首页|LINC00092靶向微小RNA-373-5p对骨肉瘤细胞迁移和侵袭的影响

LINC00092靶向微小RNA-373-5p对骨肉瘤细胞迁移和侵袭的影响

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目的 探究长基因间非蛋白编码RNA 92(LINC00092)在骨肉瘤细胞迁移和侵袭进展中的作用及潜在分子机制.方法 采用实时荧光定量PCR(qPCR)技术检测人成骨细胞(hFOB1.19)和骨肉瘤细胞系(SOSP-9607、U2-OS、Saos-2 和MG-63)中LINC00092 的表达水平.选取MG-63 细胞并分成LINC00092 组(LINC00092 过表达)、pcDNA组(阴性对照)和Con-trol组(空白对照).采用MTT、Transwell实验和划痕实验体外评估MG-63 细胞的增殖、侵袭和迁移能力.通过双荧光素酶报告基因实验、qPCR 和 Western blot 筛选并证实微小 RNA-373-5p(miR-373-5p)与 LINC00092 的靶向作用关系.结果 与hFOB1.19 细胞相比,LINC00092 在不同骨肉瘤细胞系中的表达均显著异常下调(P<0.05).与pcDNA组相比,LINC00092 组MG-63 细胞活力、细胞划痕愈合率和细胞穿膜数量均下降.miR-373-5p是LINC00092 的直接靶点且受其负调控(P<0.05).此外,LINC00092 组增殖细胞核抗原(PCNA)和基质金属蛋白酶 9(MMP9)的 mRNA 和蛋白水平下调(P<0.05).结论 LINC00092 可以靶向负调控miR-373-5p,并影响PCNA和MMP9 表达,抑制骨肉瘤细胞的增殖、迁移和侵袭过程.
Effects of LINC00092 on migration and invasion of osteosarcoma cells by targeting microRNA-373-5p
Objective To investigate the effects of long intergenic non-protein coding RNA 92(LINC00092)on migration and invasion progression of osteosarcoma cells as well as the underlying mechanism.Methods Quantitative real-time PCR(qPCR)was performed to detect the expression of LINC00092 in human normal osteoblasts hFOB1.19 cell line and osteosarcoma cell lines(SOSP-9607,U2-OS,Saos-2 and MG-63).MG-63 cells were cultured and divided into LINC00092 group(overexpression of LINC00092),pcDNA group(negative control)and Control group(blank control).MTT,Transwell assay and scratch assay were performed to determine proliferation,invasion and migration abilities of MG-63 cells.Moreover,the targeting relationship between microRNA-373-5p(miR-373-5p)and LINC00092 was verified by dual-luciferase reporter assay,qPCR and Western blot.Results Compared with hFOB1.19 cells,LINC00092 was significantly under-regulated in osteosarcoma cells(P<0.05).The cell vitality,healing rate of cell scratches and the number of cell penetrating membranes in LINC00092 group significantly decreased compared with pcDNA group.MiR-373-5p was able to act as a downstream target of LINC00092,and negatively regulated by LINC00092(P<0.05).Additionally,the expression of proliferating cell nuclear antigen(PCNA)and matrix metallopeptidase 9(MMP9)were inhibited in LINC00092 group on both mRNA and protein levels(P<0.05).Conclusion LINC00092 targets miR-373-5p,regulates PCNA and MMP9 expression,and suppresses the osteosarcoma cells'proliferation,migration and invasion.

OsteosarcomaLong intergenic non-protein coding RNA 92MicroRNA-373-5pInvasionMigration

周灏、许泽川、徐驰、王翔、况松、黄宇

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610100 成都 成都市龙泉驿区中医医院(成都中医药大学附属医院龙泉医院)骨伤科

610051 成都医学院第二附属医院核工业四一六医院脊柱骨科

骨肉瘤 长基因间非蛋白编码RNA 92 微小RNA-373-5p 侵袭 迁移

2023年成都市医学科研课题资助项目

2023294

2024

临床肿瘤学杂志
解放军第八一医院

临床肿瘤学杂志

CSTPCD
影响因子:1.583
ISSN:1009-0460
年,卷(期):2024.29(4)