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中国精品科技期刊2020
崔明辉,张奇,陈俊颖,等. 基于转录后调控筛选蛹虫草靶向作用egfr的miRNAJ. 食品工业科技,2026,47(8):1−10. doi: 10.13386/j.issn1002-0306.2025040012.
引用本文: 崔明辉,张奇,陈俊颖,等. 基于转录后调控筛选蛹虫草靶向作用egfr的miRNAJ. 食品工业科技,2026,47(8):1−10. doi: 10.13386/j.issn1002-0306.2025040012.
CUI Minghui, ZHANG Qi, CHEN Junying, et al. Investigating the Post-Transcriptional Regulation of egfr in Non-Small Cell Lung Cancer A549 Cells by Cordyceps militaris Based on miRNAJ. Science and Technology of Food Industry, 2026, 47(8): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040012.
Citation: CUI Minghui, ZHANG Qi, CHEN Junying, et al. Investigating the Post-Transcriptional Regulation of egfr in Non-Small Cell Lung Cancer A549 Cells by Cordyceps militaris Based on miRNAJ. Science and Technology of Food Industry, 2026, 47(8): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025040012.

基于转录后调控筛选蛹虫草靶向作用egfr的miRNA

Investigating the Post-Transcriptional Regulation of egfr in Non-Small Cell Lung Cancer A549 Cells by Cordyceps militaris Based on miRNA

  • 摘要: 目的:旨在获得蛹虫草抗肿瘤机制中转录后靶向调控egfr的miRNA。方法:通过水浴浸提结合真空冷冻干燥技术制备蛹虫草水提物。4 mg/mL蛹虫草处理A549细胞24 h后转录组测序,根据KEGG通路富集分析结果获得候选miRNAs。瞬时转染miRNA mimics构建功能获得模型,MTT法及Annexin V-FITC/PI双染法检测miRNAs对细胞活力的影响。同时,采用瞬时转染miRNA inhibitor构建功能缺失模型,联用蛹虫草提取物处理,MTT法检测蛹虫草-miRNA轴对细胞活力的影响,qRT-PCR和免疫细胞化学染色法分析该调控轴对A549细胞EGFR转录水平和蛋白水平的影响。结果:共获得7211个DEGs,并在“MicroRNAs in cancer”信号通路显著富集(排序3)。筛选到与肺腺癌预后相关的miRNAs共11个,其中6个与egfr存在靶向调控关系,且低表达水平的肺腺癌患者预后较差(P<0.05)。蛹虫草处理可诱导miR-125b-1-3p、miR-125b-5p和miR-145-5p表达水平显著上调(P<0.01),且种子序列与egfr 3'UTR区存在潜在结合位点。3个miRNAs的促增殖活性具有肿瘤特异性,高表达状态可诱导A549细胞发生更高比例的早期凋亡。蛹虫草可通过促进miR-125b-1-3p、miR-125b-5p和miR-145-5p的表达(P<0.05),靶向下调EGRF蛋白的表达(P<0.05),抑制肺癌A549细胞的增殖。结论:蛹虫草具有靶向调控miRNAs(miR-125b-1-3p、miR-125b-5p和miR-145-5p)-EGFR轴的抗肿瘤活性,本研究为蛹虫草开发为辅助肿瘤治疗的功能性食品提供了理论支撑。

     

    Abstract: Objective: The aim of this study was to identify miRNAs that post-transcriptionally target the regulation of egfr in the antitumor mechanism of Cordyceps militaris. Methods: An aqueous extract of Cordyceps militaris was prepared using water-bath extraction combined with vacuum freeze-drying. Transcriptome sequencing was performed on A549 cells after 24 h treatment with 4 mg/mL Cordyceps militaris extract. Candidate miRNAs were selected on the basis of Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis. Functional gain models were constructed by transient transfection of miRNA mimics, and the effects of miRNAs on cell viability were assessed using the MTT assay and Annexin V-FITC/PI double staining. Functional loss models were established by transient transfection of miRNA inhibitors, in combination with Cordyceps militaris extract treatment. The effect of Cordyceps-miRNA axis on cell viability was evaluated using the MTT assay, and its regulatory effects on EGFR transcription and protein levels in A549 cells were analyzed using qRT-PCR and immunocytochemical staining. Results: A total of 7211 DEGs were obtained and significantly enriched in the “MicroRNAs in cancer” signaling pathway (Sort 3). Eleven miRNAs were screened for their association with lung adenocarcinoma prognosis, miR-125a-3p, miR-125a-5p, miR-125b-1-3p, miR-125b-2-3p, miR-125b-5p and miR-145-5p were all associated with egfr in a target-regulatory manner, and patients with lung adenocarcinomas that showed low expression levels had a poorer prognosis (P<0.05). Cordyceps militaris treatment induced significant upregulation of miR-125b-1-3p, miR-125b-5p and miR-145-5p expression levels (P<0.01), and the seed sequences had potential binding sites with the egfr 3′-UTR region. miR-125b-1-3p, miR-125b-5p, and miR-145-5p exhibited tumor-specific pro-proliferative activities, and their high expression status induced a higher percentage of early apoptosis in A549 cells. Cordyceps militaris inhibited the proliferation of lung cancer A549 cells by promoting the expression of miR-125b-1-3p, miR-125b-5p, and miR-145-5p (P<0.05) and downregulating the expression of EGRF (P<0.05). Conclusion: Cordyceps militaris exerts anti-tumor activity by targeting and regulating the miRNAs (miR-125b-1-3p, miR-125b-5p and miR-145-5p)-EGFR axis, providing theoretical support for its development as a novel functional food for adjuvant tumor therapy.

     

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