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Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment
In vivo modeling combined with CRISPR/Cas9-mediated somatic genome editing has contributed to elucidating the functional importance of specific genetic alterations in human tumors. Our recent work uncovered tumor suppressor pathways that affect EGFR-driven lung tumor growth and sensitivity to tyrosi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890383/ https://www.ncbi.nlm.nih.gov/pubmed/35252550 http://dx.doi.org/10.1080/23723556.2021.1994328 |
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author | Foggetti, Giorgia Li, Chuan Cai, Hongchen Petrov, Dmitri A. Winslow, Monte M. Politi, Katerina |
author_facet | Foggetti, Giorgia Li, Chuan Cai, Hongchen Petrov, Dmitri A. Winslow, Monte M. Politi, Katerina |
author_sort | Foggetti, Giorgia |
collection | PubMed |
description | In vivo modeling combined with CRISPR/Cas9-mediated somatic genome editing has contributed to elucidating the functional importance of specific genetic alterations in human tumors. Our recent work uncovered tumor suppressor pathways that affect EGFR-driven lung tumor growth and sensitivity to tyrosine kinase inhibitors and reflect the mutational landscape and treatment outcomes in the human disease. |
format | Online Article Text |
id | pubmed-8890383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-88903832022-03-03 Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment Foggetti, Giorgia Li, Chuan Cai, Hongchen Petrov, Dmitri A. Winslow, Monte M. Politi, Katerina Mol Cell Oncol Author’s Views In vivo modeling combined with CRISPR/Cas9-mediated somatic genome editing has contributed to elucidating the functional importance of specific genetic alterations in human tumors. Our recent work uncovered tumor suppressor pathways that affect EGFR-driven lung tumor growth and sensitivity to tyrosine kinase inhibitors and reflect the mutational landscape and treatment outcomes in the human disease. Taylor & Francis 2022-01-14 /pmc/articles/PMC8890383/ /pubmed/35252550 http://dx.doi.org/10.1080/23723556.2021.1994328 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Author’s Views Foggetti, Giorgia Li, Chuan Cai, Hongchen Petrov, Dmitri A. Winslow, Monte M. Politi, Katerina Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment |
title | Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment |
title_full | Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment |
title_fullStr | Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment |
title_full_unstemmed | Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment |
title_short | Tumor suppressor pathways shape EGFR-driven lung tumor progression and response to treatment |
title_sort | tumor suppressor pathways shape egfr-driven lung tumor progression and response to treatment |
topic | Author’s Views |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8890383/ https://www.ncbi.nlm.nih.gov/pubmed/35252550 http://dx.doi.org/10.1080/23723556.2021.1994328 |
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