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本文引用的文献

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Targeting MicroRNAs with Small Molecules.用小分子靶向微小RNA
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2
Clinical importance of serum miRNA levels in breast cancer patients.血清miRNA水平在乳腺癌患者中的临床重要性。
Discov Oncol. 2024 Jan 27;15(1):19. doi: 10.1007/s12672-024-00871-y.
3
Small molecule approaches to targeting RNA.靶向RNA的小分子方法。
Nat Rev Chem. 2024 Feb;8(2):120-135. doi: 10.1038/s41570-023-00569-9. Epub 2024 Jan 26.
4
Altering the Cleaving Effector in Chimeric Molecules that Target RNA Enhances Cellular Selectivity.改变靶向 RNA 的嵌合分子中的切割效应子可提高细胞选择性。
ACS Chem Biol. 2023 Nov 17;18(11):2385-2393. doi: 10.1021/acschembio.3c00363. Epub 2023 Oct 12.
5
Molecular docking as a tool for the discovery of molecular targets of nutraceuticals in diseases management.分子对接作为一种工具,用于发现疾病管理中营养保健品的分子靶标。
Sci Rep. 2023 Aug 17;13(1):13398. doi: 10.1038/s41598-023-40160-2.
6
Synthesis of Bleomycin-Inspired RNA Ligands Targeting the Biogenesis of Oncogenic miRNAs.合成受博来霉素启发的 RNA 配体,靶向致癌 miRNA 的生物发生。
J Med Chem. 2023 Aug 10;66(15):10639-10657. doi: 10.1021/acs.jmedchem.3c00797. Epub 2023 Jul 14.
7
RNA-targeted small-molecule drug discoveries: a machine-learning perspective.基于机器学习的靶向 RNA 小分子药物研发
RNA Biol. 2023 Jan;20(1):384-397. doi: 10.1080/15476286.2023.2223498.
8
Small-molecule discovery through DNA-encoded libraries.通过 DNA 编码文库进行小分子发现。
Nat Rev Drug Discov. 2023 Sep;22(9):699-722. doi: 10.1038/s41573-023-00713-6. Epub 2023 Jun 16.
9
Prediction of small molecule drug-miRNA associations based on GNNs and CNNs.基于图神经网络(GNNs)和卷积神经网络(CNNs)的小分子药物与微小RNA(miRNA)关联预测
Front Genet. 2023 May 30;14:1201934. doi: 10.3389/fgene.2023.1201934. eCollection 2023.
10
Targeted Degradation of Structured RNAs via Ribonuclease-Targeting Chimeras (RiboTacs).通过核糖核酸酶靶向嵌合体(RiboTacs)靶向降解结构化 RNA。
Expert Opin Drug Discov. 2023 Jul-Dec;18(8):929-942. doi: 10.1080/17460441.2023.2224960. Epub 2023 Jun 20.

靶向微小RNA的小分子:精准癌症治疗中的新机遇与挑战

Small molecules targeting microRNAs: new opportunities and challenges in precision cancer therapy.

作者信息

Jurj Ancuta, Fontana Beatrice, Varani Gabriele, Calin George A

机构信息

Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA; Department of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum University of Bologna, Bologna, Italy.

出版信息

Trends Cancer. 2024 Sep;10(9):809-824. doi: 10.1016/j.trecan.2024.06.006. Epub 2024 Aug 5.

DOI:10.1016/j.trecan.2024.06.006
PMID:39107162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11961049/
Abstract

Noncoding RNAs, especially miRNAs, play a pivotal role in cancer initiation and metastasis, underscoring their susceptibility to precise modulation via small molecule inhibitors. This review examines the innovative strategy of targeting oncogenic miRNAs with small drug-like molecules, an approach that can reshape the cancer treatment landscape. We review the current understanding of the multifaceted roles of miRNAs in oncogenesis, highlighting emerging therapeutic paradigms that have the potential to expand cancer treatment options. As research on small molecule inhibitors of miRNA is still in its early stages, ongoing investigative efforts and the development of new technologies and chemical matter are essential to fulfill the significant potential of this innovative approach to cancer treatment.

摘要

非编码RNA,尤其是微小RNA(miRNA),在癌症的发生和转移中起着关键作用,这突出了它们对通过小分子抑制剂进行精确调控的敏感性。本综述探讨了用类药物小分子靶向致癌miRNA的创新策略,这种方法能够重塑癌症治疗格局。我们回顾了目前对miRNA在肿瘤发生中多方面作用的理解,强调了有可能拓展癌症治疗选择的新兴治疗模式。由于对miRNA小分子抑制剂的研究仍处于早期阶段,持续的研究工作以及新技术和化学物质的开发对于实现这种创新癌症治疗方法的巨大潜力至关重要。