miR-215-5p Plays a Key Role in Suppressing Vascular Invasion and Recurrence in Hepatocellular Carcinoma by Blocking Vasculogenic Mimicry.

Heng Zhang, Xi Lan, Liquan Cai, Xunfeng Gao, Feng Gao, Dan Yu, Jinlong Zhang, Jinhui Zhang, Qinwen Tai
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Abstract

Background: This research explores the significance of miR-215-5p and vasculogenic mimicry (VM) in forecasting the prognosis for hepatocellular carcinoma (HCC).

Methods: We analyzed HCC-associated miRNA expression profiles using data from The Cancer Genome Atlas (TCGA) and the Gene Expression Omnibus (GEO). Samples included tissue and blood from 80 early-stage HCC patients and serum from 120 healthy individuals. Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was employed to measure miR-215-5p and zinc finger E-box binding homeobox 2 (ZEB2) gene expressions. Hematoxylin and eosin (H&E) and CD34/Periodic Acid-Schiff (PAS) double staining assessed VM presence in HCC tissue sections. Bioinformatics tools predicted interactions between miR-215-5p and ZEB2, confirmed through luciferase reporter assays. We also examined the impact of miR-215-5p or ZEB2 overexpression on HCC cell invasion, migration, and VM formation using scratch, Transwell invasion assays, and Matrigel 3D cultures.

Results: Bioinformatics analysis indicated that miR-215-5p was under-expressed in HCC, particularly in cases with vascular invasion, which correlated with worse patient outcomes. In contrast, ZEB2, targeted by miR-215-5p, was overexpressed in HCC. RT-qPCR validated these expression patterns in HCC tissues. Among the HCC patients, 38 were VM positive and 42 VM negative. Logistic regression highlighted a negative correlation between miR-215-5p levels and VM positivity in HCC tissues and a positive correlation for ZEB2 with VM positivity and tumor vascular invasion. Lower miR-215-5p levels were linked to increased HCC recurrence and metastasis. Both bioinformatics analysis and luciferase assays demonstrated a direct interaction between miR-215-5p and ZEB2. Enhancing miR-215-5p levels reduced ZEB2 expression, consequently diminishing invasion, migration, and VM formation of the HCC cells in vitro.

Conclusions: miR-215-5p expression inversely correlates with VM occurrence in HCC tissues, while ZEB2 expression shows a direct correlation. By targeting ZEB2, miR-215-5p may hinder VM in HCC tissues, helping to prevent vascular invasion and HCC recurrence. Thus, miR-215-5p emerges as a vital prognostic indicator for predicting vascular invasion and recurrence in HCC.

miR-215-5p 通过阻断血管生成模拟在抑制肝细胞癌血管侵袭和复发中发挥关键作用
背景:本研究探讨了 miR-215-5p 和血管生成模拟(VM)在预测肝细胞癌(HCC)预后中的意义:本研究探讨了miR-215-5p和血管生成模拟(VM)在预测肝细胞癌(HCC)预后中的意义:我们利用癌症基因组图谱(The Cancer Genome Atlas,TCGA)和基因表达总库(Gene Expression Omnibus,GEO)的数据分析了与HCC相关的miRNA表达谱。样本包括 80 名早期 HCC 患者的组织和血液以及 120 名健康人的血清。采用逆转录-定量聚合酶链反应(RT-qPCR)测定 miR-215-5p 和锌指 E-box binding homeobox 2 (ZEB2) 基因的表达。血色素和伊红(H&E)以及CD34/Periodic Acid-Schiff (PAS)双重染色评估了HCC组织切片中VM的存在。生物信息学工具预测了 miR-215-5p 与 ZEB2 之间的相互作用,并通过荧光素酶报告实验证实了这一点。我们还使用划痕法、Transwell侵袭试验和Matrigel三维培养法检测了miR-215-5p或ZEB2过表达对HCC细胞侵袭、迁移和VM形成的影响:生物信息学分析表明,miR-215-5p在HCC中表达不足,尤其是在有血管侵犯的病例中,这与患者的预后相关。相反,miR-215-5p 的靶标 ZEB2 在 HCC 中过表达。RT-qPCR 验证了这些在 HCC 组织中的表达模式。在 HCC 患者中,38 例为 VM 阳性,42 例为 VM 阴性。逻辑回归结果显示,miR-215-5p 水平与 HCC 组织中的 VM 阳性呈负相关,而 ZEB2 与 VM 阳性和肿瘤血管侵犯呈正相关。较低的 miR-215-5p 水平与 HCC 复发和转移的增加有关。生物信息学分析和荧光素酶测定都证明了 miR-215-5p 与 ZEB2 之间的直接相互作用。结论:miR-215-5p 的表达与 HCC 组织中 VM 的发生成反比,而 ZEB2 的表达则与之直接相关。通过靶向 ZEB2,miR-215-5p 可阻碍 HCC 组织中 VM 的形成,有助于防止血管入侵和 HCC 复发。因此,miR-215-5p 是预测 HCC 血管侵犯和复发的重要预后指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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