MicroRNA Landscape in Hepatocellular Carcinoma: Metabolic Re-Wiring, Predictive and Diagnostic Biomarkers, and Emerging Therapeutic Targets.

IF 3.9 3区 工程技术 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Dimitris Liapopoulos, Panagiotis Sarantis, Theodora Biniari, Thaleia-Eleftheria Bousou, Eleni-Myrto Trifylli, Ioanna A Anastasiou, Stefania Kokkali, Dimitra Korakaki, Spyridon Pantzios, Evangelos Koustas, Ioannis Elefsiniotis, Michalis V Karamouzis
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引用次数: 0

Abstract

Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality, in part due to late diagnosis and limited prognostic tools. In recent years, microRNAs, small, non-coding regulators of gene expression, have emerged as key modulators of tumor metabolism, microenvironmental crosstalk, and therapeutic response in HCC. This narrative review synthesizes evidence published from January 2000 through April 2025, focusing on four interrelated themes: (1) miRNA-driven metabolic rewiring; (2) circulating and exosomal miRNAs as diagnostic and (3) predictive biomarkers; (4) miRNA-based therapeutic strategies. We conducted a targeted PubMed search using terms related to HCC, miRNA biology, biomarkers, metabolism, and therapy, supplemented by manual reference mining. Preclinical and clinical studies reveal that loss of tumor-suppressor miRNAs and gain of oncomiRs orchestrate glycolysis, lipid and glutamine metabolism, and stromal-immune remodeling. Circulating miRNA signatures, including single- and multimarker panels, demonstrate diagnostic AUCs up to 0.99 for early-stage HCC and distinguish HCC from cirrhosis more accurately than alpha-fetoprotein. Predictively, miRNAs such as miR-21 and miR-486-3p correlate with sorafenib resistance, while tissue and exosomal miRNAs forecast recurrence and survival after curative therapy. Therapeutic manipulation, restoring tumor-suppressor miRNAs via mimics or AAV vectors and inhibiting oncomiRs with antagomirs or LNA oligonucleotides, yields potent anti-tumor effects in models, affecting cell cycle, apoptosis, angiogenesis, and immune activation. Despite technical and delivery challenges, early-phase trials validate target engagement and inform safety optimization. In this review, we highlight opportunities to integrate miRNA biomarkers into surveillance algorithms and combine miRNA therapeutics with existing modalities, charting a roadmap toward precision-guided management of HCC.

Abstract Image

肝细胞癌中的MicroRNA景观:代谢重新布线,预测和诊断生物标志物,以及新兴的治疗靶点。
肝细胞癌(HCC)仍然是癌症相关死亡的主要原因,部分原因是诊断较晚和预后工具有限。近年来,microrna,一种小的、非编码的基因表达调节因子,已成为HCC中肿瘤代谢、微环境串扰和治疗反应的关键调节因子。本文综合了2000年1月至2025年4月期间发表的证据,重点关注四个相互关联的主题:(1)mirna驱动的代谢重布线;(2)循环和外泌体mirna作为诊断和(3)预测性生物标志物;(4)基于mirna的治疗策略。我们使用与HCC、miRNA生物学、生物标志物、代谢和治疗相关的术语进行了有针对性的PubMed搜索,并辅以人工参考文献挖掘。临床前和临床研究表明,肿瘤抑制mirna的缺失和肿瘤抑制剂的获得协调糖酵解、脂质和谷氨酰胺代谢以及基质免疫重塑。循环miRNA特征,包括单标记和多标记面板,显示早期HCC的诊断auc高达0.99,并且比甲胎蛋白更准确地区分HCC和肝硬化。可预测的是,miR-21和miR-486-3p等mirna与索拉非尼耐药相关,而组织和外泌体mirna预测治愈性治疗后的复发和生存。治疗操作,通过模拟物或AAV载体恢复肿瘤抑制mirna,用拮抗剂或LNA寡核苷酸抑制肿瘤,在模型中产生有效的抗肿瘤作用,影响细胞周期、凋亡、血管生成和免疫激活。尽管存在技术和交付方面的挑战,但早期试验验证了目标接触,并为安全优化提供了信息。在这篇综述中,我们强调了将miRNA生物标志物整合到监测算法中的机会,并将miRNA治疗方法与现有方法相结合,为HCC的精确指导管理绘制了路线图。
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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来源期刊
Biomedicines
Biomedicines Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
5.20
自引率
8.50%
发文量
2823
审稿时长
8 weeks
期刊介绍: Biomedicines (ISSN 2227-9059; CODEN: BIOMID) is an international, scientific, open access journal on biomedicines published quarterly online by MDPI.
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