CRISPR/Cas9 gene editing in gastric cancer: Mechanisms, advances, and therapeutic potential
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.
Authors
- Dimitra Bartzi
- Dimitriοs Schizas (ORCID: https://orcid.org/0000-0002-7046-0112)
- Konstantinos Eleftherios Koumarelas (ORCID: https://orcid.org/0000-0002-5614-4770)
- Grigorios Christodoulidis
- Kyriaki Tsagkidou
- Alexandra Dimaki
- Lydia Lazaridou
- Kalliopi Vakalou
Institutions
- University of Thessaly (GR)
- National and Kapodistrian University of Athens (GR)
- Hellenic Airforce General Hospital (GR)
- University Hospital of Larissa (GR)
- Luzerner Kantonsspital (CH)
- 404 General Military Hospital (GR)
Publication Details
- Journal
- World Journal of Gastrointestinal Pathophysiology
- Published
- 2025-09-19
- DOI
- https://doi.org/10.4291/wjgp.v16.i3.107834
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 0.00