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Targeted therapy for head and neck cancer: signaling pathways and clinical studies

Head and neck cancer (HNC) is malignant, genetically complex and difficult to treat and is the sixth most frequent cancer, with tobacco, alcohol and human papillomavirus being major risk factors. Based on epigenetic data, HNC is remarkably heterogeneous, and treatment remains challenging. There is a...

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Autores principales: Li, Qingfang, Tie, Yan, Alu, Aqu, Ma, Xuelei, Shi, Huashan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842704/
https://www.ncbi.nlm.nih.gov/pubmed/36646686
http://dx.doi.org/10.1038/s41392-022-01297-0
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author Li, Qingfang
Tie, Yan
Alu, Aqu
Ma, Xuelei
Shi, Huashan
author_facet Li, Qingfang
Tie, Yan
Alu, Aqu
Ma, Xuelei
Shi, Huashan
author_sort Li, Qingfang
collection PubMed
description Head and neck cancer (HNC) is malignant, genetically complex and difficult to treat and is the sixth most frequent cancer, with tobacco, alcohol and human papillomavirus being major risk factors. Based on epigenetic data, HNC is remarkably heterogeneous, and treatment remains challenging. There is a lack of significant improvement in survival and quality of life in patients with HNC. Over half of HNC patients experience locoregional recurrence or distal metastasis despite the current multiple traditional therapeutic strategies and immunotherapy. In addition, resistance to chemotherapy, radiotherapy and some targeted therapies is common. Therefore, it is urgent to explore more effective and tolerable targeted therapies to improve the clinical outcomes of HNC patients. Recent targeted therapy studies have focused on identifying promising biomarkers and developing more effective targeted therapies. A well understanding of the pathogenesis of HNC contributes to learning more about its inner association, which provides novel insight into the development of small molecule inhibitors. In this review, we summarized the vital signaling pathways and discussed the current potential therapeutic targets against critical molecules in HNC, as well as presenting preclinical animal models and ongoing or completed clinical studies about targeted therapy, which may contribute to a more favorable prognosis of HNC. Targeted therapy in combination with other therapies and its limitations were also discussed.
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spelling pubmed-98427042023-01-18 Targeted therapy for head and neck cancer: signaling pathways and clinical studies Li, Qingfang Tie, Yan Alu, Aqu Ma, Xuelei Shi, Huashan Signal Transduct Target Ther Review Article Head and neck cancer (HNC) is malignant, genetically complex and difficult to treat and is the sixth most frequent cancer, with tobacco, alcohol and human papillomavirus being major risk factors. Based on epigenetic data, HNC is remarkably heterogeneous, and treatment remains challenging. There is a lack of significant improvement in survival and quality of life in patients with HNC. Over half of HNC patients experience locoregional recurrence or distal metastasis despite the current multiple traditional therapeutic strategies and immunotherapy. In addition, resistance to chemotherapy, radiotherapy and some targeted therapies is common. Therefore, it is urgent to explore more effective and tolerable targeted therapies to improve the clinical outcomes of HNC patients. Recent targeted therapy studies have focused on identifying promising biomarkers and developing more effective targeted therapies. A well understanding of the pathogenesis of HNC contributes to learning more about its inner association, which provides novel insight into the development of small molecule inhibitors. In this review, we summarized the vital signaling pathways and discussed the current potential therapeutic targets against critical molecules in HNC, as well as presenting preclinical animal models and ongoing or completed clinical studies about targeted therapy, which may contribute to a more favorable prognosis of HNC. Targeted therapy in combination with other therapies and its limitations were also discussed. Nature Publishing Group UK 2023-01-16 /pmc/articles/PMC9842704/ /pubmed/36646686 http://dx.doi.org/10.1038/s41392-022-01297-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Li, Qingfang
Tie, Yan
Alu, Aqu
Ma, Xuelei
Shi, Huashan
Targeted therapy for head and neck cancer: signaling pathways and clinical studies
title Targeted therapy for head and neck cancer: signaling pathways and clinical studies
title_full Targeted therapy for head and neck cancer: signaling pathways and clinical studies
title_fullStr Targeted therapy for head and neck cancer: signaling pathways and clinical studies
title_full_unstemmed Targeted therapy for head and neck cancer: signaling pathways and clinical studies
title_short Targeted therapy for head and neck cancer: signaling pathways and clinical studies
title_sort targeted therapy for head and neck cancer: signaling pathways and clinical studies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842704/
https://www.ncbi.nlm.nih.gov/pubmed/36646686
http://dx.doi.org/10.1038/s41392-022-01297-0
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