Precision therapy in RAS mutant colorectal cancer
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In RAS-mutant CRC, CRISPR has been increasingly employed in preclinical models to interrogate pathway dependencies, identify synthetic lethal interactions, and understand resistance mechanisms to targeted therapies.
“In RAS-mutant CRC, CRISPR has been increasingly employed in preclinical models to interrogate pathway dependencies, identify synthetic lethal interactions, and understand resistance mechanisms to targeted therapies [102].”
From RAS Mutations in Advanced Colorectal Cancer: Mechanisms, Clinical Implications, and Novel Therapeutic Approaches (2025) · cites this paper as [102]
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- Authors
- Dienstmann, R., Connor, K., Byrne, A. T., Fridman, W. H., Lambrechts, D., Sadanandam, A., Trusolino, L., Prehn, J. H. M., Tabernero, J., & Kolch, W.
- Affiliations
- Vall d'Hebron Institute of Oncology (ES)
- Royal College of Surgeons in Ireland (IE)
- ORCID
- Venue
- Gastroenterology
- Publisher
- Elsevier BV
- Published
- 2020-03
- Volume
- 158
- Issue
- 4
- Pages
- 806-811
- ISSN
- 0016-5085 (ISSN-L)
- OpenAlex
- W2999396499
- Cited by
- 73
- References
- 27
- Citations by year
- 2026: 8 · 2025: 15 · 2024: 21 · 2023: 14 · 2022: 5 · 2021: 5 · 2020: 5
- FWCI
- 2.63
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Gastroenterology (publishedVersion)
- PubMed (publishedVersion)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, cc-by)
- Figshare (submittedVersion, cc-by-nc-sa)
- Lirias (submittedVersion)
- Funders
- Science Foundation Ireland (13/CDA/2183, 14/IA/2395, 14/IA/2582)
- Horizon 2020 (754923)
- Topics
- Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Health Sciences › Medicine › Pathology and Forensic Medicine › Genetic factors in colorectal cancer
- Keywords
- RAS mutations, colorectal cancer, KRAS, NRAS, HRAS, precision therapy, oncogenic signaling, targeted therapy
- MeSH terms
- Gain of Function Mutation, Antineoplastic Combined Chemotherapy Protocols, Clinical Trials as Topic, Humans, Membrane Proteins, Colorectal Neoplasms, Proto-Oncogene Proteins p21(ras), Treatment Outcome, Drug Resistance, Neoplasm, Mutation, Missense, GTP Phosphohydrolases, MAP Kinase Signaling System, Protein Kinase Inhibitors, Microsatellite Instability, Precision Medicine
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