miR-181a-3p通过靶向SOCS5抑制急性淋巴细胞白血病细胞恶性进展OA
miR-181a-3p Inhibits Malignant Progression of Acute Lymphoblastic Leukemia Cells by Targeting SOCS5
目的 探究微小RNA(microRNA,miRNA)-181 a-3 p通过靶向调控细胞因子信号传导抑制因子5(suppressor of cytokine signaling 5,SOCS5)对急性淋巴细胞白血病(acute lymphoblastic leukemia,ALL)细胞恶性进展.方法 实时荧光定量 PCR(RT-qPCR)和蛋白质印迹法检测 ALL 细胞中 miR-181a-3p、SOCS5 表达水平.MoIt4 细胞分为 anti-miR-181a-3p 组、anti-miR-NC 组、pcDNA 组、anti-miR-181a-3p+si-NC组、pcDNA-SOCS5 组、anti-miR-181a-3p+si-SOCS5 组.RT-qPCR检测 miR-181a-3p、SOCS5 表达水平,细胞计数试剂盒(CCK8)和Transwell检测细胞增殖、迁移和侵袭,蛋白质印迹检测SOCS5、细胞周期蛋白依赖性激酶-2(cyclin dependent protein kinase-2,CDK2)、神经型钙黏素(neural cadherin,N-cadherin)、上皮钙黏素(epithelical cadherin,E-cadherin)、波形蛋白(Vimentin)的表达,双荧光素酶报告基因实验检测miR-181a-3p与SOCS5 靶向关系.结果 与PBMCS细胞比较,MoIt4、Jurkat细胞miR-181a-3p表达水平增加(P<0.05),SOCS5 mRNA和蛋白表达水平降低(P<0.05);下调miR-181a-3p或过表达SOCS5 可降低MoIt4 细胞增殖活性、迁移细胞数、侵袭细胞数,下调N-cadherin、CDK2、Vimentin蛋白表达,上调E-cadherin蛋白表达(P<0.05);miR-181a-3p靶向负调控SOCS5,抑制SOCS5 逆转下调miR-181a-3p对MoIt4细胞增殖、侵袭、迁移和上皮间质转化(epithelial-to-mesenchymal transition,EMT)的影响.结论 miR-181a-3p靶向负调控SOCS5 抑制ALL细胞增殖、迁移、侵袭及EMT.
Objective To investigate the effect of microRNA(miRNA)-181 a-3 p on the ma-lignant progression of acute lymphoblastic leukemia(ALL)cells by targeting suppressor of cytokine signaling 5(SOCS5).Methods The expression levels of miR-181a-3p and SOCS5 in ALL cells were detected by RT-qPCR and Western blotting.MoIt4 cells were divided into 6 groups:anti-miR-NC group,anti-miR-181a-3p group,pcDNA group,PCDNA-SOCS5 group,anti-miR-181a-3p+si-NC group and anti-miR-181a-3p+si-SOCS5 group.RT-qPCR was used to detect the expression levels of miR-181a-3p and SOCS5.CCK8 and Transwell assay were used to detect cell proliferation,migration and invasion.Western blotting was used to detect the expression of SOCS5,CDK2,N-cadherin,E-cadherin and Vimentin.Dual luciferase gene reporter assay was used to detect the tar-geting relationship between miR-181a-3p and SOCS5.Results Compared with that in the PBMCS cells,the expression level of miR-181a-3p in the MoIt4 and Jurkat cells was increased(P<0.05),while the expression levels of SOCS5 mRNA and protein were decreased(P<0.05).Inhibition of miR-181a-3p or overexpression of SOCS5 decreased the proliferative activity,migra-tion and invasion of MoIt4 cells,and the expression levels of N-cadherin,CDK2 and Vimentin,and increased the expression level of E-cadherin(P<0.05).miR-181a-3p negatively targeted SOCS5,inhibition of SOCS5 reversed the effect of miR-181a-3p on the proliferation,migration,invasion and ep-ithelial-to-mesenchymal transition(EMT)in MoIt4 cells.Conclusion miR-181a-3p targets SOCS5 and negatively regulates the proliferation,migration,invasion and EMT of ALL cells.
陈静;吴胜;王珏;刘桦;夏楠;钱金锋;沙钰
扬州大学附属靖江人民医院病理科 江苏省靖江市,214500扬州大学附属靖江人民医院病理科 江苏省靖江市,214500扬州大学附属靖江人民医院病理科 江苏省靖江市,214500扬州大学附属靖江人民医院病理科 江苏省靖江市,214500扬州大学附属靖江人民医院病理科 江苏省靖江市,214500南通市第一人民医院病理科 江苏省 南通市,226001扬州大学附属靖江人民医院病理科 江苏省靖江市,214500
医药卫生
miR-181a-3p细胞因子信号传导抑制因子5急性淋巴细胞白血病增殖迁移侵袭上皮间质转化
miR-181a-3pSOCS5Acute lymphoblastic leukemiaProliferationMigra-tionInvadeEpithelial-to-mesenchymal transition
《医学分子生物学杂志》 2026 (2)
179-185,7
江苏省南通市卫生和计划生育委员会科研计划项目(No.WKZL2018019) This work was supported by a grant from the Research Project of Nantong Municipal Health and Family Planning Commission in Jiangsu Province(No.WKZL2018019)
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