| 引用本文: | 周巧巧,张彬,匡政坤,周诗毅,谭芬.一种新型多环螺环氧化吲哚类化合物对肺癌细胞系的生长抑制作用及其机制[J].中国现代应用药学,2023,40(12):1720-1727. |
| ZHOU Qiaoqiao,ZHANG Bin,KUANG Zhengkun,ZHOU Shiyi,TAN Fen.Inhibitory Effect and Mechanism of a Novel Polycyclic Spiro-epoxy Indole Compound on Lung Cell Lines Proliferation[J].Chin J Mod Appl Pharm(中国现代应用药学),2023,40(12):1720-1727. |
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| 一种新型多环螺环氧化吲哚类化合物对肺癌细胞系的生长抑制作用及其机制 |
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周巧巧1,2, 张彬1,2, 匡政坤1,2, 周诗毅1,2, 谭芬1,2
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1.湖北第二师范学院化学与生命科学学院, 武汉 430205;2.湖北第二师范学院化学与生命科学学院植物抗癌活性物质提纯与应用湖北省重点实验室, 武汉 430205
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| 摘要: |
| 目的 探究一种新型多环螺环氧化吲哚化合物对肺细胞系生长抑制的作用与机制。方法 首先通过MTT试验、流式细胞技术与细胞划痕试验检测化合物对肺癌细胞系的增殖、细胞凋亡以及细胞迁移的影响。接着通过PharmMapper平台预测其靶标蛋白，通过GEPIA平台预测与该靶蛋白具有较强相关性的蛋白，最后分别通过双荧光素酶报告基因试验，qPCR试验以及免疫印迹试验，在启动子水平、转录水平和表达水平检测化合物对目的基因的影响。结果 实验结果表明化合物能够显著抑制SKLU1细胞系的增殖，IC50值为11.38 μmol·L-1，化合物浓度>2.85 μmol·L-1即能够抑制SKLU1的细胞迁移，浓度>5.69 μmol·L-1能够诱导细胞凋亡。其分子机理可能是通过靶向RhoGEF7蛋白，下调下游的Rac1蛋白表达量，从而下调E-cadherin蛋白表达量，抑制细胞迁移；并且，下调的Rac1蛋白还能抑制NF-κB的激活，下调下游基因IL-6和IL-8的转录；下调的Rac1蛋白还能抑制IL-6/JAK/STAT3通路。结论 本研究为这种新型多环螺环氧化吲哚化合物靶向肺癌细胞的分子机制提供理论依据。 |
| 关键词: 多环螺环氧化吲哚 SKLU1 RhoGEF7 IL-6/JAK/STAT3 NF-κB激活 |
| DOI：10.13748/j.cnki.issn1007-7693.20221919 |
| 分类号:R965.2 |
| 基金项目:湖北省自然科学基金项目(2022CFB413)；湖北省教育厅科研计划项目(Q20233004) |
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| Inhibitory Effect and Mechanism of a Novel Polycyclic Spiro-epoxy Indole Compound on Lung Cell Lines Proliferation |
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ZHOU Qiaoqiao1,2, ZHANG Bin1,2, KUANG Zhengkun1,2, ZHOU Shiyi1,2, TAN Fen1,2
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1.School of Chemistry and Life Sciences, Hubei University of Education, Wuhan 430205, China;2.Hubei Key Laboratory of Purification and Application of Plant Anti-cancer Active Ingredients, School of Chemistry and Life Sciences, Hubei University of Education, Wuhan 430205, China
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| Abstract: |
| OBJECTIVE To explore the effect and mechanism of a novel polycyclic spiro-epoxy indole compound on suppression of lung cell lines proliferation. METHODS The compound’s effect on cellular proliferation, apoptosis, and cellular migration was determined using the MTT assays, flow cytometry, and cell scratch test. The target proteins of this compound were then predicted using the PharmMapper platform, while the associated proteins in lung adenocarcinoma were predicted using the GEPIA platform. In order to determine the effect of this compound on the target gene at the promoter level, transcription level, and expression level, reporter gene assay, qPCR assay and Western blotting test were also performed. RESULTS The results showed that this compound inhibited the proliferation of SKLU1 cell line with an IC50 value of 11.38 μmol·L-1, inhibited the cell migration of SKLU1 above the concentration of 2.85 μmol·L-1, and induced the apoptosis above the concentration of 5.69 μmol·L-1. Additionally, this compound might target the RhoGEF7 and inhibit the cellular migration by down-regulating the expression of Rac1 protein and E-cadherin protein. Then the down-regulated Rac1 protein suppressed the activation of NF-κB, which reduced the transcription of downstream genes IL-6 and IL-8. Moreover, the IL-6/JAK/STAT3 pathway was inhibited when Rac1 protein was down-regulated. CONCLUSION This study provides theoretical basis for the molecular mechanism of targeting lung cancer cells with this novel polycyclic spiro epoxidized indole compound. |
| Key words: polycyclic spiro-epoxy indole SKLU1 RhoGEF7 IL-6/JAK/STAT3 NF-κB activation |
