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Receptor Tyrosine Kinase-Targeted Cancer Therapy

In the past two decades, several molecular targeted inhibitors have been developed and evaluated clinically to improve the survival of patients with cancer. Molecular targeted inhibitors inhibit the activities of pathogenic tyrosine kinases. Particularly, aberrant receptor tyrosine kinase (RTK) acti...

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Autores principales: Yamaoka, Toshimitsu, Kusumoto, Sojiro, Ando, Koichi, Ohba, Motoi, Ohmori, Tohru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274851/
https://www.ncbi.nlm.nih.gov/pubmed/30404198
http://dx.doi.org/10.3390/ijms19113491
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author Yamaoka, Toshimitsu
Kusumoto, Sojiro
Ando, Koichi
Ohba, Motoi
Ohmori, Tohru
author_facet Yamaoka, Toshimitsu
Kusumoto, Sojiro
Ando, Koichi
Ohba, Motoi
Ohmori, Tohru
author_sort Yamaoka, Toshimitsu
collection PubMed
description In the past two decades, several molecular targeted inhibitors have been developed and evaluated clinically to improve the survival of patients with cancer. Molecular targeted inhibitors inhibit the activities of pathogenic tyrosine kinases. Particularly, aberrant receptor tyrosine kinase (RTK) activation is a potential therapeutic target. An increased understanding of genetics, cellular biology and structural biology has led to the development of numerous important therapeutics. Pathogenic RTK mutations, deletions, translocations and amplification/over-expressions have been identified and are currently being examined for their roles in cancers. Therapies targeting RTKs are categorized as small-molecule inhibitors and monoclonal antibodies. Studies are underway to explore abnormalities in 20 types of RTK subfamilies in patients with cancer or other diseases. In this review, we describe representative RTKs important for developing cancer therapeutics and predicting or evaluated resistance mechanisms.
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spelling pubmed-62748512018-12-15 Receptor Tyrosine Kinase-Targeted Cancer Therapy Yamaoka, Toshimitsu Kusumoto, Sojiro Ando, Koichi Ohba, Motoi Ohmori, Tohru Int J Mol Sci Review In the past two decades, several molecular targeted inhibitors have been developed and evaluated clinically to improve the survival of patients with cancer. Molecular targeted inhibitors inhibit the activities of pathogenic tyrosine kinases. Particularly, aberrant receptor tyrosine kinase (RTK) activation is a potential therapeutic target. An increased understanding of genetics, cellular biology and structural biology has led to the development of numerous important therapeutics. Pathogenic RTK mutations, deletions, translocations and amplification/over-expressions have been identified and are currently being examined for their roles in cancers. Therapies targeting RTKs are categorized as small-molecule inhibitors and monoclonal antibodies. Studies are underway to explore abnormalities in 20 types of RTK subfamilies in patients with cancer or other diseases. In this review, we describe representative RTKs important for developing cancer therapeutics and predicting or evaluated resistance mechanisms. MDPI 2018-11-06 /pmc/articles/PMC6274851/ /pubmed/30404198 http://dx.doi.org/10.3390/ijms19113491 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yamaoka, Toshimitsu
Kusumoto, Sojiro
Ando, Koichi
Ohba, Motoi
Ohmori, Tohru
Receptor Tyrosine Kinase-Targeted Cancer Therapy
title Receptor Tyrosine Kinase-Targeted Cancer Therapy
title_full Receptor Tyrosine Kinase-Targeted Cancer Therapy
title_fullStr Receptor Tyrosine Kinase-Targeted Cancer Therapy
title_full_unstemmed Receptor Tyrosine Kinase-Targeted Cancer Therapy
title_short Receptor Tyrosine Kinase-Targeted Cancer Therapy
title_sort receptor tyrosine kinase-targeted cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274851/
https://www.ncbi.nlm.nih.gov/pubmed/30404198
http://dx.doi.org/10.3390/ijms19113491
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