Nanomedicine for Gene Delivery and Drug Repurposing in the Treatment of Muscular Dystrophies.
Ilaria AndreanaMathieu RepellinFlavia CartonDavid KryzaStéphanie BriançonBénédicte ChazaudRémi MounierSilvia ArpiccoManuela MalatestaBarbara StellaGiovanna LolloPublished in: Pharmaceutics (2021)
Muscular Dystrophies (MDs) are a group of rare inherited genetic muscular pathologies encompassing a variety of clinical phenotypes, gene mutations and mechanisms of disease. MDs undergo progressive skeletal muscle degeneration causing severe health problems that lead to poor life quality, disability and premature death. There are no available therapies to counteract the causes of these diseases and conventional treatments are administered only to mitigate symptoms. Recent understanding on the pathogenetic mechanisms allowed the development of novel therapeutic strategies based on gene therapy, genome editing CRISPR/Cas9 and drug repurposing approaches. Despite the therapeutic potential of these treatments, once the actives are administered, their instability, susceptibility to degradation and toxicity limit their applications. In this frame, the design of delivery strategies based on nanomedicines holds great promise for MD treatments. This review focuses on nanomedicine approaches able to encapsulate therapeutic agents such as small chemical molecules and oligonucleotides to target the most common MDs such as Duchenne Muscular Dystrophy and the Myotonic Dystrophies. The challenge related to in vitro and in vivo testing of nanosystems in appropriate animal models is also addressed. Finally, the most promising nanomedicine-based strategies are highlighted and a critical view in future developments of nanomedicine for neuromuscular diseases is provided.
Keyphrases
- crispr cas
- genome editing
- duchenne muscular dystrophy
- gene therapy
- cancer therapy
- skeletal muscle
- resistance training
- multiple sclerosis
- mental health
- healthcare
- public health
- oxidative stress
- drug induced
- risk assessment
- adverse drug
- genome wide
- body composition
- early onset
- quality improvement
- gene expression
- copy number
- adipose tissue
- climate change
- human health
- social media
- nucleic acid