临床外科杂志 ›› 2025, Vol. 33 ›› Issue (10): 1058-1063.doi: 10.3969/j.issn.1005-6483.20240498

• 论著 • 上一篇    下一篇

LINC00894调节微小RNA-495-3p/Rab23轴对肝癌细胞恶性生物学行为的影响

刘建 赫长胜 徐林海 陈鹏   

  1. 266300 山东青岛,青岛市胶州中心医院肝胆外科(刘建、赫长胜、徐林海);滕州市中心人民医院消化内科(陈鹏)
  • 收稿日期:2024-04-07 出版日期:2025-11-11 发布日期:2025-11-11
  • 通讯作者: 刘建,Email:l30eki@163.com
  • 基金资助:
    济宁医学院教师科研项目(JYFC2019FKJ301)

Effect of LINC00894 on the malignant biological behavior of liver cancer cells by regulating the microRNA-495-3p/Rab23 axis

LIU Jian*,HE Changsheng,XU Linhai,CHEN Pen   

  1. *Department of Hepatobiliary Surgery,Jiaozhou Central Hospital,Qingdao 266300,China
  • Received:2024-04-07 Online:2025-11-11 Published:2025-11-11

摘要: 目的 分析长链非编码RNA(lncRNA)LINC00894调节微小RNA(miR)-495-3p/RAS相关结合蛋白23(Rab23)轴对肝癌细胞恶性生物学行为的影响。方法 2023年1月~2023年11月行手术治疗的肝癌病人53例,取癌组织和癌旁组织,采用实时荧光定量聚合酶链反应(qRT-PCR)检测各组织及体外培养细胞Huh7、SMMC-7721、HepG2、L-02中LINC00894、miR-495-3p、Rab23表达。分析细胞Huh7,随机分为Huh7组、NC组、si-LINC00894组、anti-NC组、anti-miR-495-3p组。分别采用CCK-8、流式细胞术、Transwell法检测各组细胞增殖、凋亡、迁移及侵袭情况并进行比较,采用Western blot法测定细胞中Rab23、增殖相关蛋白表达。采用双荧光素酶报告基因实验分析并验证LINC00894和miR-495-3p、miR-495-3p和Rab23的关系。结果 肝癌组织及细胞中LINC00894、Rab23的mRNA相对表达量及蛋白表达较高,miR-495-3p的mRNA相对表达量较低,差异有统计学意义(P<0.05)。si-LINC00894组细胞凋亡率高于Huh7组和NC组,24小时、48小时、72小时吸光度、迁移、侵袭细胞数和细胞中Rab23表达低于Huh7组和NC组,差异有统计学意义(P<0.05);anti-miR-495-3p组24小时、48小时、72小时吸光度、迁移细胞数、侵袭细胞数和细胞中Rab23表达高于anti-NC组和si-LINC00894组,细胞凋亡率低于anti-NC组和si-LINC00894组,差异有统计学意义(P<0.05)。WT-LINC00894+miR-495-3p组荧光素酶活性低于WT-LINC00894+miR-NC组(P<0.05),WT-Rab23+miR-495-3p组荧光素酶活性低于WT-Rab23+miR-NC组,差异有统计学意义(P<0.05)。结论 LINC00894下调能促进miR-495-3p表达,抑制Rab23表达,进而对肝癌细胞恶性生物学行为具有抑制作用。

关键词: LINC00894, 微小RNA-495-3p/RAS相关结合蛋白23轴, 肝癌细胞, 恶性生物学行为

Abstract: Objective To analyze the effect of LINC00894 on the malignant biological behavior of liver cancer cells by regulating the microRNA(miR)-495-3p/RAS associated binding protein 23(Rab23) axis.Methods Cancer and adjacent tissues of 53 patients with liver cancer who undergoing surgery from January 2023 to November 2023 were collected.Real-time fluorescence quantitative polymerase chain reaction(qRT-PCR) was used to detect the expression of LINC00894,miR-495-3p and Rab23 in tissues and in vitro cultured cells Huh7,SMMC-7721,HepG2 and L-02.Cells Huh7 were randomly separated into Huh7 group,NC group,si-LINC00894 group,anti-NC group,and anti-miR-495-3p group.CCK-8,flow cytometry and Transwell were used to compare the cell proliferation, apoptosis,migration and invasion of each group.Western blot was used to detect the expression of Rab23 and proliferation-related proteins in cells.The relationship between LINC00894 and miR-495-3p,miR-495-3p and Rab23 was analyzed and verified by dual luciferase reporter gene assay.Results The mRNA and protein expression of LINC00894 and Rab23 were higher in cancer tissues and cells of liver cancer patients,while the mRNA expression of miR-495-3p was lower(P<0.05).The apoptosis rate of si-LINC00894 group was higher than that of Huh7 group and NC group,and the absorbance at 24 h,48 h,and 72 h,numbers of migrating and invading cells,and expression of Rab23 in cells were lower than those in Huh7 group and NC group(P<0.05);the absorbance at 24 h,48 h,and 72 h,numbers of migrating and invading cells,and expression of Rab23 in cells in the anti-miR-495-3p group were higher than those in the anti-NC group and si-LINC00894 group,the apoptosis rate of cells was lower than that in the anti NC group and si-LINC00894 group(P<0.05).The luciferase activity in the WT-LINC00894+miR-495-3p group was lower than that in the WT-LINC00894+miR-NC group(P<0.05),the luciferase activity in the WT-Rab23+miR-495-3p group was lower than that in the WT-Rab23+miR-NC group(P<0.05).Conclusion Downregulation of LINC00894 can promote the expression of miR-495-3p,inhibit the expression of Rab23,and thus exert the inhibitory effect on the malignant biological behavior of liver cancer cells.

Key words: LINC00894, microRNA-495-3p/RAS-associated binding protein 23 axis, liver cancer cells, malignant biological behavior

[1] 王振云, 王洪涛, 周瑞欣, 张津广. 艾司氯胺酮调节Wnt/β-catenin信号通路对肝癌细胞增殖、迁移和侵袭的影响[J]. 临床外科杂志, 2025, 33(4): 433-437.
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