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[非小细胞肺癌来源的外泌体环状RNA circEZH2通过调控miR-495-3p/TPD52轴和NF-κB通路激活成纤维细胞]

[Non-small cell lung cancer-derived exosomal circular RNA circEZH2 activates fibroblasts by regulating the miR-495-3p / TPD52 axis and NF-κB pathway].

作者信息

Xing J, Chen L P, Yu W J

机构信息

Medical School of Ningbo University, Ningbo315000, China.

Department of Respiratory and Critical Care Medicine, the Affiliated People's Hospital of Ningbo University, Ningbo315000, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2024 Dec 23;46(12):1176-1186. doi: 10.3760/cma.j.cn112152-20230717-00015.

Abstract

To study the effects and mechanisms of activation of human lung fibroblasts (MRC-5) by exosomal RNA hsa _ circ _ 0006357 (circEZH2) derived from non-small cell lung cancer. Western blot was used to detect exosome molecular markers, reverse transcription-quantitative real-time polymerase chain reaction (RT-qPCR) and cell invasion assays to detect the effect of non-small cell lung cancer-derived exosomes on MRC-5 activation. A circRNA microarray analysis was performed in serum exosomes from patients with non-small cell lung cancer (collected at Ningbo University People's Hospital, September 2023), and levels of circEZH2 were measured in serum exosomes from non-small cell lung cancer by RT-qPCR analysis. The effects of circEZH2 on MRC-5 activation were explored using wound healing assays, Transwell assays, RT-qPCR, cellular immunofluorescence, and western blot. The regulatory effect of circEZH2 on miR-495-3p/TPD52 axis and NF-κB pathway through dual-luciferase assay, immunofluorescence, and western blot. Exosomes derived from non-small cell lung cancer cells were shown to promote MRC-5 cell invasiveness, the number of cells invaded in co-culture with exosomes derived from normal human bronchial epithelial cells was (42±5), and the number of cells invaded in co-culture with exosomes derived from non-small cell lung cancer cells (SPC-A1, H1299, A549 cells) was (246±7), (89±4), (69±14), expression of markers of fibroblast activation (α-SMA, FAP), and cytokines (IL-6, IL-8, <0.05). CircEZH2 expression was significantly upregulated in the serum exosomes of non-small cell lung cancer (<0.01). Alternatively, co-culture of exosomes derived from non-small cell lung cancer cells with MRC-5 cells promoted circEZH2 expression (<0.05). Functionally, overexpression of circEZH2 promoted MRC-5 cell migration and invasion [the cell migration rates were (30.81±2.54)% and (60.29±8.34)%, respectively, and the cell invasion numbers were (48.00±13.58) and (115.00±9.50), respectively, <0.05]. RT-qPCR, western blot, and immunofluorescence assays demonstrated a significant increase in the expression of the pro-inflammatory genes IL-6 and IL-8 in MRC-5 cells as well as the activation markers α-SMA and FAP in fibroblasts (<0.05) following the expression of circEZH2. Mechanistically, circEZH2 may function as ceRNA to regulate miR-495-3p, promote the expression of TPD52, and activate the NF-κB pathway to promote the activation of MRC-5. Exosomal circEZH2, derived from non-small cell lung cancer, may promote the activation of fibroblasts by activating the NF-κB pathway through the miR-495-3p/TPD52 axis.

摘要

研究非小细胞肺癌来源的外泌体RNA hsa_circ_0006357(circEZH2)对人肺成纤维细胞(MRC-5)的激活作用及其机制。采用蛋白质免疫印迹法检测外泌体分子标志物,逆转录-定量实时聚合酶链反应(RT-qPCR)和细胞侵袭实验检测非小细胞肺癌来源的外泌体对MRC-5激活的影响。对非小细胞肺癌患者(于2023年9月在宁波大学人民医院采集)的血清外泌体进行环状RNA微阵列分析,并通过RT-qPCR分析检测非小细胞肺癌血清外泌体中circEZH2的水平。采用伤口愈合实验、Transwell实验、RT-qPCR、细胞免疫荧光和蛋白质免疫印迹法探究circEZH2对MRC-5激活的影响。通过双荧光素酶实验、免疫荧光和蛋白质免疫印迹法检测circEZH2对miR-495-3p/TPD52轴和NF-κB通路的调控作用。结果显示,非小细胞肺癌细胞来源的外泌体可促进MRC-5细胞侵袭,与正常人支气管上皮细胞来源的外泌体共培养时侵袭的细胞数为(42±5),与非小细胞肺癌细胞(SPC-A1、H1299、A549细胞)来源的外泌体共培养时侵袭的细胞数分别为(246±7)、(89±4)、(69±14),成纤维细胞激活标志物(α-SMA、FAP)及细胞因子(IL-6、IL-8)的表达差异均有统计学意义(P<0.05)。非小细胞肺癌血清外泌体中circEZH2表达显著上调(P<0.01)。此外,非小细胞肺癌细胞来源的外泌体与MRC-5细胞共培养可促进circEZH2表达(P<0.05)。功能上,circEZH2过表达促进MRC-5细胞迁移和侵袭[细胞迁移率分别为(30.81±2.54)%和(60.29±8.34)%,细胞侵袭数分别为(48.00±13.58)和(115.00±9.50),P<0.05]。RT-qPCR、蛋白质免疫印迹和免疫荧光实验表明,circEZH2表达后MRC-5细胞中促炎基因IL-6和IL-8的表达以及成纤维细胞中激活标志物α-SMA和FAP均显著增加(P<0.05)。机制上,circEZH2可能作为竞争性内源RNA调节miR-495-3p,促进TPD52表达,并激活NF-κB通路以促进MRC-5激活。非小细胞肺癌来源的外泌体circEZH2可能通过miR-495-3p/TPD52轴激活NF-κB通路促进成纤维细胞激活。

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