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Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer
Fibroblast growth factor receptor 4 (FGFR4) is a tyrosine kinase receptor that is a member of the fibroblast growth factor receptor family and is stimulated by highly regulated ligand binding. Excessive expression of the receptor and its ligand, especially FGF19, occurs in many types of cancer. Abno...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107720/ https://www.ncbi.nlm.nih.gov/pubmed/33981224 http://dx.doi.org/10.3389/fphar.2021.633453 |
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author | Liu, Yanan Wang, Canwei Li, Jifa Zhu, Jiandong Zhao, Chengguang Xu, Huanhai |
author_facet | Liu, Yanan Wang, Canwei Li, Jifa Zhu, Jiandong Zhao, Chengguang Xu, Huanhai |
author_sort | Liu, Yanan |
collection | PubMed |
description | Fibroblast growth factor receptor 4 (FGFR4) is a tyrosine kinase receptor that is a member of the fibroblast growth factor receptor family and is stimulated by highly regulated ligand binding. Excessive expression of the receptor and its ligand, especially FGF19, occurs in many types of cancer. Abnormal FGFR4 production explains these cancer formations, and therefore, this receptor has emerged as a potential target for inhibiting cancer development. This review discusses the diverse mechanisms of oncogenic activation of FGFR4 and highlights some currently available inhibitors targeting FGFR4. |
format | Online Article Text |
id | pubmed-8107720 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81077202021-05-11 Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer Liu, Yanan Wang, Canwei Li, Jifa Zhu, Jiandong Zhao, Chengguang Xu, Huanhai Front Pharmacol Pharmacology Fibroblast growth factor receptor 4 (FGFR4) is a tyrosine kinase receptor that is a member of the fibroblast growth factor receptor family and is stimulated by highly regulated ligand binding. Excessive expression of the receptor and its ligand, especially FGF19, occurs in many types of cancer. Abnormal FGFR4 production explains these cancer formations, and therefore, this receptor has emerged as a potential target for inhibiting cancer development. This review discusses the diverse mechanisms of oncogenic activation of FGFR4 and highlights some currently available inhibitors targeting FGFR4. Frontiers Media S.A. 2021-04-26 /pmc/articles/PMC8107720/ /pubmed/33981224 http://dx.doi.org/10.3389/fphar.2021.633453 Text en Copyright © 2021 Liu, Wang, Li, Zhu, Zhao and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Liu, Yanan Wang, Canwei Li, Jifa Zhu, Jiandong Zhao, Chengguang Xu, Huanhai Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer |
title | Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer |
title_full | Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer |
title_fullStr | Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer |
title_full_unstemmed | Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer |
title_short | Novel Regulatory Factors and Small-Molecule Inhibitors of FGFR4 in Cancer |
title_sort | novel regulatory factors and small-molecule inhibitors of fgfr4 in cancer |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107720/ https://www.ncbi.nlm.nih.gov/pubmed/33981224 http://dx.doi.org/10.3389/fphar.2021.633453 |
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