The DOI matches its Crossref record; 146 of the 146 references it cites were found in a registry or an index.
Targeting RAF kinases for cancer therapy: BRAF-mutated melanoma and beyond
Open accessAbstract
The identification of mutationally activated BRAF in many cancers altered our conception of the part played by the RAF family of protein kinases in oncogenesis. In this Review, we describe the development of BRAF inhibitors and the results that have emerged from their analysis in both the laboratory and the clinic. We discuss the spectrum of RAF mutations in human cancer and the complex interplay between the tissue of origin and the response to RAF inhibition. Finally, we enumerate mechanisms of resistance to BRAF inhibition that have been characterized and postulate how strategies of RAF pathway inhibition may be extended in scope to benefit not only the thousands of patients who are diagnosed annually with BRAF-mutated metastatic melanoma but also the larger patient population with malignancies harbouring mutationally activated RAF genes that are ineffectively treated with the current generation of BRAF kinase inhibitors.
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Self-citationERK/MAPK signalling pathway and tumorigenesis (Review)
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Metadata
- Authors
- Holderfield, M., Deuker, M. M., McCormick, F., & McMahon, M.
- Venue
- Nature Reviews Cancer
- Published
- 2014-06-24
- Volume
- 14
- Issue
- 7
- Pages
- 455-467
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W1985821753
- Cited by
- 833
- References
- 146
- FWCI
- 5.46
- Type
- journal article
- Language
- en
- Open access
- green
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- Holderfield, M., Deuker, M. M., McCormick, F., & McMahon, M. (2014). Targeting RAF kinases for cancer therapy: BRAF-mutated melanoma and beyond. Nature Reviews Cancer. https://doi.org/10.1038/nrc3760
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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