An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells

Melanoma persister cells are tolerant to anti-BRAF and anti-MEK inhibition and can trigger cancer relapse. Here the authors show that a subset of N6-methyladenosine modified mRNAs is translationally activated in persister cells. This preferential translation can be abrogated via eIF4A inhibition.

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Autores principales: Shensi Shen, Sara Faouzi, Amandine Bastide, Sylvain Martineau, Hélène Malka-Mahieu, Yu Fu, Xiaoxiao Sun, Christine Mateus, Emilie Routier, Severine Roy, Laurent Desaubry, Fabrice André, Alexander Eggermont, Alexandre David, Jean-Yves Scoazec, Stéphan Vagner, Caroline Robert
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Lenguaje:EN
Publicado: Nature Portfolio 2019
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Acceso en línea:https://doaj.org/article/e47491eb7c3744b2a9a1e54104826b8f
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spelling oai:doaj.org-article:e47491eb7c3744b2a9a1e54104826b8f2021-12-02T17:33:10ZAn epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells10.1038/s41467-019-13360-62041-1723https://doaj.org/article/e47491eb7c3744b2a9a1e54104826b8f2019-12-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-13360-6https://doaj.org/toc/2041-1723Melanoma persister cells are tolerant to anti-BRAF and anti-MEK inhibition and can trigger cancer relapse. Here the authors show that a subset of N6-methyladenosine modified mRNAs is translationally activated in persister cells. This preferential translation can be abrogated via eIF4A inhibition.Shensi ShenSara FaouziAmandine BastideSylvain MartineauHélène Malka-MahieuYu FuXiaoxiao SunChristine MateusEmilie RoutierSeverine RoyLaurent DesaubryFabrice AndréAlexander EggermontAlexandre DavidJean-Yves ScoazecStéphan VagnerCaroline RobertNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Shensi Shen
Sara Faouzi
Amandine Bastide
Sylvain Martineau
Hélène Malka-Mahieu
Yu Fu
Xiaoxiao Sun
Christine Mateus
Emilie Routier
Severine Roy
Laurent Desaubry
Fabrice André
Alexander Eggermont
Alexandre David
Jean-Yves Scoazec
Stéphan Vagner
Caroline Robert
An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
description Melanoma persister cells are tolerant to anti-BRAF and anti-MEK inhibition and can trigger cancer relapse. Here the authors show that a subset of N6-methyladenosine modified mRNAs is translationally activated in persister cells. This preferential translation can be abrogated via eIF4A inhibition.
format article
author Shensi Shen
Sara Faouzi
Amandine Bastide
Sylvain Martineau
Hélène Malka-Mahieu
Yu Fu
Xiaoxiao Sun
Christine Mateus
Emilie Routier
Severine Roy
Laurent Desaubry
Fabrice André
Alexander Eggermont
Alexandre David
Jean-Yves Scoazec
Stéphan Vagner
Caroline Robert
author_facet Shensi Shen
Sara Faouzi
Amandine Bastide
Sylvain Martineau
Hélène Malka-Mahieu
Yu Fu
Xiaoxiao Sun
Christine Mateus
Emilie Routier
Severine Roy
Laurent Desaubry
Fabrice André
Alexander Eggermont
Alexandre David
Jean-Yves Scoazec
Stéphan Vagner
Caroline Robert
author_sort Shensi Shen
title An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
title_short An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
title_full An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
title_fullStr An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
title_full_unstemmed An epitranscriptomic mechanism underlies selective mRNA translation remodelling in melanoma persister cells
title_sort epitranscriptomic mechanism underlies selective mrna translation remodelling in melanoma persister cells
publisher Nature Portfolio
publishDate 2019
url https://doaj.org/article/e47491eb7c3744b2a9a1e54104826b8f
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