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Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours

Tropomyosin receptor kinase B (TrkB), a transmembrane receptor protein, has been found to play a pivotal role in neural development. This protein is encoded by the neurotrophic receptor tyrosine kinase 2 (NTRK2) gene, and its abnormal activation caused by NTRK2 overexpression or fusion can contribut...

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Autores principales: Li, Yuehua, Wei, Chengjiang, Wang, Wei, Li, Qingfeng, Wang, Zhi‐Chao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896160/
https://www.ncbi.nlm.nih.gov/pubmed/36533776
http://dx.doi.org/10.1002/cjp2.307
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author Li, Yuehua
Wei, Chengjiang
Wang, Wei
Li, Qingfeng
Wang, Zhi‐Chao
author_facet Li, Yuehua
Wei, Chengjiang
Wang, Wei
Li, Qingfeng
Wang, Zhi‐Chao
author_sort Li, Yuehua
collection PubMed
description Tropomyosin receptor kinase B (TrkB), a transmembrane receptor protein, has been found to play a pivotal role in neural development. This protein is encoded by the neurotrophic receptor tyrosine kinase 2 (NTRK2) gene, and its abnormal activation caused by NTRK2 overexpression or fusion can contribute to tumour initiation, progression, and resistance to therapeutics in multiple types of neurogenic tumours. Targeted therapies for this mechanism have been designed and developed in preclinical and clinical studies, including selective TrkB inhibitors and pan‐TRK inhibitors. This review describes the gene structure, biological function, abnormal TrkB activation mechanism, and current‐related targeted therapies in neurogenic tumours.
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spelling pubmed-98961602023-02-08 Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours Li, Yuehua Wei, Chengjiang Wang, Wei Li, Qingfeng Wang, Zhi‐Chao J Pathol Clin Res Review Tropomyosin receptor kinase B (TrkB), a transmembrane receptor protein, has been found to play a pivotal role in neural development. This protein is encoded by the neurotrophic receptor tyrosine kinase 2 (NTRK2) gene, and its abnormal activation caused by NTRK2 overexpression or fusion can contribute to tumour initiation, progression, and resistance to therapeutics in multiple types of neurogenic tumours. Targeted therapies for this mechanism have been designed and developed in preclinical and clinical studies, including selective TrkB inhibitors and pan‐TRK inhibitors. This review describes the gene structure, biological function, abnormal TrkB activation mechanism, and current‐related targeted therapies in neurogenic tumours. John Wiley & Sons, Inc. 2022-12-19 /pmc/articles/PMC9896160/ /pubmed/36533776 http://dx.doi.org/10.1002/cjp2.307 Text en © 2022 The Authors. The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review
Li, Yuehua
Wei, Chengjiang
Wang, Wei
Li, Qingfeng
Wang, Zhi‐Chao
Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours
title Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours
title_full Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours
title_fullStr Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours
title_full_unstemmed Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours
title_short Tropomyosin receptor kinase B (TrkB) signalling: targeted therapy in neurogenic tumours
title_sort tropomyosin receptor kinase b (trkb) signalling: targeted therapy in neurogenic tumours
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896160/
https://www.ncbi.nlm.nih.gov/pubmed/36533776
http://dx.doi.org/10.1002/cjp2.307
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