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Wobble uridine tRNA modification: a new vulnerability of refractory melanoma
The enzymes catalysing the modification of the wobble uridine (U(34)) of tRNAs (U(34)-enzymes) play an important role in tumor development. We have recently demonstrated that the U(34)-enzymes are crucial in the survival of glycolytic melanoma cultures through a codon-specific regulation of HIF1α mR...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276846/ https://www.ncbi.nlm.nih.gov/pubmed/30525092 http://dx.doi.org/10.1080/23723556.2018.1513725 |
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author | Rapino, Francesca Close, Pierre |
author_facet | Rapino, Francesca Close, Pierre |
author_sort | Rapino, Francesca |
collection | PubMed |
description | The enzymes catalysing the modification of the wobble uridine (U(34)) of tRNAs (U(34)-enzymes) play an important role in tumor development. We have recently demonstrated that the U(34)-enzymes are crucial in the survival of glycolytic melanoma cultures through a codon-specific regulation of HIF1α mRNA translation. Moreover, depletion of U(34)-enzymes resensitizes resistant melanoma to targeted therapy. These results indicate that targeting U(34)-enzymes represents a new therapeutic opportunity for melanoma patients. |
format | Online Article Text |
id | pubmed-6276846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-62768462019-09-25 Wobble uridine tRNA modification: a new vulnerability of refractory melanoma Rapino, Francesca Close, Pierre Mol Cell Oncol Commentary The enzymes catalysing the modification of the wobble uridine (U(34)) of tRNAs (U(34)-enzymes) play an important role in tumor development. We have recently demonstrated that the U(34)-enzymes are crucial in the survival of glycolytic melanoma cultures through a codon-specific regulation of HIF1α mRNA translation. Moreover, depletion of U(34)-enzymes resensitizes resistant melanoma to targeted therapy. These results indicate that targeting U(34)-enzymes represents a new therapeutic opportunity for melanoma patients. Taylor & Francis 2018-09-25 /pmc/articles/PMC6276846/ /pubmed/30525092 http://dx.doi.org/10.1080/23723556.2018.1513725 Text en © 2018 The Author(s). Published by Taylor & Francis. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Commentary Rapino, Francesca Close, Pierre Wobble uridine tRNA modification: a new vulnerability of refractory melanoma |
title | Wobble uridine tRNA modification: a new vulnerability of refractory melanoma |
title_full | Wobble uridine tRNA modification: a new vulnerability of refractory melanoma |
title_fullStr | Wobble uridine tRNA modification: a new vulnerability of refractory melanoma |
title_full_unstemmed | Wobble uridine tRNA modification: a new vulnerability of refractory melanoma |
title_short | Wobble uridine tRNA modification: a new vulnerability of refractory melanoma |
title_sort | wobble uridine trna modification: a new vulnerability of refractory melanoma |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6276846/ https://www.ncbi.nlm.nih.gov/pubmed/30525092 http://dx.doi.org/10.1080/23723556.2018.1513725 |
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