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Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma
RTK plays important roles in many cellular signaling processes involved in cancer growth and development. ALK, TRKA, TRKB, TRKC, and ROS1 are RTKs involved in several canonical pathways related to oncogenesis. These proteins can be genetically altered in malignancies, leading to receptor activation...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204873/ https://www.ncbi.nlm.nih.gov/pubmed/30425456 http://dx.doi.org/10.2147/DDDT.S147384 |
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author | Pacenta, Holly L Macy, Margaret E |
author_facet | Pacenta, Holly L Macy, Margaret E |
author_sort | Pacenta, Holly L |
collection | PubMed |
description | RTK plays important roles in many cellular signaling processes involved in cancer growth and development. ALK, TRKA, TRKB, TRKC, and ROS1 are RTKs involved in several canonical pathways related to oncogenesis. These proteins can be genetically altered in malignancies, leading to receptor activation and constitutive signaling through their respective downstream pathways. Neuroblastoma (NB) is the most common extracranial solid tumor in childhood, and despite intensive therapy, there is a high mortality rate in cases with a high-risk disease. Alterations of ALK and differential expression of TRK proteins are reported in a proportion of NB. Several inhibitors of ALK or TRKA/B/C have been evaluated both preclinically and clinically in the treatment of NB. These agents have had variable success and are not routinely used in the treatment of NB. Entrectinib (RXDX-101) is a pan-ALK, TRKA, TRKB, TRKC, and ROS1 inhibitor with activity against tumors with ALK, NTRK1, NTRK2, NTRK3, and ROS1 alterations in Phase I clinical trials in adults. Entrectinib’s activity against both ALK and TRK proteins suggests a possible role in NB treatment, and it is currently under investigation in both pediatric and adult oncology patients. |
format | Online Article Text |
id | pubmed-6204873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62048732018-11-13 Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma Pacenta, Holly L Macy, Margaret E Drug Des Devel Ther Review RTK plays important roles in many cellular signaling processes involved in cancer growth and development. ALK, TRKA, TRKB, TRKC, and ROS1 are RTKs involved in several canonical pathways related to oncogenesis. These proteins can be genetically altered in malignancies, leading to receptor activation and constitutive signaling through their respective downstream pathways. Neuroblastoma (NB) is the most common extracranial solid tumor in childhood, and despite intensive therapy, there is a high mortality rate in cases with a high-risk disease. Alterations of ALK and differential expression of TRK proteins are reported in a proportion of NB. Several inhibitors of ALK or TRKA/B/C have been evaluated both preclinically and clinically in the treatment of NB. These agents have had variable success and are not routinely used in the treatment of NB. Entrectinib (RXDX-101) is a pan-ALK, TRKA, TRKB, TRKC, and ROS1 inhibitor with activity against tumors with ALK, NTRK1, NTRK2, NTRK3, and ROS1 alterations in Phase I clinical trials in adults. Entrectinib’s activity against both ALK and TRK proteins suggests a possible role in NB treatment, and it is currently under investigation in both pediatric and adult oncology patients. Dove Medical Press 2018-10-23 /pmc/articles/PMC6204873/ /pubmed/30425456 http://dx.doi.org/10.2147/DDDT.S147384 Text en © 2018 Pacenta and Macy. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Pacenta, Holly L Macy, Margaret E Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma |
title | Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma |
title_full | Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma |
title_fullStr | Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma |
title_full_unstemmed | Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma |
title_short | Entrectinib and other ALK/TRK inhibitors for the treatment of neuroblastoma |
title_sort | entrectinib and other alk/trk inhibitors for the treatment of neuroblastoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204873/ https://www.ncbi.nlm.nih.gov/pubmed/30425456 http://dx.doi.org/10.2147/DDDT.S147384 |
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