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Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers

The development of tailored therapies designed to specifically target driver oncogenes has initiated a revolutionary era in cancer biology. The availability of a growing number of selective inhibitors has generated novel experimental and clinical paradigms. These represent an opportunity and a chall...

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Detalles Bibliográficos
Autores principales: Chiarle, Roberto, Ambrogio, Chiara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620112/
https://www.ncbi.nlm.nih.gov/pubmed/37872865
http://dx.doi.org/10.1002/1878-0261.13547
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author Chiarle, Roberto
Ambrogio, Chiara
author_facet Chiarle, Roberto
Ambrogio, Chiara
author_sort Chiarle, Roberto
collection PubMed
description The development of tailored therapies designed to specifically target driver oncogenes has initiated a revolutionary era in cancer biology. The availability of a growing number of selective inhibitors has generated novel experimental and clinical paradigms. These represent an opportunity and a challenge for researchers and clinicians to delve deeper into the intricate dynamics of cancer development and response to treatment. By directly inhibiting key driver oncogenes involved in tumor initiation and progression, scientists have an unprecedented opportunity to conduct longitudinal and clonal evolutionary studies of how cancer cells adapt, rewire, and exploit conflictive or overlapping signaling dependencies in response to treatment in vitro and in vivo. This challenge has to be progressively resolved to discover more effective and personalized cancer therapies.
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spelling pubmed-106201122023-11-03 Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers Chiarle, Roberto Ambrogio, Chiara Mol Oncol Viewpoint The development of tailored therapies designed to specifically target driver oncogenes has initiated a revolutionary era in cancer biology. The availability of a growing number of selective inhibitors has generated novel experimental and clinical paradigms. These represent an opportunity and a challenge for researchers and clinicians to delve deeper into the intricate dynamics of cancer development and response to treatment. By directly inhibiting key driver oncogenes involved in tumor initiation and progression, scientists have an unprecedented opportunity to conduct longitudinal and clonal evolutionary studies of how cancer cells adapt, rewire, and exploit conflictive or overlapping signaling dependencies in response to treatment in vitro and in vivo. This challenge has to be progressively resolved to discover more effective and personalized cancer therapies. John Wiley and Sons Inc. 2023-10-31 /pmc/articles/PMC10620112/ /pubmed/37872865 http://dx.doi.org/10.1002/1878-0261.13547 Text en © 2023 The Authors. Molecular Oncology published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Viewpoint
Chiarle, Roberto
Ambrogio, Chiara
Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
title Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
title_full Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
title_fullStr Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
title_full_unstemmed Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
title_short Exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
title_sort exploiting signaling rewiring in cancer cells with co‐existing oncogenic drivers
topic Viewpoint
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620112/
https://www.ncbi.nlm.nih.gov/pubmed/37872865
http://dx.doi.org/10.1002/1878-0261.13547
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