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Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit

Head and neck squamous cell carcinomas (HNSCC) are common human malignancies with poor clinical outcomes. The 5-year survival rates for patients with advanced stage HNSCC have not changed appreciably in the past few decades, underscoring a dire need for improved therapeutic options. Recent studies h...

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Detalles Bibliográficos
Autor principal: Johnson, Daniel E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sun Yat-sen University Cancer Center 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607312/
https://www.ncbi.nlm.nih.gov/pubmed/22257382
http://dx.doi.org/10.5732/cjc.011.10404
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author Johnson, Daniel E.
author_facet Johnson, Daniel E.
author_sort Johnson, Daniel E.
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description Head and neck squamous cell carcinomas (HNSCC) are common human malignancies with poor clinical outcomes. The 5-year survival rates for patients with advanced stage HNSCC have not changed appreciably in the past few decades, underscoring a dire need for improved therapeutic options. Recent studies have elucidated a key signaling axis, the EGFR-STAT3-Bcl-X(L) signaling axis, that is aberrantly activated in a majority of HNSCC and contributes to the proliferation and survival of malignant cells. Considerable effort is being placed on developing highly specific inhibitors of different components of this pathway. This review highlights the progress that is being made towards achieving potent inhibition of the EGFR-STAT3-Bcl-X(L) signaling axis in HNSCC and the promising therapeutic strategies that are currently under development for this disease.
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spelling pubmed-36073122013-07-01 Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit Johnson, Daniel E. Chin J Cancer Review Head and neck squamous cell carcinomas (HNSCC) are common human malignancies with poor clinical outcomes. The 5-year survival rates for patients with advanced stage HNSCC have not changed appreciably in the past few decades, underscoring a dire need for improved therapeutic options. Recent studies have elucidated a key signaling axis, the EGFR-STAT3-Bcl-X(L) signaling axis, that is aberrantly activated in a majority of HNSCC and contributes to the proliferation and survival of malignant cells. Considerable effort is being placed on developing highly specific inhibitors of different components of this pathway. This review highlights the progress that is being made towards achieving potent inhibition of the EGFR-STAT3-Bcl-X(L) signaling axis in HNSCC and the promising therapeutic strategies that are currently under development for this disease. Sun Yat-sen University Cancer Center 2012-07 /pmc/articles/PMC3607312/ /pubmed/22257382 http://dx.doi.org/10.5732/cjc.011.10404 Text en Chinese Journal of Cancer http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Review
Johnson, Daniel E.
Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
title Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
title_full Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
title_fullStr Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
title_full_unstemmed Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
title_short Targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
title_sort targeting proliferation and survival pathways in head and neck cancer for therapeutic benefit
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3607312/
https://www.ncbi.nlm.nih.gov/pubmed/22257382
http://dx.doi.org/10.5732/cjc.011.10404
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