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miR-483-3p靶向CD44抑制EGFR突变肺癌的作用研究 被引量:3

Inhibitory Effect of miR-483-3p on the EGFR-mutant Lung Cancer Via Targeting CD44
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摘要 目的:探讨mi R-483-3p对CD44表达的调控作用及采用脂质体载药系统递送mi R-483-3p治疗表皮生长因子(epidermalgrowth factor receptor,EGFR)突变的非小细胞肺癌(non-small cell lung cancer,NSCLC)的作用。方法:通过mi R-483-3p靶基因的数据库发现CD44可能是mi R-483-3p的靶基因之一,从结构上及功能上进行验证。在EGFR酪氨酸激酶抑制剂(epidermal growth factor receptor-tyrosine kinase inhibitor, EGFR-TKI)耐药的NSCLC模型中,分别从基因及蛋白水平检测耐药模型及敏感模型中CD44的表达。在HCC827GR移植瘤模型中,采用脂质体-鱼精蛋白-DNA (liposome-polycation-DNA, LPD)载药系统递送mi R-483-3p进行治疗,观察肿瘤的生长情况。结果:双荧光素酶报告基因实验及Western blot实验结果显示CD44是mi R-483-3p的靶基因之一,且CD44在EGFR-TKI耐药模型中异常高表达(P<0.05)。脂质体载药系统LPD-mi RNA-DSPE-PEG符合静脉给药要求,Size为66.93±21 nm,Zeta potential为8.7±2 m V,PDI (Polydispersity Index)为0.1,递送mi R-483-3p后能够抑制HCC827GR移植瘤的生长(P<0.05)。结论:CD44为mi R-483-3p的靶基因之一,在耐药模型中高表达,脂质体载药系统给予mi R-483-3p能够抑制EGFR-TKI耐药肿瘤的生长。 Objective:To investigate the regulation of mi R-483-3 p on CD44 and the treatment of mi R-483-3 p in EGFR(epidermal growth factor receptor)mutations non-small cell lung cancer(NSCLC)by liposome drug delivery system.Methods:CD44 was found to be one of the target genes of mi R-483-3 p in the database,and was verified structurally and functionally.In the EGFR Tyrosine Kinase Inhibitor(EGFR-TKI)-resistant model of NSCLC,the expression of CD44 which was detected from gene and protein levels in the resistant and sensitive models.In the xenograft model of HCC827 GR,mi R-483-3 p was delivered for treatment by the liposomeprotamine-DNA(LPD)drug delivery system to observe the growth of tumor.Results:Dual-Luciferase Reporter Assay System and Western Blot showed that CD44 was one of the target genes of mi R-483-3 p,and CD44 was abnormally highly expressed in the EGFR-TKI resistant model in vitro and in vivo(P<0.05).The LPD-mi RNA-DSPE-PEG prepared by the liposome drug-loading system met the requirements of intravenous administration,Size:66.93±21 nm,Zeta potential:8.7±2 m V,Polydispersity Index:0.1,which could inhibit the growth of HCC827 GR-xenograft-model after delivery of mi R-483-3 p by LPD-mi RNA-DSPE-PEG(P<0.05).Conclusions:CD44 is one of the target genes of mi R-483-3 p and is highly expressed in the resistant model.The liposome drug delivery system about mi R-483-3 p can inhibit the growth of EGFR-TKI resistant tumors.
作者 王彩云 吕大成 李羚 王涛 胡梦笛 徐璐 WANG Cai-yun;LV Da-cheng;LI Ling;WANG Tao;HU Meng-di;XU Lu(Department of Pharmacology and Chemical Biology,Shanghai Jiao Tong University School of Medicine,Shanghai,200025,China)
出处 《现代生物医学进展》 CAS 2019年第14期2601-2608,共8页 Progress in Modern Biomedicine
基金 国家自然科学基金项目(81372522 81773747) 上海市科委基金项目(12ZR1416000 12140901400)
关键词 miR-483-3p 非小细胞肺癌 EGFR酪氨酸激酶抑制剂 CD44 脂质体 miR-483-3p NSCLC EGFR-TKI CD44 Liposome
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