Related Experiment Video
Updated: May 30, 2025

CRISPR/Cas9 Ribonucleoprotein-mediated Precise Gene Editing by Tube Electroporation
Published on: June 20, 2019
Exosomes-mediated CRISPR/Cas delivery: A cutting-edge frontier in cancer gene therapy
Bhavanisha Rithiga S1, Rajib Dhar1, Arikketh Devi1
1Cancer and Stem Cell Biology Laboratory, Department of Genetic Engineering, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu District, TamilNadu 603203, India.
Abstract:
Cancer is considered the second most common disease globally. In the past few decades, many approaches have been proposed for cancer treatment. One among those is targeted therapy using CRISPR/Cas system which plays a significant role in translational research through gene editing. However, due to its inability to cope with specific targeting, off-target effects, and limited tumor penetration, it is very challenging to use this approach in cancer studies. To increase its efficacy, CRISPR components are engineered into the extracellular vesicles (EVs), especially exosomes (a subpopulation of EVs). Exosomes have a significant role in cellular communication. Exosomes-based CRISPR/Cas system transport for gene editing enhances specificity, reduces off-target effects, and improves the therapeutic potential. This review highlights the role of exosomes and the CRISPR/Cas system in cancer research, exosomes-based CRISPR delivery for cancer treatment, and its future orientation.
Insights
CRISPR/Cas gene editing shows promise for cancer therapy but faces challenges. Engineering CRISPR into exosomes enhances specificity and reduces side effects, improving its potential for treating cancer.
Area of Science:
- Biotechnology
- Genetics
- Oncology
Background:
- Cancer is a leading global disease with ongoing research into novel treatments.
- CRISPR/Cas gene editing offers targeted therapy potential but struggles with specificity and delivery.
- Extracellular vesicles (EVs), particularly exosomes, are key in intercellular communication.
Purpose of the Study:
- To review the application of exosomes and CRISPR/Cas systems in cancer research.
- To explore the use of exosome-mediated CRISPR/Cas delivery for cancer treatment.
- To discuss the future prospects of this therapeutic approach.
Main Methods:
- Review of current literature on CRISPR/Cas systems and exosomes in cancer.
- Analysis of exosome engineering for CRISPR/Cas component encapsulation.
- Evaluation of exosome-based CRISPR/Cas delivery systems for enhanced cancer therapy.
Main Results:
- Exosomes improve CRISPR/Cas system specificity and reduce off-target effects.
- Exosome delivery enhances the therapeutic efficacy of CRISPR/Cas in cancer models.
- Engineered exosomes overcome limitations of direct CRISPR/Cas application.
Conclusions:
- Exosome-mediated CRISPR/Cas delivery represents a promising strategy for advanced cancer treatment.
- This approach enhances gene editing precision and therapeutic outcomes.
- Further research is warranted to optimize exosome-based CRISPR/Cas for clinical application.
Related Concept Videos
CRISPR
Gene Therapy
Homologous Recombination

