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Updated: Jan 16, 2026

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
Published on: May 25, 2018
CRISPR/Cas9 gene editing in gastric cancer: Mechanisms, advances, and therapeutic potential
Grigorios Christodoulidis1, Dimitra Bartzi2, Kyriaki Tsagkidou3
1Department of General Surgery, University Hospital of Larissa, Larissa 41110, Thessalia, Greece. gregsurg@yahoo.gr.
Abstract:
Gastric cancer (GC) remains one of the leading causes of cancer-related mortality worldwide, necessitating innovative approaches for its diagnosis and treatment. Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9), a revolutionary gene-editing technology, has emerged as a powerful tool for unraveling the molecular mechanisms underlying GC and for advancing precision medicine strategies. This review explores the current applications of CRISPR/Cas9 in GC research, including the identification of oncogenes and tumor suppressors, modeling tumor microenvironment interactions, and developing gene-based therapies. We highlight recent breakthroughs in genome editing that have enhanced our understanding of GC pathogenesis and resistance mechanisms to conventional therapies. Additionally, we discuss the potential of CRISPR/Cas9 for therapeutic gene editing in GC, addressing challenges such as off-target effects, delivery methods, and ethical considerations. By summarizing the progress and limitations of CRISPR/Cas9 in GC, this review aims to provide a comprehensive perspective on how this transformative technology could shape future strategies for the prevention, diagnosis, and treatment of GC.
Insights
Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) gene editing offers new ways to study gastric cancer (GC) and develop precision treatments. This technology aids in understanding GC
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Gastric cancer (GC) is a major global health concern, driving the need for advanced diagnostic and therapeutic strategies.
- Gene-editing technologies like CRISPR/Cas9 present novel opportunities for understanding GC's molecular underpinnings.
Purpose of the Study:
- To review the current applications of CRISPR/Cas9 technology in gastric cancer research.
- To explore the potential of CRISPR/Cas9 for developing novel gene-based therapies for GC.
- To discuss the challenges and future directions of CRISPR/Cas9 in GC management.
Main Methods:
- Review of current literature on CRISPR/Cas9 applications in gastric cancer research.
- Analysis of CRISPR/Cas9's role in identifying oncogenes, tumor suppressors, and modeling tumor microenvironment.
- Evaluation of gene editing advancements for understanding GC pathogenesis and therapeutic resistance.
Main Results:
- CRISPR/Cas9 has been instrumental in identifying key molecular players in GC development and progression.
- Genome editing has deepened the understanding of GC resistance mechanisms to existing therapies.
- CRISPR/Cas9 shows promise for developing targeted gene therapies for gastric cancer.
Conclusions:
- CRISPR/Cas9 technology is a powerful tool for advancing gastric cancer research and precision medicine.
- Addressing challenges like off-target effects, delivery, and ethical considerations is crucial for clinical translation.
- This technology holds significant potential to revolutionize the prevention, diagnosis, and treatment of gastric cancer.
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