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Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities
Developing drugs that target KRAS, the most frequently mutated oncogene in cancer, has not been successful despite much concerted efforts dedicated towards it in the last thirty years. Considering the key role this driver oncogene plays, the pharmacological drugging of KRAS remains a key challenge f...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850913/ https://www.ncbi.nlm.nih.gov/pubmed/29534749 http://dx.doi.org/10.1186/s13046-018-0719-1 |
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author | Porru, Manuela Pompili, Luca Caruso, Carla Biroccio, Annamaria Leonetti, Carlo |
author_facet | Porru, Manuela Pompili, Luca Caruso, Carla Biroccio, Annamaria Leonetti, Carlo |
author_sort | Porru, Manuela |
collection | PubMed |
description | Developing drugs that target KRAS, the most frequently mutated oncogene in cancer, has not been successful despite much concerted efforts dedicated towards it in the last thirty years. Considering the key role this driver oncogene plays, the pharmacological drugging of KRAS remains a key challenge for cancer research. In this review, we highlight the emerging experimental strategies for blocking KRAS function and signaling and its direct targeting. We also report on the results in this field of research produced by our group. |
format | Online Article Text |
id | pubmed-5850913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58509132018-03-21 Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities Porru, Manuela Pompili, Luca Caruso, Carla Biroccio, Annamaria Leonetti, Carlo J Exp Clin Cancer Res Research Developing drugs that target KRAS, the most frequently mutated oncogene in cancer, has not been successful despite much concerted efforts dedicated towards it in the last thirty years. Considering the key role this driver oncogene plays, the pharmacological drugging of KRAS remains a key challenge for cancer research. In this review, we highlight the emerging experimental strategies for blocking KRAS function and signaling and its direct targeting. We also report on the results in this field of research produced by our group. BioMed Central 2018-03-13 /pmc/articles/PMC5850913/ /pubmed/29534749 http://dx.doi.org/10.1186/s13046-018-0719-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Porru, Manuela Pompili, Luca Caruso, Carla Biroccio, Annamaria Leonetti, Carlo Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities |
title | Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities |
title_full | Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities |
title_fullStr | Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities |
title_full_unstemmed | Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities |
title_short | Targeting KRAS in metastatic colorectal cancer: current strategies and emerging opportunities |
title_sort | targeting kras in metastatic colorectal cancer: current strategies and emerging opportunities |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5850913/ https://www.ncbi.nlm.nih.gov/pubmed/29534749 http://dx.doi.org/10.1186/s13046-018-0719-1 |
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