• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

解读微小RNA在肝细胞癌中的多方面作用:整合文献综述与生物信息学分析以获取治疗见解

Deciphering the multifaceted role of microRNAs in hepatocellular carcinoma: Integrating literature review and bioinformatics analysis for therapeutic insights.

作者信息

Rahdan Fereshteh, Saberi Alihossein, Saraygord-Afshari Neda, Hadizadeh Morteza, Fayeghi Tahura, Ghanbari Elham, Dianat-Moghadam Hassan, Alizadeh Effat

机构信息

Department of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Medical Genetics, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

Heliyon. 2024 Oct 18;10(20):e39489. doi: 10.1016/j.heliyon.2024.e39489. eCollection 2024 Oct 30.

DOI:10.1016/j.heliyon.2024.e39489
PMID:39498055
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11532857/
Abstract

Hepatocellular carcinoma (HCC) poses a significant global health challenge, necessitating innovative therapeutic strategies. MicroRNAs (miRNAs) have emerged as pivotal regulators of HCC pathogenesis, influencing key processes such as self-renewal, angiogenesis, glycolysis, autophagy, and metastasis. This article integrates findings from a comprehensive literature review and bioinformatics analysis to elucidate the role of miRNAs in HCC. We discuss how dysregulation of miRNAs can drive HCC initiation, progression, and metastasis by modulating various signaling pathways and target genes. Moreover, leveraging high-throughput technology and bioinformatics tools, we identify key miRNAs involved in multiple cancer hallmarks, offering insights into potential combinatorial therapeutic strategies. Through our analysis considering p-values and signaling pathways associated with key features, we unveil miRNAs with simultaneous roles across critical cancer characteristics, providing a basis for the development of high-performance biomarkers. The microRNAs, miR-34a-5p, miR-373-3p, miR-21-5p, miR-214-5p, miR-195-5p, miR-139-5p were identified to be shared microRNAs in stemness, angiogenesis, glycolysis, autophagy, EMT, and metastasis of HCC. However, challenges such as miRNA stability and delivery hinder the translation of miRNA-based therapeutics into clinical practice. This review underscores the importance of further research to overcome existing barriers and realize the full potential of miRNA-based interventions for HCC management.

摘要

肝细胞癌(HCC)对全球健康构成了重大挑战,因此需要创新的治疗策略。微小RNA(miRNA)已成为HCC发病机制的关键调节因子,影响自我更新、血管生成、糖酵解、自噬和转移等关键过程。本文整合了全面的文献综述和生物信息学分析结果,以阐明miRNA在HCC中的作用。我们讨论了miRNA的失调如何通过调节各种信号通路和靶基因来驱动HCC的起始、进展和转移。此外,利用高通量技术和生物信息学工具,我们确定了参与多种癌症特征的关键miRNA,为潜在的联合治疗策略提供了见解。通过我们考虑与关键特征相关的p值和信号通路的分析,我们揭示了在关键癌症特征中具有同时作用的miRNA,为开发高性能生物标志物提供了基础。已确定微小RNA miR-34a-5p、miR-373-3p、miR-21-5p、miR-214-5p、miR-195-5p、miR-139-5p是HCC干性、血管生成、糖酵解、自噬、上皮-间质转化和转移中的共享微小RNA。然而,诸如miRNA稳定性和递送等挑战阻碍了基于miRNA的疗法转化为临床实践。本综述强调了进一步研究以克服现有障碍并实现基于miRNA的干预措施在HCC管理中的全部潜力的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/4d8fe581405e/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/e28ec5858916/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/6e2a0ceadb75/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/c061e5bc613b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/7d183866bf54/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/19f0a722f938/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/69937efb121c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/40d3129d76e4/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/ab7a2a97df49/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/4d8fe581405e/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/e28ec5858916/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/6e2a0ceadb75/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/c061e5bc613b/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/7d183866bf54/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/19f0a722f938/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/69937efb121c/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/40d3129d76e4/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/ab7a2a97df49/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d7/11532857/4d8fe581405e/gr9.jpg

相似文献

1
Deciphering the multifaceted role of microRNAs in hepatocellular carcinoma: Integrating literature review and bioinformatics analysis for therapeutic insights.解读微小RNA在肝细胞癌中的多方面作用:整合文献综述与生物信息学分析以获取治疗见解
Heliyon. 2024 Oct 18;10(20):e39489. doi: 10.1016/j.heliyon.2024.e39489. eCollection 2024 Oct 30.
2
Co-expression of miRNA players in advanced laryngeal carcinoma - Insights into the roles of miR-93-5p, miR-145-5p, and miR-210-3p.晚期喉癌中miRNA相关因子的共表达——对miR-93-5p、miR-145-5p和miR-210-3p作用的深入了解
Biomol Biomed. 2025 Apr 3;25(5):1052-1062. doi: 10.17305/bb.2024.10947.
3
Expression of LC3A, LC3B and p62/SQSTM1 autophagy proteins in hepatocellular carcinoma (HCC) tissues and the predicted microRNAs involved in the autophagy-related pathway.LC3A、LC3B 和 p62/SQSTM1 自噬蛋白在肝细胞癌 (HCC) 组织中的表达及自噬相关通路中涉及的预测 microRNAs。
J Mol Histol. 2024 Jun;55(3):317-328. doi: 10.1007/s10735-024-10191-8. Epub 2024 Apr 17.
4
The miR-561-5p/CXCL1 Signaling Axis Regulates Pulmonary Metastasis in Hepatocellular Carcinoma Involving CXCR1 Natural Killer Cells Infiltration.miR-561-5p/CXCL1 信号轴调控涉及 CXCR1 自然杀伤细胞浸润的肝细胞癌肺转移
Theranostics. 2019 Jul 9;9(16):4779-4794. doi: 10.7150/thno.32543. eCollection 2019.
5
Transcription Factors and Methylation Drive Prognostic miRNA Dysregulation in Hepatocellular Carcinoma.转录因子和甲基化驱动肝细胞癌中预后性微小RNA的失调
Front Oncol. 2021 Jul 1;11:691115. doi: 10.3389/fonc.2021.691115. eCollection 2021.
6
MiR-425-5p promotes invasion and metastasis of hepatocellular carcinoma cells through SCAI-mediated dysregulation of multiple signaling pathways.微小RNA-425-5p通过SCAI介导的多种信号通路失调促进肝癌细胞的侵袭和转移。
Oncotarget. 2017 May 9;8(19):31745-31757. doi: 10.18632/oncotarget.15958.
7
The Protective Role of miR-125b in Hepatocellular Carcinoma: Unraveling Tumor-Suppressive Mechanisms.miR-125b在肝细胞癌中的保护作用:揭示肿瘤抑制机制
Curr Mol Med. 2024 Jun 7. doi: 10.2174/0115665240304247240529074123.
8
MicroRNA-876-5p inhibits epithelial-mesenchymal transition and metastasis of hepatocellular carcinoma by targeting BCL6 corepressor like 1.miR-876-5p 通过靶向 BCL6 共抑制因子样 1 抑制肝癌的上皮-间充质转化和转移。
Biomed Pharmacother. 2018 Jul;103:645-652. doi: 10.1016/j.biopha.2018.04.037. Epub 2018 Apr 24.
9
miR-296-5p suppresses EMT of hepatocellular carcinoma via attenuating NRG1/ERBB2/ERBB3 signaling.miR-296-5p 通过抑制 NRG1/ERBB2/ERBB3 信号通路抑制肝癌 EMT。
J Exp Clin Cancer Res. 2018 Nov 29;37(1):294. doi: 10.1186/s13046-018-0957-2.
10
MicroRNA-379-5p inhibits tumor invasion and metastasis by targeting FAK/AKT signaling in hepatocellular carcinoma.微小RNA-379-5p通过靶向肝细胞癌中的FAK/AKT信号传导抑制肿瘤侵袭和转移。
Cancer Lett. 2016 May 28;375(1):73-83. doi: 10.1016/j.canlet.2016.02.043. Epub 2016 Mar 2.

引用本文的文献

1
Breaking the oncogenic alliance: advances in disrupting the MTDH-SND1 complex for cancer therapy.打破致癌联盟:破坏MTDH-SND1复合物用于癌症治疗的研究进展
RSC Adv. 2025 Aug 26;15(37):30165-30188. doi: 10.1039/d5ra04310g. eCollection 2025 Aug 22.
2
MicroRNA‑885‑5p regulates cell cycle progression in liver cancer cells.微小RNA-885-5p调节肝癌细胞的细胞周期进程。
Int J Mol Med. 2025 Nov;56(5). doi: 10.3892/ijmm.2025.5608. Epub 2025 Aug 14.
3
Non-coding RNAs as key regulators in hepatitis B virus-related hepatocellular carcinoma.

本文引用的文献

1
miRNA-Based Technologies in Cancer Therapy.癌症治疗中基于微小RNA的技术
J Pers Med. 2023 Nov 9;13(11):1586. doi: 10.3390/jpm13111586.
2
Low-dose radiotherapy combined with dual PD-L1 and VEGFA blockade elicits antitumor response in hepatocellular carcinoma mediated by activated intratumoral CD8 exhausted-like T cells.低剂量放疗联合双重 PD-L1 和 VEGFA 阻断通过激活肿瘤内耗尽样 CD8 T 细胞介导的肝细胞癌的抗肿瘤反应。
Nat Commun. 2023 Nov 24;14(1):7709. doi: 10.1038/s41467-023-43462-1.
3
MicroRNAs and their vital role in apoptosis in hepatocellular carcinoma: miRNA-based diagnostic and treatment methods.
非编码RNA作为乙型肝炎病毒相关肝细胞癌的关键调节因子
Front Immunol. 2025 Jun 23;16:1602252. doi: 10.3389/fimmu.2025.1602252. eCollection 2025.
4
Molecular mechanisms and therapeutic strategies in overcoming chemotherapy resistance in cancer.癌症中克服化疗耐药性的分子机制与治疗策略
Mol Biomed. 2025 Jan 6;6(1):2. doi: 10.1186/s43556-024-00239-2.
微小 RNA 及其在肝细胞癌细胞凋亡中的重要作用:基于微小 RNA 的诊断和治疗方法。
Gene. 2023 Dec 20;888:147803. doi: 10.1016/j.gene.2023.147803. Epub 2023 Sep 14.
4
Endoplasmic reticulum stress: molecular mechanism and therapeutic targets.内质网应激:分子机制与治疗靶点。
Signal Transduct Target Ther. 2023 Sep 15;8(1):352. doi: 10.1038/s41392-023-01570-w.
5
Chitosan-Based Nanoparticles for Nucleic Acid Delivery: Technological Aspects, Applications, and Future Perspectives.用于核酸递送的壳聚糖基纳米颗粒:技术层面、应用及未来展望
Pharmaceutics. 2023 Jun 29;15(7):1849. doi: 10.3390/pharmaceutics15071849.
6
miRNAs: Potential as Biomarkers and Therapeutic Targets for Cancer.miRNAs:癌症的潜在生物标志物和治疗靶点。
Genes (Basel). 2023 Jun 29;14(7):1375. doi: 10.3390/genes14071375.
7
MicroRNA: trends in clinical trials of cancer diagnosis and therapy strategies.微小 RNA:癌症诊断和治疗策略临床试验的趋势。
Exp Mol Med. 2023 Jul;55(7):1314-1321. doi: 10.1038/s12276-023-01050-9. Epub 2023 Jul 10.
8
Advanced HCC with amplified mesenchymal epithelial transition factor receptor responds well to savolitinib: a case report.具有间充质上皮转化因子受体扩增的晚期肝细胞癌对赛沃替尼反应良好:病例报告
Front Med (Lausanne). 2023 May 24;10:1130012. doi: 10.3389/fmed.2023.1130012. eCollection 2023.
9
Pathogenesis of Hepatocellular Carcinoma: The Interplay of Apoptosis and Autophagy.肝细胞癌的发病机制:细胞凋亡与自噬的相互作用
Biomedicines. 2023 Apr 13;11(4):1166. doi: 10.3390/biomedicines11041166.
10
Autophagy orchestrates resistance in hepatocellular carcinoma cells.自噬调控肝癌细胞的耐药性。
Biomed Pharmacother. 2023 May;161:114487. doi: 10.1016/j.biopha.2023.114487. Epub 2023 Mar 22.