首页|长链非编码RNA GAS5靶向微小RNA-106b-5p对胃癌细胞增殖、迁移和侵袭的影响

长链非编码RNA GAS5靶向微小RNA-106b-5p对胃癌细胞增殖、迁移和侵袭的影响

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目的 观察长链非编码RNA(lncRNA)GAS5靶向微小RNA(miR)-106b-5p对胃癌细胞增殖、迁移和侵袭的影响.方法 收集112例胃癌组织和癌旁组织作为研究对象,采用荧光定量聚合酶链反应(PCR)分析组织中lncRNA GAS5和miR-106b-5p的表达水平.HGC-27细胞随机分为lncRNA对照组、lncRNA GAS5组、miRNA对照组和miR-106b-5p KD组,分别采用慢病毒建立lncRNA GAS5过表达和miR-106b-5p敲减细胞系.细胞计数试剂盒(CCK-8)、划痕实验、Transwell实验检测各组的细胞增殖、迁移及侵袭能力;双荧光素酶报告基因分析lncRNA GAS5和miR-106b-5p关系.组间比较采用t检验.结果 癌旁组织中lncRNA GAS5表达量(1.003±0.107)显著高于胃癌组织(0.387±0.060),差异有统计学意义(t=8.649,P<0.05).lncRNA GAS5 组细胞 lncRNA GAS5表达水平(3.073±0.373)明显高于lncRNA对照组(1.007±0.097),差异有统计学意义(t=9.284,P<0.05).miR-106b-5p 敲减组细胞 miR-106b-5p 表达水平(0.333±0.283)明显低于miRNA对照组(1.123±0.076),差异有统计学意义(t=11.880,P<0.05).lncRNA GAS5组吸光度值(1.453±0.090)明显低于lncRNA对照组(1.983±0.196),差异有统计学意义(t=4.254,P<0.05).miR-106b-5p 敲减组吸光度值(1.277±0.081)明显低于 miRNA 对照组(2.083±0.191),差异有统计学意义(t=6.781,P<0.05).lncRNA GAS5组细胞划痕愈合率[(43.347±4.713)%]明显低于lncRNA对照组[(79.643±7.069)%],差异有统计学意义(t=7.399,P<0.05).miR-106b-5p敲减组细胞划痕愈合率[(39.773±1.817)%]明显低于miRNA对照组[(82.547± 2.811)%],差异有统计学意义(t=18.633,P<0.05).lncRNA GAS5 组细胞侵袭数量[(58.137± 5.167)个]明显低于lncRNA对照组[(89.733±8.942)个],差异有统计学意义(t=5.128,P<0.05).miR-106b-5p敲减组细胞侵袭数量[(51.917±2.671)个]显著低于miRNA对照组[(92.473± 6.209)个],差异有统计学意义(t=10.393,P<0.05).lncRNA GAS5与miR-106b-5p呈碱基互补.lncRNA GAS5 组细胞 miR-106b-5p 表达水平(0.563±0.067)明显低于 lncRNA 对照组(1.187± 0.100),差异有统计学意义(t=8.976,P<0.05).结论 lncRNA GAS5在胃癌中表达上调,而miR-106b-5p表达水平下调,lncRNA GAS5通过竞争吸附结合miR-106b-5p调节胃癌细胞增殖、迁移和侵袭.
Effects of long non-coding RNA GAS5 targeting microRNA-106b-5p on proliferation,migration and invasion of gastric cancer cells
Objective To observe the effects of long non-coding RNA(lncRNA)GAS5 targeting microRNA(miR)-106b-5p on proliferation,migration and invasion of gastric cancer cells.Methods A total of 112 gastric cancer tissues and adjacent tissues were selected as the research objects.The expression levels of lncRNA GAS5 and miR-106b-5p in tissues were detected by fluorescence quantitative polymerase chain re-action(PCR).HGC-27 cells were randomly divided into lncRNA control group,lncRNA GAS5 group,miRNA control group and miR-106b-5p KD group.LncRNA GAS5 overexpression and miR-106b-5p knock-down cell lines were established by lentivirus,respectively.Cell counting kit-8(CCK-8),scratch and Tran-swell assays were used to analyze cell proliferation,migration and invasion in each group,respectively.The relationship between lncRNA GAS5 and miR-106b-5p was analyzed by bioinformatics and dual lucifer-ase reporter gene.T-test was used for inter group comparison.Results The expression level of lncRNA GAS5 in paracancer tissues(1.003±0.107)was significantly lower than that in gastric cancer tissues(0.387±0.060,t=8.649,P<0.05).The expression level of lncRNA GAS5 in lncRNA GAS5 group(3.073±0.373)was significantly higher than that in lncRNA control group(1.007±0.097,t=9.284,P<0.05).The expression level of miR-106b-5p in miR-106b-5p knockout group(0.333±0.283)was significantly lower than that in miRNA control group(1.123±0.076,t=11.880,P<0.05).The absor-bance value of lncRNA GAS5 group(1.453±0.090)was significantly lower than that of lncRNA control group(1.983±0.196,t=4.254,P<0.05).The absorbance of miR-106b-5p knockout group(1.277± 0.081)was significantly lower than that of miRNA control group(2.083±0.191,t=6.781,P<0.05).The scratch healing rate of lncRNA GAS5 group[(43.347±4.713)%]was significantly lower than that of lncRNA control group[(79.643±7.069)%,t=7.399,P<0.05).The scratch healing rate of miR-106b-5p knockout group[(39.773±1.817)%]was significantly lower than that of miRNA control group[(82.547±2.811)%,t=18.633,P<0.05].The number of invasive cells in lncRNA GAS5 group[(58.137±5.167)]was significantly less than that in lncRNA control group[(89.733±8.942),t=5.128,P<0.05].The number of invasive cells in miR-106b-5p knockout group[(51.917±2.671)]was significantly less than that in miRNA control group[(92.473±6.209),t=10.393,P<0.05].LncRNA GAS5 and miR-106b-5p had base complementary.The expression level of miR-106b-5p in ln-cRNA GAS5 group(0.563±0.067)was significantly lower than that in lncRNA control group(1.187± 0.100,t=8.976,P<0.05).Conclusion lncRNA GAS5 expression is up-regulated in gastric cancer tissues,and the expression of miR-106b-5p is down-regulated.LncRNA GAS5 regulates the proliferation,migration and invasion of gastric cancer cells through competitive adsorption and binding to miR-106b-5p.

Long non-coding RNAMicroRNAGastric cancerProliferationMigration

温一阳、徐成阳、胡晓舒

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河南省人民医院肿瘤中心/郑州大学人民医院/河南大学人民医院肿瘤科,郑州 450003

河南中医药大学第五临床医学院(郑州人民医院)病理科,郑州 450003

长链非编码RNA 微小RNA 胃癌 增殖 迁移

河南省医学科技攻关计划项目

LHGJ20220003

2024

中华实验外科杂志
中华医学会

中华实验外科杂志

CSTPCD
影响因子:0.759
ISSN:1001-9030
年,卷(期):2024.41(2)
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