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MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples

MET exon 14 skipping ( METΔ14 ) is a well-characterized oncogene in the Ras-MAPK pathway driving lung adenocarcinoma (LUAD). Previous studies on METΔ14 revealed this aberrantly spliced oncogene is expressed in LUAD primary samples and is associated with heterozygous somatic mutations and deletions n...

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Autores principales: Durham, Megan, Vadde, Swetha, Brooks, Angela N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565573/
https://www.ncbi.nlm.nih.gov/pubmed/37829573
http://dx.doi.org/10.17912/micropub.biology.000957
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author Durham, Megan
Vadde, Swetha
Brooks, Angela N
author_facet Durham, Megan
Vadde, Swetha
Brooks, Angela N
author_sort Durham, Megan
collection PubMed
description MET exon 14 skipping ( METΔ14 ) is a well-characterized oncogene in the Ras-MAPK pathway driving lung adenocarcinoma (LUAD). Previous studies on METΔ14 revealed this aberrantly spliced oncogene is expressed in LUAD primary samples and is associated with heterozygous somatic mutations and deletions near exon 14 splice sites. Upon further examination of DNA and RNA sequencing data from primary samples, we highlight that METΔ14 is overexpressed in an allele-specific manner. These data suggest that dose-dependence of METΔ14 may be critical to oncogenesis.
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spelling pubmed-105655732023-10-12 MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples Durham, Megan Vadde, Swetha Brooks, Angela N MicroPubl Biol New Finding MET exon 14 skipping ( METΔ14 ) is a well-characterized oncogene in the Ras-MAPK pathway driving lung adenocarcinoma (LUAD). Previous studies on METΔ14 revealed this aberrantly spliced oncogene is expressed in LUAD primary samples and is associated with heterozygous somatic mutations and deletions near exon 14 splice sites. Upon further examination of DNA and RNA sequencing data from primary samples, we highlight that METΔ14 is overexpressed in an allele-specific manner. These data suggest that dose-dependence of METΔ14 may be critical to oncogenesis. Caltech Library 2023-09-26 /pmc/articles/PMC10565573/ /pubmed/37829573 http://dx.doi.org/10.17912/micropub.biology.000957 Text en Copyright: © 2023 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle New Finding
Durham, Megan
Vadde, Swetha
Brooks, Angela N
MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
title MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
title_full MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
title_fullStr MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
title_full_unstemmed MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
title_short MET exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
title_sort met exon 14 skipping is overexpressed in an allele-specific manner in lung adenocarcinoma primary samples
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565573/
https://www.ncbi.nlm.nih.gov/pubmed/37829573
http://dx.doi.org/10.17912/micropub.biology.000957
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