This review demonstrates CRISPR/Cas9 enhances chemosensitivity and aids biomarker discovery in colorectal cancer, implying improved therapeutic outcomes.
Colorectal cancer (CRC) remains a significant global health challenge, necessitating advanced molecular therapies to improve outcomes. The CRISPR/Cas9 genome-editing platform has emerged as a transformative tool in CRC research, enabling precise genomic modifications to suppress tumor progression, enhance chemosensitivity, and modulate oncogenic pathways. This review highlights CRISPR/Cas9 applications in CRC models, including MC38 murine and CaCO-2 cell lines, where targeted gene edits demonstrate tumor-suppressive effects. For instance, Par3L protein knockout via CRISPR/Cas9 inhibits proliferation, induces apoptosis, and sensitizes cells to chemotherapy by regulating AMPK signaling. Additionally, AAV-mediated CRISPR editing shows promise in HPV16-driven CRC models. Despite its potential, clinical translation faces challenges such as off-target effects, immunogenicity, and delivery limitations. Advances in engineered CRISPR variants (e.g., xCas9, HypaCas9) and innovative delivery systems are refining specificity and efficacy. CRISPR/Cas9 also accelerates biomarker discovery, paving the way for precision oncology. Overcoming current barriers could revolutionize CRC therapeutics, offering personalized treatment paradigms.
No takes yet. Share an insight, caveat, or question.
Alhasso et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: