Tianyu Lin, Xinli Guo, Qian Du, Wei Liu, Xin Zhong, Suihan Wang, Liping Cao
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Cell proliferation, migration, invasion, and apoptosis were detected by CCK-8, Wound healing, Transwell, and Flow cytometry, respectively. RT-qPCR and Western blot were used to detect the expression of let-7c-5p and EZH2.\nResults. EZH2 was upregulated in HCC tumors (P < 0.0001). Cox regression analysis showed that TCGA HCC patients with high EZH2 expression levels showed a short survival time (HR = 1.677, 95% CI 1.316-2.137; P < 0.0001). Seven miRNAs were negatively correlated with EZH2 expression and were significantly downregulated in HCC tumor samples (P < 0.0001), in which hsa-let-7c-5p was associated with prognosis in HCC (HR = 0.849 95% CI 0.739-0.975; P = 0.021). We identified 14 immune cells that showed significant differences in EZH2 high- and low- expression groups. Additionally, let-7c-5p inhibited HCC cell proliferation, migration, and invasion and reversed the promoted effects of EZH2 on HCC cell malignant characteristics.\nConclusions. hsa-let-7c-5p-EZH2 significantly suppressed HCC malignant characteristics, which can be used for HCC prognosis.","PeriodicalId":55205,"journal":{"name":"Critical Reviews in Immunology","volume":"23 1","pages":""},"PeriodicalIF":0.8000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"MicroRNA let-7c-5p Alleviates in Hepatocellular Carcinoma by Targeting Enhancer of Zeste Homolog 2: An study intersecting bioinformatic analysis and validated experiments\",\"authors\":\"Tianyu Lin, Xinli Guo, Qian Du, Wei Liu, Xin Zhong, Suihan Wang, Liping Cao\",\"doi\":\"10.1615/critrevimmunol.2024051519\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objectives. Enhancer of zeste homolog 2 (EZH2) gene has a prognostic role in hepatocellular carcinoma (HCC). This study aimed to identify the role of microRNAs (miRNAs) let-7c-5p by targeting EZH2 in HCC.\\nMethods. We downloaded gene and miRNA RNA-seq data from The Cancer Genome Atlas (TCGA) database. Differences in EZH2 expression between different groups were analyzed and the association of EZH2 expression with HCC prognosis was detected using Cox regression analysis. The miRNA-EZH2-pathway network was constructed. Dual-luciferase reporter assay was performed to detect the hsa-let-7c-5p-EZH2. Cell proliferation, migration, invasion, and apoptosis were detected by CCK-8, Wound healing, Transwell, and Flow cytometry, respectively. RT-qPCR and Western blot were used to detect the expression of let-7c-5p and EZH2.\\nResults. EZH2 was upregulated in HCC tumors (P < 0.0001). Cox regression analysis showed that TCGA HCC patients with high EZH2 expression levels showed a short survival time (HR = 1.677, 95% CI 1.316-2.137; P < 0.0001). Seven miRNAs were negatively correlated with EZH2 expression and were significantly downregulated in HCC tumor samples (P < 0.0001), in which hsa-let-7c-5p was associated with prognosis in HCC (HR = 0.849 95% CI 0.739-0.975; P = 0.021). We identified 14 immune cells that showed significant differences in EZH2 high- and low- expression groups. 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引用次数: 0
摘要
研究目的泽斯特同源增强子 2(EZH2)基因在肝细胞癌(HCC)中具有预后作用。本研究旨在确定靶向 EZH2 的 microRNA(miRNA)let-7c-5p 在 HCC 中的作用。我们从癌症基因组图谱(TCGA)数据库中下载了基因和miRNA RNA-seq数据。方法:我们从癌症基因组图谱(TCGA)数据库中下载了基因和miRNA RNA-seq数据,分析了不同组间EZH2表达的差异,并使用Cox回归分析检测了EZH2表达与HCC预后的关系。构建了miRNA-EZH2通路网络。采用双荧光素酶报告实验检测 hsa-let-7c-5p-EZH2。细胞增殖、迁移、侵袭和凋亡分别通过 CCK-8、伤口愈合、Transwell 和流式细胞术进行检测。采用 RT-qPCR 和 Western 印迹法检测 let-7c-5p 和 EZH2 的表达。EZH2在HCC肿瘤中上调(P< 0.0001)。Cox回归分析表明,EZH2高表达水平的TCGA HCC患者生存时间较短(HR = 1.677, 95% CI 1.316-2.137; P <0.0001)。7种miRNA与EZH2的表达呈负相关,并在HCC肿瘤样本中显著下调(P <0.0001),其中hsa-let-7c-5p与HCC的预后相关(HR = 0.849 95% CI 0.739-0.975; P = 0.021)。我们发现有 14 种免疫细胞在 EZH2 高表达组和低表达组中存在显著差异。此外,let-7c-5p能抑制HCC细胞的增殖、迁移和侵袭,并逆转EZH2对HCC细胞恶性特征的促进作用。
MicroRNA let-7c-5p Alleviates in Hepatocellular Carcinoma by Targeting Enhancer of Zeste Homolog 2: An study intersecting bioinformatic analysis and validated experiments
Objectives. Enhancer of zeste homolog 2 (EZH2) gene has a prognostic role in hepatocellular carcinoma (HCC). This study aimed to identify the role of microRNAs (miRNAs) let-7c-5p by targeting EZH2 in HCC.
Methods. We downloaded gene and miRNA RNA-seq data from The Cancer Genome Atlas (TCGA) database. Differences in EZH2 expression between different groups were analyzed and the association of EZH2 expression with HCC prognosis was detected using Cox regression analysis. The miRNA-EZH2-pathway network was constructed. Dual-luciferase reporter assay was performed to detect the hsa-let-7c-5p-EZH2. Cell proliferation, migration, invasion, and apoptosis were detected by CCK-8, Wound healing, Transwell, and Flow cytometry, respectively. RT-qPCR and Western blot were used to detect the expression of let-7c-5p and EZH2.
Results. EZH2 was upregulated in HCC tumors (P < 0.0001). Cox regression analysis showed that TCGA HCC patients with high EZH2 expression levels showed a short survival time (HR = 1.677, 95% CI 1.316-2.137; P < 0.0001). Seven miRNAs were negatively correlated with EZH2 expression and were significantly downregulated in HCC tumor samples (P < 0.0001), in which hsa-let-7c-5p was associated with prognosis in HCC (HR = 0.849 95% CI 0.739-0.975; P = 0.021). We identified 14 immune cells that showed significant differences in EZH2 high- and low- expression groups. Additionally, let-7c-5p inhibited HCC cell proliferation, migration, and invasion and reversed the promoted effects of EZH2 on HCC cell malignant characteristics.
Conclusions. hsa-let-7c-5p-EZH2 significantly suppressed HCC malignant characteristics, which can be used for HCC prognosis.
期刊介绍:
Immunology covers a broad spectrum of investigations at the genes, molecular, cellular, organ and system levels to reveal defense mechanisms against pathogens as well as protection against tumors and autoimmune diseases. The great advances in immunology in recent years make this field one of the most dynamic and rapidly growing in medical sciences. Critical ReviewsTM in Immunology (CRI) seeks to present a balanced overview of contemporary adaptive and innate immune responses related to autoimmunity, tumor, microbe, transplantation, neuroimmunology, immune regulation and immunotherapy from basic to translational aspects in health and disease. The articles that appear in CRI are mostly obtained by invitations to active investigators. But the journal will also consider proposals from the scientific community. Interested investigators should send their inquiries to the editor before submitting a manuscript.