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纳米载体介导的 microRNAs 递送至纤维性疾病。

Nanocarrier-Mediated Delivery of MicroRNAs for Fibrotic Diseases.

机构信息

Yunnan Key Laboratory of Stem Cell and Regenerative Medicine, Science and Technology Achievement Incubation Center, NHC Key Laboratory of Drug Addiction Medicine, Kunming Medical University, 1168 West Chunrong Road, Yuhua Avenue, Chenggong District, Kunming, 650500, Yunnan, China.

Department of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, Kunming Medical University, Kunming, 650106, Yunnan, China.

出版信息

Mol Diagn Ther. 2024 Jan;28(1):53-67. doi: 10.1007/s40291-023-00681-y. Epub 2023 Oct 28.


DOI:10.1007/s40291-023-00681-y
PMID:37897655
Abstract

MicroRNAs (miRNAs) are endogenous noncoding RNAs that mediate the fibrotic process by regulating multiple targets. MicroRNA-based therapy can restore or inhibit miRNA expression and is expected to become an effective approach to prevent and alleviate fibrotic diseases. However, the safe, targeted, and effective delivery of miRNAs is a major challenge in translating miRNA therapy from bench to bedside. In this review, we briefly describe the pathophysiological process of fibrosis and the mechanism by which miRNAs regulate the progression of fibrosis. Additionally, we summarize the miRNA nanodelivery tools for fibrotic diseases, including chemical modifications and polymer-based, lipid-based, and exosome-based delivery systems. Further clarification of the role of miRNAs in fibrosis and the development of a novel nanodelivery system may facilitate the prevention and alleviation of fibrotic diseases in the future.

摘要

微小 RNA(miRNA)是内源性非编码 RNA,通过调节多个靶标来介导纤维化过程。基于 miRNA 的治疗可以恢复或抑制 miRNA 的表达,有望成为预防和减轻纤维化疾病的有效方法。然而,miRNA 的安全、靶向和有效传递是将 miRNA 治疗从实验室转化到临床的主要挑战。在这篇综述中,我们简要描述了纤维化的病理生理过程以及 miRNA 调节纤维化进展的机制。此外,我们总结了用于纤维化疾病的 miRNA 纳米递药工具,包括化学修饰以及基于聚合物、基于脂质和基于外泌体的递药系统。进一步阐明 miRNA 在纤维化中的作用以及开发新型纳米递药系统可能有助于未来预防和减轻纤维化疾病。

相似文献

[1]
Nanocarrier-Mediated Delivery of MicroRNAs for Fibrotic Diseases.

Mol Diagn Ther. 2024-1

[2]
MicroRNA-21: a central regulator of fibrotic diseases via various targets.

Curr Pharm Des. 2015

[3]
MicroRNAs-mediated epithelial-mesenchymal transition in fibrotic diseases.

Eur J Pharmacol. 2017-2-5

[4]
MicroRNA in Fibrotic Disorders: A Potential Target for Future Therapeutics.

Front Biosci (Landmark Ed). 2023-11-29

[5]
MicroRNA-29: a potential therapeutic target for systemic sclerosis.

Expert Opin Ther Targets. 2012-7-16

[6]
MicroRNA-145-5p regulates fibrotic features of recessive dystrophic epidermolysis bullosa skin fibroblasts.

Br J Dermatol. 2019-11

[7]
The role of microRNAs in skin fibrosis.

Arch Dermatol Res. 2013-11

[8]
Role of MicroRNAs in TGF-β Signaling Pathway-Mediated Pulmonary Fibrosis.

Int J Mol Sci. 2017-11-25

[9]
Delivery of therapeutic miRNA using polymer-based formulation.

Drug Deliv Transl Res. 2019-12

[10]
Searching for airways biomarkers useful to identify progressive pulmonary fibrosis.

BMC Pulm Med. 2023-10-26

本文引用的文献

[1]
SMAD4 endows TGF-β1-induced highly invasive tumor cells with ferroptosis vulnerability in pancreatic cancer.

Acta Pharmacol Sin. 2024-4

[2]
Correction to: Reduced regulatory effects of bone marrow-derived mesenchymal stem cells on activated T lymphocytes and Th1/Th2 cytokine secretion in children with aplastic anemia.

Clin Exp Med. 2023-12

[3]
NRF2 is essential for iron-overload stimulated osteoclast differentiation through regulation of redox and iron homeostasis.

Cell Biol Toxicol. 2023-12

[4]
Exosomal miR-17-5p from human embryonic stem cells prevents pulmonary fibrosis by targeting thrombospondin-2.

Stem Cell Res Ther. 2023-9-4

[5]
Hepatocyte-derived exosomal miR-146a-5p inhibits hepatic stellate cell EMT process: a crosstalk between hepatocytes and hepatic stellate cells.

Cell Death Discov. 2023-8-19

[6]
Exosomal MiR-381 from M2-polarized macrophages attenuates urethral fibroblasts activation through YAP/GLS1-regulated glutaminolysis.

Inflamm Res. 2023-7

[7]
Bone marrow mesenchymal stem cell-derived exosomes alleviate skin fibrosis in systemic sclerosis by inhibiting the IL-33/ST2 axis via the delivery of microRNA-214.

Mol Immunol. 2023-5

[8]
Adipose-derived mesenchymal stem cells-sourced exosomal microRNA-7846-3p suppresses proliferation and pro-angiogenic role of keloid fibroblasts by suppressing neuropilin 2.

J Cosmet Dermatol. 2023-8

[9]
Microneedle Patch Loaded with Exosomes Containing MicroRNA-29b Prevents Cardiac Fibrosis after Myocardial Infarction.

Adv Healthc Mater. 2023-5

[10]
Expression of urinary exosomal miRNA-615-3p and miRNA-3147 in diabetic kidney disease and their association with inflammation and fibrosis.

Ren Fail. 2023-12

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