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非编码 RNA 疗法在早期临床试验中的系统评价:针对癌症的新视角。

A systematic review of non-coding RNA therapeutics in early clinical trials: a new perspective against cancer.

机构信息

Department of Experimental and Clinical Medicine, Magna Graecia University, Catanzaro, Italy.

出版信息

J Transl Med. 2024 Aug 5;22(1):731. doi: 10.1186/s12967-024-05554-4.


DOI:10.1186/s12967-024-05554-4
PMID:39103911
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11301835/
Abstract

Targeting non-coding RNAs (ncRNAs), including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), has recently emerged as a promising strategy for treating malignancies and other diseases. In recent years, the development of ncRNA-based therapeutics for targeting protein-coding and non-coding genes has also gained momentum. This review systematically examines ongoing and completed clinical trials to provide a comprehensive overview of the emerging landscape of ncRNA-based therapeutics. Significant efforts have been made to advance ncRNA therapeutics to early clinical studies. The most advanced trials have been conducted with small interfering RNAs (siRNAs), miRNA replacement using nanovector-entrapped miRNA mimics, or miRNA silencing by antisense oligonucleotides. While siRNA-based therapeutics have already received FDA approval, miRNA mimics, inhibitors, and lncRNA-based therapeutics are still under evaluation in preclinical and early clinical studies. We critically discuss the rationale and methodologies of ncRNA targeting strategies to illustrate this rapidly evolving field.

摘要

靶向非编码 RNA(ncRNAs),包括 microRNAs(miRNAs)和长非编码 RNA(lncRNAs),最近已成为治疗恶性肿瘤和其他疾病的一种有前途的策略。近年来,基于 ncRNA 的治疗方法也在针对蛋白质编码和非编码基因方面取得了进展。本综述系统地检查了正在进行和已完成的临床试验,以提供 ncRNA 治疗的新兴领域的全面概述。已经做出了重大努力将 ncRNA 治疗推进到早期临床研究。最先进的试验是使用小干扰 RNA(siRNA)、纳米载体包裹的 miRNA 模拟物进行 miRNA 替代,或通过反义寡核苷酸进行 miRNA 沉默进行的。虽然基于 siRNA 的治疗方法已经获得 FDA 批准,但 miRNA 模拟物、抑制剂和 lncRNA 治疗方法仍在临床前和早期临床研究中进行评估。我们批判性地讨论了 ncRNA 靶向策略的原理和方法,以说明这个快速发展的领域。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/fd9c2745ad5f/12967_2024_5554_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/158affe59e27/12967_2024_5554_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/ffaf8f22c124/12967_2024_5554_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/fd9c2745ad5f/12967_2024_5554_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/158affe59e27/12967_2024_5554_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/ffaf8f22c124/12967_2024_5554_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b3/11301835/fd9c2745ad5f/12967_2024_5554_Fig3_HTML.jpg

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本文引用的文献

[1]
LNA-i-miR-221 activity in colorectal cancer: A reverse translational investigation.

Mol Ther Nucleic Acids. 2024-5-20

[2]
Comprehensive characterization of stemness-related lncRNAs in triple-negative breast cancer identified a novel prognostic signature related to treatment outcomes, immune landscape analysis and therapeutic guidance: a silico analysis with in vivo experiments.

J Transl Med. 2024-5-4

[3]
Therapeutic efficacy of a novel self-assembled immunostimulatory siRNA combining apoptosis promotion with RIG-I activation in gliomas.

J Transl Med. 2024-4-29

[4]
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Nat Rev Drug Discov. 2024-2

[5]
Hsa_circ_0136666 stimulates gastric cancer progression and tumor immune escape by regulating the miR-375/PRKDC Axis and PD-L1 phosphorylation.

Mol Cancer. 2023-12-13

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Targeting long non-coding RNAs in cancer therapy using CRISPR-Cas9 technology: A novel paradigm for precision oncology.

J Biotechnol. 2024-1-10

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Antisense oligonucleotides: a novel Frontier in pharmacological strategy.

Front Pharmacol. 2023-11-17

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The Emerging Roles of Exosomal miRNAs in Breast Cancer Progression and Potential Clinical Applications.

Breast Cancer (Dove Med Press). 2023-11-16

[9]
Non-coding RNAs in disease: from mechanisms to therapeutics.

Nat Rev Genet. 2024-3

[10]
Targeting non-coding RNAs: Perspectives and challenges of in-silico approaches.

Eur J Med Chem. 2023-12-5

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