医学分子生物学杂志 ›› 2024, Vol. 21 ›› Issue (3): 247-253.doi: 10.3870/j.issn.1672-8009.2024.03.009

• 论著 • 上一篇    下一篇

LINC00319 调控 PENK 调节 PI3K / AKT 信号通路在骨肉瘤中的机制研究 #br#

  

  1. 南通大学第二附属医院 (南通市第一人民医院) 手外科 江苏省南通市, 226000
  • 出版日期:2024-05-31 发布日期:2024-06-14
  • 基金资助:
    南通市卫健委课题 (No. MB2021023)

Mechanism of LINC00319 Regulating PENK / PI3K / AKT Signaling Pathway in Osteosarcoma #br#

  1. Department of Hand Surgery, Second Affiliated Hospital of Nantong University (Nantong First Peoples Hospital), Nantong, Jiangsu, 226000, China
  • Online:2024-05-31 Published:2024-06-14

摘要: 目的 探讨 LINC00319 调控前脑啡肽 ( proenkephalin, PENK) 调节 PI3K / AKT 信号通路在骨肉瘤 (osteosarcoma, OS) 中的机制方法 提取 OS 患者及非 OS 患者外周血 RNA, qPCR 法检测 LINC00319PENK 表达水平, 分析 LINC00319 PENK 相关性MG63 细胞中敲低或过表达 LINC00319, qPCR 及蛋白质印迹法分别检测 PENK mRNA 及蛋白表达。 OS 小鼠移植瘤模型分为 shNC 组及 shLINC00319 ,称量肿瘤重量, 免疫组化实验检测肿瘤组织中 PENK、 AKT、 p-AKT、 PI3K 的表达。 MG63 细胞分为 shNC、 shLINC00319 、 shLINC00319 + shPENK , EdU 法检测细胞增殖, Transwell 法检测细胞侵袭, 蛋白质印迹法检测 AKT、 p-AKT、 PI3K 蛋白表达水平结果 相较非 OS 患者, LINC00319 OS 患者外周血高表达, PENK OS 患者外周血低表达, PENK LINC00319 表达呈负相关敲低 LINC00319 , PENK mRNA 及蛋白水平上调, 过表达 LINC00319 , PENK mRNA 及蛋白水平下调相较于 shNC , shLINC00319组小鼠肿瘤重量降低, 肿瘤组织中 AKT 蛋白表达水平不变, p-AKT 蛋白表达水平降低, PI3K 蛋白表达水平降低相较于 shNC MG63 细胞, shLINC00319 组细胞增殖与侵袭能力降低, p-AKT、 PI3K 蛋白表达水平下降; 相较于 shLINC00319 组细胞, shLINC00319 + shPENK 组细胞的增殖与侵袭能力以及 p-AKT、 PI3K蛋白的表达水平均有所升高 结论LINC00319 OS 患者外周血高表达, PENK OS 患者外周血低表达,两者表达呈负相关性。 LINC00319 的高表达通过抑制 PENK 水平, 进而激活 PI3K / AKT 信号通路促进 OS 细胞增殖及细胞侵袭

关键词: 骨肉瘤, LINC00319, PENK, PI3K / Akt

Abstract: Objective To explore the mechanism of LINC00319 regulating PENK / PI3K / AKTsignal pathway in osteosarcoma (OS). Methods The expression levels of LINC00319 and PENK inthe peripheral blood RNAs from OS patients and non-OS patients were detected using qPCR, and the correlation between LINC00319 and PENK expression were analyzed. Knockdown or overexpression of LINC00319 were performed in the MG63 cells, and the mRNA and protein expression levels of PENK were detected using qPCR and Western blotting methods, respectively. The mouse OS transplanted tumor model was established and mice were divided into 2 groups: shNC group and shLINC00319 group. The tumor weight was measured, and the expression levels of PENK, AKT, p-AKT, and PI3K in the tumor tissues were detected through immunohistochemistry experiments. MG63 cells were divided into 3 groups: shNC group, shLINC00319 group, shLINC00319 + shPENK group. Cell proliferation was detected by EdU. Cell invasion was detected via transwell method. The protein expression levels of AKT, p-AKT, and PI3K were detected using Westernblotting. Results The expression level of LINC00319 was higher in the peripheral blood of OS patients, and the expression level of PENK was lower when compared to those in the peripheral blood of non-OS patients. The expression level of PENK was negatively correlated with the expression level of LINC00319. After knocking down LINC00319, PENK mRNA and protein levels were upregulated, while overexpression of LINC00319 resulted in decreased expression level of PENK mRNA and protein. Compared to mice in the shNC group, mice in the shLINC00319 group showed decreased tumor weight, unchanged expression level of AKT protein in tumor tissues, and deceased expression levels of p-AKT, PI3K protein. Compared to cells in the shNC group, MG63 cells in the shLINC00319 group showed decrease abilities in cell proliferation and invasion, the expression levels of p-AKT and PI3K proteins were decreased in the shLINC00319 group as well. Cells in the shLINC00319 + shPENK group showed increase abilities in cell proliferation and invasion, and the expression levels of p-AKT and PI3K proteins were increased when compared to those in theshLINC00319 group. Conclusion LINC00319 is highly expressed in the peripheral blood of OS patients, while PENK is lowly expressed in the peripheral blood of OS patients, and their expression levels are negatively correlated. LINC00319 promotes OS cell proliferation and invasion by inhibiting PENK levels and activating the PI3K / AKT signaling pathway.

Key words: osteosarcoma, LINC00319, proenkephalin, PI3K / Akt

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