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胡会杰, 郑晓璐, 雷立峰. 柠檬苦素通过调节JAK2/STAT3信号通路对非小细胞肺癌细胞恶性生物学行为的影响[J]. 肿瘤防治研究, 2023, 50(12): 1191-1196. DOI: 10.3971/j.issn.1000-8578.2023.23.0399
引用本文: 胡会杰, 郑晓璐, 雷立峰. 柠檬苦素通过调节JAK2/STAT3信号通路对非小细胞肺癌细胞恶性生物学行为的影响[J]. 肿瘤防治研究, 2023, 50(12): 1191-1196. DOI: 10.3971/j.issn.1000-8578.2023.23.0399
HU Huijie, ZHENG Xiaolu, LEI Lifeng. Influence of Limonin on Malignant Biological Behavior of Non-small Cell Lung Cancer Cells by Regulating JAK2/STAT3 Signaling Pathway[J]. Cancer Research on Prevention and Treatment, 2023, 50(12): 1191-1196. DOI: 10.3971/j.issn.1000-8578.2023.23.0399
Citation: HU Huijie, ZHENG Xiaolu, LEI Lifeng. Influence of Limonin on Malignant Biological Behavior of Non-small Cell Lung Cancer Cells by Regulating JAK2/STAT3 Signaling Pathway[J]. Cancer Research on Prevention and Treatment, 2023, 50(12): 1191-1196. DOI: 10.3971/j.issn.1000-8578.2023.23.0399

柠檬苦素通过调节JAK2/STAT3信号通路对非小细胞肺癌细胞恶性生物学行为的影响

Influence of Limonin on Malignant Biological Behavior of Non-small Cell Lung Cancer Cells by Regulating JAK2/STAT3 Signaling Pathway

  • 摘要:
    目的 探讨柠檬苦素调节JAK2/STAT3信号通路对非小细胞肺癌(NSCLC)细胞恶性生物学行为的影响。
    方法 CCK-8法检测不同浓度的柠檬苦素(0、5、10、25、50、75、100 μmol/L)干预对A549细胞存活率的影响;将A549细胞分为NC组(正常培养)、柠檬苦素低剂量组(10 μmol/L柠檬苦素干预细胞24 h)、柠檬苦素中剂量组(25 μmol/L柠檬苦素干预细胞24 h)、柠檬苦素高剂量组(50 μmol/L柠檬苦素干预细胞24 h)、Coumermycin A1组(10 μmol/L JAK2激活剂Coumermycin A1+50 μmol/L柠檬苦素干预细胞24 h)、AG490组(10 μmol/L JAK2抑制剂AG490+50 μmol/L柠檬苦素干预细胞24 h);克隆形成实验检测各组细胞克隆情况;Transwell小室检测各组细胞迁移和侵袭;流式细胞术检测各组细胞凋亡情况;Western blot检测各组细胞JAK2、p-JAK2、STAT3、p-STAT3、E-Cadherin、N-Cadherin和Vimentin蛋白表达情况。
    结果 与0 μmol/L柠檬苦素组相比,A549细胞存活率呈柠檬苦素浓度依赖性降低(P < 0.05),IC50为(45.16±1.66)μmol/L,选择10、25和50 μmol/L进行后续实验;与NC组相比,柠檬苦素低、中、高剂量组A549细胞克隆数、迁移和侵袭数以及IL-6、p-JAK2、p-STAT3、N-Cadherin和Vimentin蛋白表达降低,细胞凋亡率和E-Cadherin蛋白表达升高(P < 0.05);JAK2激活剂Coumermycin A1减弱了柠檬苦素对A549细胞增殖、迁移、侵袭等恶性生物学行为的抑制能力,减弱细胞凋亡能力;JAK2抑制剂AG490增强了柠檬苦素对A549细胞增殖、迁移、侵袭等恶性生物学行为的抑制能力,增强了细胞凋亡能力。
    结论 柠檬苦素可通过抑制JAK2/STAT3通路进而抑制NSCLC细胞增殖、迁移、侵袭等恶性生物学行为。

     

    Abstract:
    Objective To investigate the influence of limonin on the malignant biological behavior of non-small cell lung cancer (NSCLC) cells by regulating the protein tyrosine kinase 2 (JAK2)/signal transducer and activator of transcription 3 (STAT3) signaling pathway.
    Methods CCK-8 method was applied to detect the survival rate of A549 cells treated with different concentrations of limonin (0, 5, 10, 25, 50, 75, 100 μmol/L). A549 cells were separated into normal culture (NC) group, low-dose limonin group (treatment with 10 μmol/L limonin for 24 h), medium-dose limonin group (treatment with 25 μmol/L limonin for 24 h), high-dose limonin group (treatment with 50 μmol/L limonin for 24 h), coumermycin A1 group (treatment with 10 μmol/L JAK2 activator coumermycin A1+50 μmol/L limonin for 24 h), and AG490 group (treatment with 10 μmol/L JAK2 inhibitor AG490+50 μmol/L limonin for 24 h). Clone formation assay was applied to detect the clones of each group of cells. Transwell assay was applied to detect cell migration and invasion, and flow cytometry was applied to detect apoptosis. Western blot analysis was applied to detect the protein expression levels of JAK2, p-JAK2, STAT3, p-STAT3, E-cadherin, N-cadherin, and vimentin in each group.
    Results The viability of A549 cells decreased significantly in a limonin concentration-dependent manner (P < 0.05), with IC50 of 45.16±1.66 μmol/L. Concentrations of 10, 25, and 50 μmol/L were selected for subsequent experiments. The numbers of clones, migration, and invasion of A549 cells and the protein expression levels of IL-6, p-JAK2, p-STAT3, N-cadherin, and vimentin in the low-, medium-, and high-dose limonin groups significantly decreased, compared with those in the NC group, and the apoptosis rate and E-cadherin protein expression significantly increased (P < 0.05). The JAK2 activator coumermycin A1 attenuated the ability of limonin to inhibit the proliferation, migration, invasion, and other malignant biological behavior of A549 cells and attenuated the apoptosis ability. The JAK2 inhibitor AG490 enhanced the ability of limonin to inhibit the proliferation, migration, invasion, and other malignant biological behavior of A549 cells and enhanced the apoptosis ability.
    Conclusion Limonin can inhibit the malignant biological behavior of NSCLC cells, such as proliferation, migration, and invasion, by inhibiting the JAK2/STAT3 pathway.

     

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