| Literature DB >> 33712155 |
Milad Ashrafizadeh1, Masoud Delfi2, Farid Hashemi3, Amirhossein Zabolian4, Hossein Saleki4, Morteza Bagherian4, Negar Azami4, Mahdi Vasheghani Farahani4, Seyed Omid Sharifzadeh4, Soodeh Hamzehlou4, Kiavash Hushmandi5, Pooyan Makvandi6, Ali Zarrabi7, Michael R Hamblin8, Rajender S Varma9.
Abstract
Gene therapy is an emerging and promising strategy in cancer therapy where small interfering RNA (siRNA) system has been deployed for down-regulation of targeted gene and subsequent inhibition in cancer progression; some issues with siRNA, however, linger namely, its off-targeting property and degradation by enzymes. Nanoparticles can be applied for the encapsulation of siRNA thus enhancing its efficacy in gene silencing where chitosan (CS), a linear alkaline polysaccharide derived from chitin, with superb properties such as biodegradability, biocompatibility, stability and solubility, can play a vital role. Herein, the potential of CS nanoparticles has been discussed for the delivery of siRNA in cancer therapy; proliferation, metastasis and chemoresistance are suppressed by siRNA-loaded CS nanoparticles, especially the usage of pH-sensitive CS nanoparticles. CS nanoparticles can provide a platform for the co-delivery of siRNA and anti-tumor agents with their enhanced stability via chemical modifications. As pre-clinical experiments are in agreement with potential of CS-based nanoparticles for siRNA delivery, and these carriers possess biocompatibiliy and are safe, further studies can focus on evaluating their utilization in cancer patients.Entities:
Keywords: Cancer therapy; Chitosan; Gene delivery; Nanoparticle; Small interfering RNA (siRNA)
Mesh:
Substances:
Year: 2021 PMID: 33712155 DOI: 10.1016/j.carbpol.2021.117809
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381