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The Frequency of Ras Mutations in Cancer

Overview
Journal Cancer Res
Specialty Oncology
Date 2020 Mar 27
PMID 32209560
Citations 432
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Abstract

Ras is frequently mutated in cancer, however, there is a lack of consensus in the literature regarding the cancer mutation frequency of Ras, with quoted values varying from 10%-30%. This variability is at least in part due to the selective aggregation of data from different databases and the dominant influence of particular cancer types and particular Ras isoforms within these datasets. To provide a more definitive figure for Ras mutation frequency in cancer, we cross-referenced the data in all major publicly accessible cancer mutation databases to determine reliable mutation frequency values for each Ras isoform in all major cancer types. These percentages were then applied to current U.S. cancer incidence statistics to estimate the number of new patients each year that have Ras-mutant cancers. We find that approximately 19% of patients with cancer harbor Ras mutations, equivalent to approximately 3.4 million new cases per year worldwide. We discuss the Ras isoform and mutation-specific trends evident within the datasets that are relevant to current Ras-targeted therapies.

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References
1.
Brandt R, Sell T, Luthen M, Uhlitz F, Klinger B, Riemer P . Cell type-dependent differential activation of ERK by oncogenic KRAS in colon cancer and intestinal epithelium. Nat Commun. 2019; 10(1):2919. PMC: 6606648. DOI: 10.1038/s41467-019-10954-y. View

2.
Tate J, Bamford S, Jubb H, Sondka Z, Beare D, Bindal N . COSMIC: the Catalogue Of Somatic Mutations In Cancer. Nucleic Acids Res. 2018; 47(D1):D941-D947. PMC: 6323903. DOI: 10.1093/nar/gky1015. View

3.
Suh J, Johnson A, Albacker L, Wang K, Chmielecki J, Frampton G . Comprehensive Genomic Profiling Facilitates Implementation of the National Comprehensive Cancer Network Guidelines for Lung Cancer Biomarker Testing and Identifies Patients Who May Benefit From Enrollment in Mechanism-Driven Clinical Trials. Oncologist. 2016; 21(6):684-91. PMC: 4912374. DOI: 10.1634/theoncologist.2016-0030. View

4.
Xiong Y, Lu J, Hunter J, Li L, Scott D, Choi H . Covalent Guanosine Mimetic Inhibitors of G12C KRAS. ACS Med Chem Lett. 2017; 8(1):61-66. PMC: 5238463. DOI: 10.1021/acsmedchemlett.6b00373. View

5.
Burd C, Liu W, Huynh M, Waqas M, Gillahan J, Clark K . Mutation-specific RAS oncogenicity explains NRAS codon 61 selection in melanoma. Cancer Discov. 2014; 4(12):1418-29. PMC: 4258185. DOI: 10.1158/2159-8290.CD-14-0729. View