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RAS-mediated tumor stress adaptation and the targeting opportunities it presents
Cellular stress is known to function in synergistic cooperation with oncogenic mutations during tumorigenesis to drive cancer progression. Oncogenic RAS is a strong inducer of a variety of pro-tumorigenic cellular stresses, and also enhances the ability of cells to tolerate these stresses through mu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844456/ https://www.ncbi.nlm.nih.gov/pubmed/35147163 http://dx.doi.org/10.1242/dmm.049280 |
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author | Redding, Alexandra Aplin, Andrew E. Grabocka, Elda |
author_facet | Redding, Alexandra Aplin, Andrew E. Grabocka, Elda |
author_sort | Redding, Alexandra |
collection | PubMed |
description | Cellular stress is known to function in synergistic cooperation with oncogenic mutations during tumorigenesis to drive cancer progression. Oncogenic RAS is a strong inducer of a variety of pro-tumorigenic cellular stresses, and also enhances the ability of cells to tolerate these stresses through multiple mechanisms. Many of these oncogenic, RAS-driven, stress-adaptive mechanisms have also been implicated in tolerance and resistance to chemotherapy and to therapies that target the RAS pathway. Understanding how oncogenic RAS shapes cellular stress adaptation and how this functions in drug resistance is of vital importance for identifying new therapeutic targets and therapeutic combinations to treat RAS-driven cancers. |
format | Online Article Text |
id | pubmed-8844456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88444562022-02-15 RAS-mediated tumor stress adaptation and the targeting opportunities it presents Redding, Alexandra Aplin, Andrew E. Grabocka, Elda Dis Model Mech Review Cellular stress is known to function in synergistic cooperation with oncogenic mutations during tumorigenesis to drive cancer progression. Oncogenic RAS is a strong inducer of a variety of pro-tumorigenic cellular stresses, and also enhances the ability of cells to tolerate these stresses through multiple mechanisms. Many of these oncogenic, RAS-driven, stress-adaptive mechanisms have also been implicated in tolerance and resistance to chemotherapy and to therapies that target the RAS pathway. Understanding how oncogenic RAS shapes cellular stress adaptation and how this functions in drug resistance is of vital importance for identifying new therapeutic targets and therapeutic combinations to treat RAS-driven cancers. The Company of Biologists Ltd 2022-02-11 /pmc/articles/PMC8844456/ /pubmed/35147163 http://dx.doi.org/10.1242/dmm.049280 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Review Redding, Alexandra Aplin, Andrew E. Grabocka, Elda RAS-mediated tumor stress adaptation and the targeting opportunities it presents |
title | RAS-mediated tumor stress adaptation and the targeting opportunities it presents |
title_full | RAS-mediated tumor stress adaptation and the targeting opportunities it presents |
title_fullStr | RAS-mediated tumor stress adaptation and the targeting opportunities it presents |
title_full_unstemmed | RAS-mediated tumor stress adaptation and the targeting opportunities it presents |
title_short | RAS-mediated tumor stress adaptation and the targeting opportunities it presents |
title_sort | ras-mediated tumor stress adaptation and the targeting opportunities it presents |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844456/ https://www.ncbi.nlm.nih.gov/pubmed/35147163 http://dx.doi.org/10.1242/dmm.049280 |
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