Cargando…

Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020

Since the discovery of anaplastic lymphoma kinase fusion-positive (ALK+) NSCLC in 2007, the methods to detect ALK+ NSCLC have evolved and expanded from fluorescence in situ hybridization and immunohistochemistry to next-generation DNA sequencing, targeted RNA sequencing, and whole transcriptome sequ...

Descripción completa

Detalles Bibliográficos
Autores principales: Ou, Sai-Hong Ignatius, Zhu, Viola W., Nagasaka, Misako
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474466/
https://www.ncbi.nlm.nih.gov/pubmed/34589917
http://dx.doi.org/10.1016/j.jtocrr.2020.100015
_version_ 1784575230323195904
author Ou, Sai-Hong Ignatius
Zhu, Viola W.
Nagasaka, Misako
author_facet Ou, Sai-Hong Ignatius
Zhu, Viola W.
Nagasaka, Misako
author_sort Ou, Sai-Hong Ignatius
collection PubMed
description Since the discovery of anaplastic lymphoma kinase fusion-positive (ALK+) NSCLC in 2007, the methods to detect ALK+ NSCLC have evolved and expanded from fluorescence in situ hybridization and immunohistochemistry to next-generation DNA sequencing, targeted RNA sequencing, and whole transcriptome sequencing. As such, the deep sequencing methods have resulted in the expansion of distinct fusion partners identified in ALK+ NSCLC to 90 (one variant PLEKHM2-ALK is found in small cell lung cancer but included in this catalog) by the end of January 2020; about 65 of them (since 2018) and most of the recent novel fusion partners were reported from China. Thirty-four of the distinct fusion partners are located on the short arm of chromosome 2; 28 of these 34 fusion partners are located on 2p21-25, in which ALK is located on 2p23.2-p23.1. Many of these new ALK+ NSCLC fusion variants have responded to ALK tyrosine kinase inhibitors (TKIs). Several of these novel ALK fusion variants were identified as being resistant to EGFR TKIs or as dual 3’ALK fusions. In addition, at least 28 intergenic ALK rearrangements have also been reported, with three of them reported as responding to crizotinib. This review aims to serve as a central source of reference of fusion partners in ALK+ NSCLC for clinicians and scientists. We aim to update and improve the list going forward.
format Online
Article
Text
id pubmed-8474466
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-84744662021-09-28 Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020 Ou, Sai-Hong Ignatius Zhu, Viola W. Nagasaka, Misako JTO Clin Res Rep Review Article Since the discovery of anaplastic lymphoma kinase fusion-positive (ALK+) NSCLC in 2007, the methods to detect ALK+ NSCLC have evolved and expanded from fluorescence in situ hybridization and immunohistochemistry to next-generation DNA sequencing, targeted RNA sequencing, and whole transcriptome sequencing. As such, the deep sequencing methods have resulted in the expansion of distinct fusion partners identified in ALK+ NSCLC to 90 (one variant PLEKHM2-ALK is found in small cell lung cancer but included in this catalog) by the end of January 2020; about 65 of them (since 2018) and most of the recent novel fusion partners were reported from China. Thirty-four of the distinct fusion partners are located on the short arm of chromosome 2; 28 of these 34 fusion partners are located on 2p21-25, in which ALK is located on 2p23.2-p23.1. Many of these new ALK+ NSCLC fusion variants have responded to ALK tyrosine kinase inhibitors (TKIs). Several of these novel ALK fusion variants were identified as being resistant to EGFR TKIs or as dual 3’ALK fusions. In addition, at least 28 intergenic ALK rearrangements have also been reported, with three of them reported as responding to crizotinib. This review aims to serve as a central source of reference of fusion partners in ALK+ NSCLC for clinicians and scientists. We aim to update and improve the list going forward. Elsevier 2020-02-19 /pmc/articles/PMC8474466/ /pubmed/34589917 http://dx.doi.org/10.1016/j.jtocrr.2020.100015 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Ou, Sai-Hong Ignatius
Zhu, Viola W.
Nagasaka, Misako
Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020
title Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020
title_full Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020
title_fullStr Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020
title_full_unstemmed Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020
title_short Catalog of 5’ Fusion Partners in ALK-positive NSCLC Circa 2020
title_sort catalog of 5’ fusion partners in alk-positive nsclc circa 2020
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8474466/
https://www.ncbi.nlm.nih.gov/pubmed/34589917
http://dx.doi.org/10.1016/j.jtocrr.2020.100015
work_keys_str_mv AT ousaihongignatius catalogof5fusionpartnersinalkpositivensclccirca2020
AT zhuviolaw catalogof5fusionpartnersinalkpositivensclccirca2020
AT nagasakamisako catalogof5fusionpartnersinalkpositivensclccirca2020