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Updated: May 10, 2026

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
Next-generation gene editing strategies in cancer: Integrating CRISPR, PROTACs, and advanced molecular technologies
Akash Vikal1, Rashmi Maurya2, Pradeep Kumar3
1Sahu Onkar Saran School of Pharmacy, Faculty of Pharmacy, IFTM University, Moradabad, India.
Abstract:
Cancer is a significant therapeutic problem as tumors are heterogeneous, multidrug-resistant, and oncogenic drivers are undruggable. Genome editing and targeted protein degradation are emerging approaches that are transforming precision oncology by allowing genetic and proteomic interventions. Such technologies as CRISPR-based systems and proteolysis-targeting chimeras (PROTACs) are alternative methods of correcting genes and the selective removal of a protein. Their combination provides them with new possibilities regarding long-lasting and specific cancer treatment and discovery of new therapeutic targets. Although this has good news, there are delivery, off-target effects and safety challenges. The continued advancements in nanotechnology, artificial intelligence (AI), and personalized medicine will be likely to improve clinical translation. Generally, the integration of these technologies is an inducing trend in the treatment of cancer in the next generation.
Insights
Genome editing and targeted protein degradation, including CRISPR and PROTACs, offer new cancer treatment strategies by correcting genes and removing proteins. Challenges remain, but nanotechnology, AI, and personalized medicine promise improved clinical translation.
Area of Science:
- Oncology
- Biotechnology
- Genetics
Background:
- Cancer presents significant therapeutic challenges due to tumor heterogeneity, multidrug resistance, and undruggable oncogenic drivers.
- Precision oncology requires innovative approaches for genetic and proteomic interventions.
Purpose of the Study:
- To explore the transformative potential of genome editing and targeted protein degradation in cancer therapy.
- To highlight the synergistic possibilities of combining CRISPR-based systems and proteolysis-targeting chimeras (PROTACs).
Main Methods:
- Utilizing CRISPR-based systems for gene correction.
- Employing proteolysis-targeting chimeras (PROTACs) for selective protein removal.
- Investigating the combined application of these technologies for cancer treatment.
Main Results:
- The combination of genome editing and targeted protein degradation offers novel possibilities for long-lasting and specific cancer treatment.
- These approaches facilitate the discovery of new therapeutic targets.
- Delivery, off-target effects, and safety are identified challenges.
Conclusions:
- Advancements in nanotechnology, artificial intelligence (AI), and personalized medicine are expected to enhance clinical translation.
- The integration of these cutting-edge technologies represents a significant trend in next-generation cancer treatment.
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