Cited by 73Colorectal Cancer Treatments and StudiesProtein Kinase Regulation and GTPase SignalingGenetic factors in colorectal cancer

Precision therapy in RAS mutant colorectal cancer

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Dienstmann, Rodrigo, Connor, Kate, Byrne, Annette T., Fridman, W.H., Lambrechts, D., Sadanandam, A., Trusolino, L., Prehn, J.H.M. +2 more·2020·Gastroenterology

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Crossref · 10.1053/j.gastro.2019.12.051

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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].”

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1 of the 27 references couldn’t be matched to a known paper.

Research works printed but not linked: 4

  1. [4]4. [Roth AD, Tejpar S, Delorenzi M, et al. Prognostic role of KRAS and BRAF in stage II and III resected colon cancer: results of the Translational Study on the PETACC-3,](http://refhub.elsevier.com/S0016-5085(20)30114-1/sref4)
  2. [5]5. [EORTC 40993, SAKK 60-00 Trial. J Clin Oncol 2010;28:466 -474.](http://refhub.elsevier.com/S0016-5085(20)30114-1/sref4)
  3. [9]9. [Ryan MB, Corcoran RB. Therapeutic strategies to target RASmutant cancers. Nat Rev Clin Oncol 2018;15:709 -720.](http://refhub.elsevier.com/S0016-5085(20)30114-1/sref9)
  4. [15]15. [Govindan R, Fakih MG, Price TJ, et al. Phase 1 study of AMG 510, a novel molecule targeting kras g12c mutant solid tumors. Ann Oncol 2019;30(Suppl):v159 -v193.](http://refhub.elsevier.com/S0016-5085(20)30114-1/sref15)

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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)
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
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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