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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Nature Portfolio
2019
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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) |
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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 |
work_keys_str_mv |
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