MicroRNA-targeting nanomedicines for the treatment of intervertebral disc degeneration

被引:3
|
作者
Genedy, Hussein H. [1 ,2 ]
Humbert, Paul [1 ]
Laoulaou, Bilel [1 ,2 ]
Le Moal, Brian [1 ,2 ]
Fusellier, Marion [1 ,3 ]
Passirani, Catherine [2 ]
Le Visage, Catherine [1 ]
Guicheux, Jerome [1 ]
Lepeltier, Elise [2 ,4 ]
Clouet, Johann [1 ]
机构
[1] Nantes Univ, Oniris, CHU Nantes, INSERM,Regenerat Med & Skeleton RMeS,UMR 1229, Nantes, France
[2] Univ Angers, SFR ICAT, MINT, CNRS,INSERM, F-49000 Angers, France
[3] Coll Vet Med Food Sci & Engn, Dept Diagnost Imaging, CRIP, ONIRIS, F-44307 Nantes, France
[4] Inst Univ France IUF, Paris, France
关键词
Intervertebral disc degeneration (IVDD); Nucleus pulposus cells (NP cells); microRNA (miR); Nanomedicine; NUCLEUS PULPOSUS CELLS; SOLID LIPID NANOPARTICLES; LOW-BACK-PAIN; DRUG-DELIVERY; IN-VITRO; MACROMOLECULAR THERAPEUTICS; INFLAMMATORY RESPONSE; EXTRACELLULAR-MATRIX; CANCER-TREATMENT; NONCODING RNAS;
D O I
10.1016/j.addr.2024.115214
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Low back pain stands as a pervasive global health concern, afflicting almost 80% of adults at some point in their lives with nearly 40% attributable to intervertebral disc degeneration (IVDD). As only symptomatic relief can be offered to patients there is a dire need for innovative treatments. Given the accumulating evidence that multiple microRNAs (miRs) are dysregulated during IVDD, they could have a huge potential against this debilitating condition. The way mills can profoundly modulate signaling pathways and influence several cellular processes at once is particularly exciting to tackle this multifaceted disorder. However, mill delivery encounters extracellular and intracellular biological barriers. A promising technology to address this challenge is the vectorization of mills within nanoparticles, providing both protection and enhancing their uptake within the scarce target cells of the degenerated IVD. This comprehensive review presents the diverse spectrum of mills' connection with IVDD and demonstrates their therapeutic potential when vectorized in nanomedicines.
引用
收藏
页数:23
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