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Published on: March 15, 2021
Recent advances and applications of CRISPR-Cas9 in cancer immunotherapy
Zaoqu Liu1,2,3, Meixin Shi1, Yuqing Ren4
1Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, Henan, China.
Abstract:
The incidence and mortality of cancer are the major health issue worldwide. Apart from the treatments developed to date, the unsatisfactory therapeutic effects of cancers have not been addressed by broadening the toolbox. The advent of immunotherapy has ushered in a new era in the treatments of solid tumors, but remains limited and requires breaking adverse effects. Meanwhile, the development of advanced technologies can be further boosted by gene analysis and manipulation at the molecular level. The advent of cutting-edge genome editing technology, especially clustered regularly interspaced short palindromic repeats (CRISPR-Cas9), has demonstrated its potential to break the limits of immunotherapy in cancers. In this review, the mechanism of CRISPR-Cas9-mediated genome editing and a powerful CRISPR toolbox are introduced. Furthermore, we focus on reviewing the impact of CRISPR-induced double-strand breaks (DSBs) on cancer immunotherapy (knockout or knockin). Finally, we discuss the CRISPR-Cas9-based genome-wide screening for target identification, emphasis the potential of spatial CRISPR genomics, and present the comprehensive application and challenges in basic research, translational medicine and clinics of CRISPR-Cas9.
Insights
CRISPR-Cas9 gene editing offers a powerful new approach to enhance cancer immunotherapy by overcoming current limitations and improving treatment outcomes. This technology enables precise genetic modifications for better cancer therapies.
Area of Science:
- Oncology
- Genetics
- Immunology
Background:
- Cancer remains a leading global health challenge with limited therapeutic options.
- Immunotherapy has advanced cancer treatment but faces limitations and adverse effects.
- Gene editing technologies, particularly CRISPR-Cas9, present novel strategies for cancer therapy.
Purpose of the Study:
- To review the mechanism and applications of CRISPR-Cas9 in cancer immunotherapy.
- To explore the impact of CRISPR-induced double-strand breaks on immunotherapy efficacy.
- To discuss the role of CRISPR-Cas9 in target identification and future clinical translation.
Main Methods:
- Review of CRISPR-Cas9 genome editing mechanisms.
- Analysis of CRISPR-Cas9 applications in cancer immunotherapy (knockout/knockin).
- Discussion of CRISPR-Cas9-based screening and spatial genomics.
Main Results:
- CRISPR-Cas9 facilitates precise gene manipulation for immunotherapy enhancement.
- CRISPR-induced double-strand breaks can modulate anti-tumor immune responses.
- Genome-wide screening with CRISPR-Cas9 aids in identifying novel therapeutic targets.
Conclusions:
- CRISPR-Cas9 technology holds significant potential to overcome limitations in cancer immunotherapy.
- Further research and clinical translation are crucial for realizing the full impact of CRISPR-Cas9 in oncology.
- This technology promises advancements in basic research, translational medicine, and clinical applications for cancer treatment.
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