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盛晶, 万里新, 屈中玉. miR-23a靶向NID2通过Notch通路调控肺癌细胞的侵袭和迁移[J]. 肿瘤防治研究, 2017, 44(6): 381-386. DOI: 10.3971/j.issn.1000-8578.2017.17.0035
引用本文: 盛晶, 万里新, 屈中玉. miR-23a靶向NID2通过Notch通路调控肺癌细胞的侵袭和迁移[J]. 肿瘤防治研究, 2017, 44(6): 381-386. DOI: 10.3971/j.issn.1000-8578.2017.17.0035
SHENG Jing, WAN Lixin, QU Zhongyu. miR-23a Targeting NID2 Regulates Invasion and Migration of Lung Cancer Cells Through Notch Pathway[J]. Cancer Research on Prevention and Treatment, 2017, 44(6): 381-386. DOI: 10.3971/j.issn.1000-8578.2017.17.0035
Citation: SHENG Jing, WAN Lixin, QU Zhongyu. miR-23a Targeting NID2 Regulates Invasion and Migration of Lung Cancer Cells Through Notch Pathway[J]. Cancer Research on Prevention and Treatment, 2017, 44(6): 381-386. DOI: 10.3971/j.issn.1000-8578.2017.17.0035

miR-23a靶向NID2通过Notch通路调控肺癌细胞的侵袭和迁移

miR-23a Targeting NID2 Regulates Invasion and Migration of Lung Cancer Cells Through Notch Pathway

  • 摘要:
    目的 探讨miR-23a靶向调控NID2蛋白的表达通过Notch通路对肺癌细胞的生物学行为的影响及其机制。
    方法 免疫组织化学检测NID2在肺癌和癌旁正常肺组织中的表达;Western blot检测不同肺癌细胞株中NID2的表达;荧光素酶报告基因检测miR-23a与NID2的相互作用;Transwell侵袭和划痕实验检测miR-23a的表达对肺癌细胞侵袭和迁移能力的影响;Western blot检测过表达miR-23a后肺癌H1650细胞中hes1和NICD蛋白的表达。
    结果 与癌旁正常肺组织相比,肺癌组织中NID2表达明显增高;H1650肺癌细胞株中NID2的表达水平最高;在肺癌H1650细胞中,miR-23a能与NID2的3’UTR特异性结合,调控NID2的表达;miR-23a可调控肺癌H1650细胞的侵袭迁移能力;过表达miR-23a可以抑制肺癌H1650细胞中hes1和NICD的表达。
    结论 miR-23a可以靶向NID2通过Notch信号通路调控肺癌细胞的侵袭和迁移。

     

    Abstract:
    Objective To investigate the effect of miR-23a targeting NID2 on the biological behavior of lung cancer cells through Notch pathway and related mechanism.
    Methods Immunohistochemistry was used to detect the expression of NID2 in lung cancer tissues and adjacent normal lung tissues. The expressions of NID2 in different lung cancer cell lines were detected by Western blot. Luciferase reporter gene was used to detect the interaction between miR-23a and NID2. Transwell invasion assay and scratch assay were used to detect the effect of miR-23a expression on the invasion and migration abilities of lung cancer cells. The expression of hes1 and NICD were detected in H1650 lung cancer cell line by Western blot.
    Results The expression of NID2 in lung cancer tissues was significantly higher than that in adjacent normal lung tissues. The expression level of NID2 in H1650 lung cancer cell line was the highest; miR-23a can regulate the expression of NID2. miR-23a can regulate the invasion and migration of lung cancer H1650 cells. The expression of hes1 and NICD were deceased in H1650 lung cancer cell line by the overexpression of miR-23a.
    Conclusion miR-23a targeting NID2 can regulate the invasion and migration of lung cancer cells through Notch signaling pathway.

     

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