首页> 外文期刊>European review for medical and pharmacological sciences. >LncRNA ADPGK-AS1 regulated cell proliferation, invasion, migration and apoptosis via targeting miR-542-3p in osteosarcoma
【24h】

LncRNA ADPGK-AS1 regulated cell proliferation, invasion, migration and apoptosis via targeting miR-542-3p in osteosarcoma

机译:LNCRNA ADPGK-AS1受骨肉瘤中靶向miR-542-3p的调节细胞增殖,侵袭,迁移和细胞凋亡

获取原文
           

摘要

OBJECTIVE: The functions of lncRNAs have been verified to be important biomarkers and regulators for diagnosis and treatment of human diseases. In osteosarcoma (OS), emerging evidence determined that lncRNA was associated with cell progression. However, due to the high incidence and recurrence rate of osteosarcoma, it is important to find an effective treatment for osteosarcoma. PATIENTS AND METHODS: QRT-PCR was used to detect the expression of ADPGK-AS1 and miR-542-3p in tissues and cells. Western blot was applied to measure the protein expression of CDK4, Cyclin D1, Bcl-2, Bax, Cleaved caspase-3, MMP-2, and MMP-9. MTT assay and flow cytometry were used to measure cell proliferation and apoptosis. Cell invasion and migration were determined using the transwell assay. Moreover, luciferase reporter assay was used to ensure the relation between ADPGK-AS1 and miR-542-3p. RESULTS: LncRNA ADPGK-AS1 expression was induced while miR-542-3p expression was reduced in OS tissues and cells. Functional experiments showed that inhibition of ADPGK-AS1 could decrease cell proliferation, migration, and invasion, as well as promoted cell apoptosis in OS cells. Also, miR-542-3p has been verified to be a target miRNA of ADPGK-AS1 and miR-542-3p could reverse the effects of ADPGK-AS1 on cell proliferation, apoptosis, migration, and invasion in OS cells. CONCLUSIONS: ADPGK-AS1 affected cell proliferation, invasion, migration, and apoptosis via targeting miR-542-3p in OS, providing a theoretical basis and a new therapeutic target for the diagnosis and treatment of OS.
机译:目的:LNCRNA的功能已被验证为诊断和治疗人类疾病的重要生物标志物和调节因素。在骨肉瘤(OS)中,出现的证据确定LNCRNA与细胞进展相关。然而,由于骨肉瘤的发病率高和复发率,重要的是找到对骨肉瘤的有效治疗方法。患者和方法:QRT-PCR用于检测组织和细胞中ADPGK-AS1和miR-542-3P的表达。施用蛋白质印迹以测量CDK4,Cyclin D1,Bcl-2,Bax,切割的Caspase-3,MMP-2和MMP-9的蛋白质表达。 MTT测定和流式细胞术用于测量细胞增殖和凋亡。使用Transwell测定法测定细胞侵袭和迁移。此外,使用荧光素酶报告器测定法确保ADPGK-AS1和MIR-542-3P之间的关系。结果:诱导LNCRNA ADPGK-AS1表达,而MIR-542-3P表达在OS组织和细胞中降低。功能实验表明,ADPGK-AS1的抑制可以降低细胞增殖,迁移和侵袭,以及促进OS细胞的细胞凋亡。此外,MIR-542-3P已被验证为ADPGK-AS1的靶miRNA,MiR-542-3P可以逆转ADPGK-AS1对OS细胞中细胞增殖,细胞凋亡,迁移和侵袭的影响。结论:ADPGK-AS1通过靶向MIR-542-3P在OS中受到影响的细胞增殖,侵袭,迁移和细胞凋亡,为OS的诊断和治疗提供了理论依据和新的治疗目标。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号