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Published on: May 23, 2025
The Potential Revolution of Cancer Treatment with CRISPR Technology
Dimitrios Stefanoudakis1, Nikhita Kathuria-Prakash2, Alexander W Sun3
1School of Medicine, National & Kapodistrian University of Athens, 15772 Athens, Greece.
Abstract:
Immuno-oncology (IO) and targeted therapies, such as small molecule inhibitors, have changed the landscape of cancer treatment and prognosis; however, durable responses have been difficult to achieve due to tumor heterogeneity, development of drug resistance, and adverse effects that limit dosing and prolonged drug use. To improve upon the current medicinal armamentarium, there is an urgent need for new ways to understand, reverse, and treat carcinogenesis. Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein (Cas) 9 is a powerful and efficient tool for genome editing that has shown significant promise for developing new therapeutics. While CRISPR/Cas9 has been successfully used for pre-clinical cancer research, its use in the clinical setting is still in an early stage of development. The purpose of this review is to describe the CRISPR technology and to provide an overview of its current applications and future potential as cancer therapies.
Insights
Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein (Cas) 9 gene editing offers new cancer therapy potential. This review explores CRISPR/Cas9 technology, its applications, and future promise in treating cancer.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Immuno-oncology and targeted therapies have advanced cancer treatment but face challenges like tumor heterogeneity and drug resistance.
- Durable responses remain difficult to achieve, necessitating novel therapeutic strategies.
- There is a critical need for innovative approaches to understand, reverse, and treat carcinogenesis.
Purpose of the Study:
- To review the Clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein (Cas) 9 technology.
- To provide an overview of current applications of CRISPR/Cas9 in cancer research.
- To discuss the future potential of CRISPR/Cas9 as a cancer therapeutic.
Main Methods:
- Review of existing literature on CRISPR/Cas9 technology and its applications in cancer.
- Analysis of pre-clinical research findings using CRISPR/Cas9 for cancer therapy development.
- Exploration of the challenges and future directions for clinical translation.
Main Results:
- CRISPR/Cas9 is a powerful and efficient genome editing tool with significant therapeutic promise.
- CRISPR/Cas9 has been successfully utilized in pre-clinical cancer research.
- Clinical application of CRISPR/Cas9 for cancer treatment is still in early developmental stages.
Conclusions:
- CRISPR/Cas9 technology holds substantial promise for developing novel cancer therapies.
- Further research and clinical development are required to fully realize the potential of CRISPR/Cas9 in oncology.
- Overcoming challenges in clinical translation is crucial for implementing CRISPR/Cas9-based cancer treatments.
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