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张波, 任龙飞, 胡进静, 白仲添, 周文策. 下调LncRNA LINC00857对胰腺癌PANC-1细胞增殖、迁移及凋亡的影响[J]. 肿瘤防治研究, 2021, 48(2): 127-132. DOI: 10.3971/j.issn.1000-8578.2021.20.0882
引用本文: 张波, 任龙飞, 胡进静, 白仲添, 周文策. 下调LncRNA LINC00857对胰腺癌PANC-1细胞增殖、迁移及凋亡的影响[J]. 肿瘤防治研究, 2021, 48(2): 127-132. DOI: 10.3971/j.issn.1000-8578.2021.20.0882
ZHANG Bo, REN Longfei, HU Jinjing, BAI Zhongtian, ZHOU Wence. Effect of LncRNA LINC00857 Knockdown on Migration, Proliferation and Apoptosis of Pancreatic Cancer PANC-1 Cells[J]. Cancer Research on Prevention and Treatment, 2021, 48(2): 127-132. DOI: 10.3971/j.issn.1000-8578.2021.20.0882
Citation: ZHANG Bo, REN Longfei, HU Jinjing, BAI Zhongtian, ZHOU Wence. Effect of LncRNA LINC00857 Knockdown on Migration, Proliferation and Apoptosis of Pancreatic Cancer PANC-1 Cells[J]. Cancer Research on Prevention and Treatment, 2021, 48(2): 127-132. DOI: 10.3971/j.issn.1000-8578.2021.20.0882

下调LncRNA LINC00857对胰腺癌PANC-1细胞增殖、迁移及凋亡的影响

Effect of LncRNA LINC00857 Knockdown on Migration, Proliferation and Apoptosis of Pancreatic Cancer PANC-1 Cells

  • 摘要:
    目的 探讨LncRNA LINC00857在胰腺细胞系中的表达及其下调对胰腺癌PANC-1细胞增殖、迁移和凋亡的影响,并探讨其机制。
    方法 构建慢病毒载体GV112,转染胰腺癌细胞株PANC-1为实验组,转染空白质粒为阴性对照组,未干预的细胞作为正常对照组;CCK-8法、Transwell实验、划痕实验、流式细胞术、Western blot检测下调LINC00857对细胞增殖、迁移、凋亡、细胞周期以及上皮间质转化(EMT)相关蛋白的影响。
    结果 胰腺癌细胞系中LINC00857的表达显著高于胰腺正常上皮细胞(P < 0.01)。敲低LINC00857可显著抑制PANC-1细胞的增殖和迁移能力(P < 0.0001);与阴性对照组相比,实验组细胞的凋亡率明显增加(P < 0.05),G0/G1期细胞数量增多(P < 0.01),S期细胞数目减少(P < 0.05),细胞被阻滞在G1期;E-cadherin表达显著上调(P < 0.05),N-cadherin和Vimentin表达显著下调(N-cadherin P < 0.01, Vimentin P < 0.05)。
    结论 LINC00857可通过调控G1/S期转化EMT信号通路促进PANC-1细胞的增殖和迁移,并抑制其凋亡。

     

    Abstract:
    Objective To investigate the expression of LncRNA LINC00857 in pancreatic cells and the effect of lncRNA LINC00857 down-regulation on proliferation, migration and apoptosis of pancreatic cancer PANC-1 cells and possible mechanism.
    Methods The lentiviral vector GV112 was constructed and infected PANC-1 cells to obtain experimental group, while the blank plasmid was transfected as a negative control group and the cells without intervention were taken as normal control group. CCK-8 assay, Transwell assay, scratch test, flow cytometry, Western blot were used to detect the effect of LINC00857 down-regulation on cell proliferation, migration, apoptosis, cell cycle and EMT-related proteins.
    Results LINC00857 expression in pancreatic cancer cells were significantly higher than that in normal pancreatic epithelial cells (P < 0.001). Knockdown of LINC00857 could significantly inhibit the proliferation and migration of PANC-1 cells (P < 0.0001); compared with the negative control group, the apoptosis rates of cells in the experimental groups were significantly increased (P < 0.05), the number of cells in G0/G1 phase increased (P < 0.01), the number of cells in S phase decreased (P < 0.05), and the cells were blocked in the G1 phase, E-cadherin expression was significantly up-regulated (P < 0.05) and N-cadherin and Vimentin expression were significantly down-regulated (N-cadherin: P < 0.01, Vimentin: P < 0.05).
    Conclusion LINC00857 can promote proliferation and migration of PANC-1 cells and inhibit its apoptosis by regulating G1/S phase transition and EMT signaling pathway.

     

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