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Direct Ras G12C inhibitors: crossing the rubicon
Despite its status as the most commonly mutated oncogene in cancer, Ras has long been considered ‘undruggable’. In 2019, we will see the first clinical trial results for direct mutant Ras inhibitors, a result of persistent cross-disciplinary research that has been informed by a number of previous cl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6738074/ https://www.ncbi.nlm.nih.gov/pubmed/31239544 http://dx.doi.org/10.1038/s41416-019-0499-1 |
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author | Lindsay, Colin R. Blackhall, Fiona H. |
author_facet | Lindsay, Colin R. Blackhall, Fiona H. |
author_sort | Lindsay, Colin R. |
collection | PubMed |
description | Despite its status as the most commonly mutated oncogene in cancer, Ras has long been considered ‘undruggable’. In 2019, we will see the first clinical trial results for direct mutant Ras inhibitors, a result of persistent cross-disciplinary research that has been informed by a number of previous clinical and biological failures. |
format | Online Article Text |
id | pubmed-6738074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67380742019-09-12 Direct Ras G12C inhibitors: crossing the rubicon Lindsay, Colin R. Blackhall, Fiona H. Br J Cancer Editorial Despite its status as the most commonly mutated oncogene in cancer, Ras has long been considered ‘undruggable’. In 2019, we will see the first clinical trial results for direct mutant Ras inhibitors, a result of persistent cross-disciplinary research that has been informed by a number of previous clinical and biological failures. Nature Publishing Group UK 2019-06-26 2019-07-30 /pmc/articles/PMC6738074/ /pubmed/31239544 http://dx.doi.org/10.1038/s41416-019-0499-1 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Editorial Lindsay, Colin R. Blackhall, Fiona H. Direct Ras G12C inhibitors: crossing the rubicon |
title | Direct Ras G12C inhibitors: crossing the rubicon |
title_full | Direct Ras G12C inhibitors: crossing the rubicon |
title_fullStr | Direct Ras G12C inhibitors: crossing the rubicon |
title_full_unstemmed | Direct Ras G12C inhibitors: crossing the rubicon |
title_short | Direct Ras G12C inhibitors: crossing the rubicon |
title_sort | direct ras g12c inhibitors: crossing the rubicon |
topic | Editorial |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6738074/ https://www.ncbi.nlm.nih.gov/pubmed/31239544 http://dx.doi.org/10.1038/s41416-019-0499-1 |
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