Natural Biopolymer-Based Delivery of CRISPR/Cas9 for Cancer Treatment

Meng Lin1, Xueyan Wang1

  • 1Department of Pharmacy, West China Hospital, Sichuan University, Chengdu 610041, China.

Pharmaceutics
|January 23, 2024
PubMed

Insights

Natural biopolymers offer a promising solution for delivering CRISPR/Cas9 gene editing tools, enhancing cancer treatment. These materials improve stability and efficiency, overcoming key delivery challenges for clinical applications.

Area of Science:

  • Biomaterials Science
  • Gene Editing Technology
  • Cancer Therapeutics

Background:

  • The clustered, regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) system is a leading gene editing tool for disease treatment, particularly cancer.
  • Efficient delivery of CRISPR/Cas9 (as DNA, mRNA, or ribonucleoprotein) remains a significant hurdle for clinical translation.
  • Nanomaterials are being developed to enhance the stability and delivery efficiency of CRISPR/Cas9 systems.

Purpose of the Study:

  • To review advances in natural biopolymer-based materials for CRISPR/Cas9 delivery in cancer therapy.
  • To highlight the advantages of natural biopolymers, including stability, low toxicity, and biocompatibility.
  • To discuss challenges associated with the clinical translation of these delivery systems.

Main Methods:

  • Literature review focusing on natural biopolymer applications for CRISPR/Cas9 delivery.
  • Analysis of material properties relevant to gene editing delivery (stability, toxicity, biocompatibility).
  • Examination of studies specifically targeting cancer applications.

Main Results:

  • Natural biopolymers demonstrate significant potential as carriers for CRISPR/Cas9 systems.
  • These materials offer improved stability, biocompatibility, and biodegradability compared to other delivery methods.
  • Successful applications in preclinical cancer models have been reported.

Conclusions:

  • Natural biopolymer-based carriers represent a promising strategy for advancing CRISPR/Cas9 gene editing in cancer therapy.
  • Overcoming delivery challenges is crucial for realizing the full clinical potential of CRISPR/Cas9.
  • Further research is needed to address remaining challenges for successful clinical translation.