantitative PCR. ANOVA and rank sum test were used to analyze the relationship between SOCS3 mRNA expression level and ALL risk and clinical characteristics. Immunofluorescence histochemical staining and laser confocal microscopy were used to detect the location and expression of SOCS3 mRNA in bone marrow monocytes of children with ALL. Results: the expression of SOCS3mRNA in 45 children was significantly lower than that in normal children (P0.05), but there was no significant difference in SOCS3 mRNA expression between 45 children and normal children (P0.05). In the first visit, the expression of SOCS3 mRNA in high risk group was higher than that in low risk group (P0.05). According to the median method, 45 children were divided into high expression group and low expression group according to the median method. Comparing the clinical characteristics of the two groups, it was found that the high expression group of SOCS3 mRNA had higher peripheral blood leukocyte count. Lactate dehydrogenase level and poor prognosis gene. In addition, the risk of high expression of SOCS3 mRNA was higher in the two groups than in the risk group. Conclusion: SOCS3 mRNA is down-regulated at first visit and returns to normal expression after disease induction and remission. SOCS3 can be used as an index to evaluate the disease state. The high expression of SOCS3 mRNA can increase the risk of ALL, and SOCS3 mRNA can be used as a risk factor to evaluate the risk of ALL. The treatment of ALL by regulating the level of SOCS3 mRNA expression may be a new direction of treatment.
【作者单位】: 安徽医科大学第二附属医院儿科;
【分类号】:R733.71
【相似文献】
相关期刊论文 前2条
1 邹宁;李晓环;刘正娟;;SOCS3与瘦素抵抗[J];中国妇幼保健;2009年11期
2 王琳;徐建波;吴河水;张进祥;田元;;脐血单个核细胞TLR及SOCS mRNA的表达及意义[J];中国妇幼保健;2006年10期
相关会议论文 前2条
1 王国兵;李成荣;杨军;温鹏强;贾实磊;;SOCS1/SOCS3甲基化改变在儿童急性ITP Th17/Treg细胞失衡中的作用初探[A];中华医学会第十七次全国儿科学术大会论文汇编(上册)[C];2012年
2 夏倩;胡成平;秦岭;;SOCS3和SOCS5在RSV感染支气管上皮细胞的TH1/TH2免疫失衡中的表达[A];中华医学会呼吸病学年会——2011(第十二次全国呼吸病学学术会议)论文汇编[C];2011年
相关博士学位论文 前1条
1 顾强;SOCS3调控JAK2/STAT3信号通路在心肌慢性缺氧适应中意义的研究[D];第三军医大学;2011年
相关硕士学位论文 前5条
1 訾广芹;过敏性紫癜儿童SOCS表达及与Th17/Treg细胞失衡关系研究[D];青岛大学;2015年
2 张庆群;SOCS低甲基化在过敏性紫癜儿童Th17/Treg细胞失衡中的作用研究[D];青岛大学;2015年
3 廖立夏;SOCS1、SOCS3在过敏性紫癜儿童Th1/Th2失衡中的作用探讨[D];青岛大学;2016年
4 曾晓红;SOCS-1、SOCS-3在过敏性紫癜患儿Th1/Th2、Th17/Treg细胞失衡中的作用[D];西南医科大学;2016年
5 冯泽洲;紫绀型先心病患儿心肌SOCS3启动子甲基化分析及可能机制研究[D];第三军医大学;2014年
,本文编号:2301159
本文链接:https://www.wllwen.com/yixuelunwen/eklw/2301159.html