首页|LINC00852调节miR-671-5p/MYH9信号轴对非小细胞肺癌细胞增殖侵袭及迁移的影响

LINC00852调节miR-671-5p/MYH9信号轴对非小细胞肺癌细胞增殖侵袭及迁移的影响

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目的:探讨长链非编码RNA00852(LINC00852)调节微小 RNA-671-5p(miR-671-5p)/肌球蛋白重链9(MYH9)信号轴对非小细胞肺癌(NSCLC)细胞增殖、侵袭及迁移的影响。方法:采用qRT-PCR法检测 45 例 2022 年 9 月至 2023 年 12 月期间在我院进行手术的 NSCLC 患者术中切除的NSCLC组织及癌旁组织中 LINC00852、miR-671-5p、MYH9 mRNA 的表达。以 A549 细胞为研究对象,将其随机分为Control组、sh-NC组、sh-LINC00852 组、sh-LINC00852+anti-NC 组、sh-LINC00852+anti-miR-671-5p组。检测各组中LINC00852、miR-671-5p、MYH9 mRNA 的表达;平板克隆实验、Transwell实验、划痕实验分别检测敲低LINC00852 对A549 细胞的增殖、侵袭、迁移的影响;Western blot检测各组A549 细胞中PCNA、MYH9、MMP-9 蛋白的表达。双荧光素酶报告基因实验检测 LINC00852 与 miR-671-5p、miR-671-5p与MYH9 之间的互作。结果:NSCLC组织LINC00852(1。65±0。34)、MYH9 mRNA表达(1。73±0。35)高于癌旁组织[(0。98±0。29)、(1。01±0。33)](t=10。058、10。041,P<0。05),miR-671-5p表达(0。52±0。15)低于癌旁组织(1。00±0。18)(t=13。742,P<0。05)。sh-LINC00852 组 A549 细胞的克隆数、侵袭数、划痕愈合率、LINC00852、MYH9 mRNA和蛋白、PCNA蛋白、MMP-9 蛋白表达低于sh-NC组、Control组,miR-671-5p 表达高于 sh-NC 组、Control 组(P<0。05);与 sh-LINC00852 组、sh-LINC00852+anti-NC 组相比,sh-LINC00852+anti-miR-671-5p 组克隆数、侵袭数、划痕愈合率、MYH9 mRNA和蛋白、PCNA蛋白、MMP-9 蛋白表达升高,miR-671-5p 表达降低(P<0。05)。LINC00852 可以靶向负调控 miR-671-5p,miR-671-5p 可以靶向负调控 MYH9。结论:敲低 LINC00852 可以抑制NSCLC细胞的增殖、侵袭、迁移,其机制可能是通过调控miR-671-5p/MYH9 信号通路实现的。
Effect of LINC00852 Regulating the miR-671-5p/MYH9 Signaling Axis on Proliferation Invasion and Migration of Non-Small Cell Lung Cancer Cells
Objective:To investigate the effects of long non-coding RNA 00852(LINC00852)on the proliferation,invasion,and migration of non-small cell lung cancer(NSCLC)cells by regulating the microR-NA-671-5p(miR-671-5p)/myosin heavy chain 9(MYH9)signaling axis.Methods:The expression levels of LINC00852,miR-671-5p,and MYH9 mRNA were detected in NSCLC tissues and adjacent normal tissues using qRT-PCR.A549 cells were randomly divided into several groups:Control group,sh-NC group,sh-LINC00852 group,sh-LINC00852+anti-NC group,and sh-LINC00852+anti-miR-671-5p group.The ex-pression levels of LINC00852,miR-671-5p,and MYH9 mRNA were detected.Cell proliferation,invasion,and migration were assessed by colony formation assay,Transwell assay,and wound healing assay,respective-ly.Western blot was used to detect the protein expression of PCNA,MYH9,and MMP-9.Dual-luciferase reporter assay was performed to verify the interaction between LINC00852 and miR-671-5p,and between miR-671-5p and MYH9.Results:The expression levels of LINC00852 and MYH9 mRNA were significantly higher in NSCLC tissues compared with adjacent normal tissues,while the expression of miR-671-5p was sig-nificantly lower.Knockdown of LINC00852 inhibited the proliferation,invasion,and migration of A549 cells,and downregulated the expression of MYH9,PCNA,and MMP-9,while upregulating the expression of miR-671-5p.Dual-luciferase reporter assay confirmed that LINC00852 could directly target miR-671-5p,and miR-671-5p could directly target MYH9.Conclusion:LINC00852 inhibits the proliferation,invasion,and migration of NSCLC cells by regulating the miR-671-5p/MYH9 signaling axis.

Long non-coding RNA 00852microRNA-671-5pMyosin heavy chain 9Non-small cell lung cancerProliferationInvasionMigration

李亚明、张进召、刘松、潘双、刘佳银

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西安医学院第一附属医院呼吸与危重症医学科,陕西 西安 710077

长链非编码RNA00852 微小RNA-671-5p 肌球蛋白重链9 非小细胞肺癌 增殖 侵袭 迁移

陕西省重点研发计划项目

2022SF-554

2024

河北医学
河北省医学会

河北医学

CSTPCD
影响因子:1.915
ISSN:1006-6233
年,卷(期):2024.30(10)