Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/25684
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dc.contributor.authorSbirkov, Yordan-
dc.contributor.authorKwok, Colin-
dc.contributor.authorBhamra, Amandeep-
dc.contributor.authorThompson, Andrew J-
dc.contributor.authorGil, Veronica-
dc.contributor.authorZelent, Arthur-
dc.contributor.authorPetrie, Kevin-
dc.date.accessioned2017-09-23T02:03:03Z-
dc.date.available2017-09-23T02:03:03Z-
dc.date.issued2017-07-05-
dc.identifier.other1440-
dc.identifier.urihttp://hdl.handle.net/1893/25684-
dc.description.abstractAlterations to the gene encoding the EZH2 (KMT6A) methyltransferase, including both gain-of-function and loss-of-function, have been linked to a variety of haematological malignancies and solid tumours, suggesting a complex, context-dependent role of this methyltransferase. The successful implementation of molecularly targeted therapies against EZH2 requires a greater understanding of the potential mechanisms by which EZH2 contributes to cancer. One aspect of this effort is the mapping of EZH2 partner proteins and cellular targets. To this end we performed affinity-purification mass spectrometry in the FAB-M2 HL-60 acute myeloid leukaemia (AML) cell line before and after all-transretinoic acid-induced differentiation. These studies identified new EZH2 interaction partners and potential non-histone substrates for EZH2-mediated methylation. Our results suggest that EZH2 is involved in the regulation of translation through interactions with a number of RNA binding proteins and by methylating key components of protein synthesis such as eEF1A1. Given that deregulated mRNA translation is a frequent feature of cancer and that eEF1A1 is highly expressed in many human tumours, these findings present new possibilities for the therapeutic targeting of EZH2 in AML.en_UK
dc.language.isoen-
dc.publisherMDPI-
dc.relationSbirkov Y, Kwok C, Bhamra A, Thompson AJ, Gil V, Zelent A & Petrie K (2017) Semi-quantitative mass spectrometry in AML cells identifies new non-genomic targets of the EZH2 methyltransferase, International Journal of Molecular Sciences, 18 (7), Art. No.: 1440.-
dc.rights© 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).-
dc.subjectacute myeloid leukaemiaen_UK
dc.subjectEZH2en_UK
dc.subjectmass spectrometryen_UK
dc.subjectmethylationen_UK
dc.subjecteEF1A1en_UK
dc.titleSemi-quantitative mass spectrometry in AML cells identifies new non-genomic targets of the EZH2 methyltransferaseen_UK
dc.typeJournal Articleen_UK
dc.identifier.doihttp://dx.doi.org/10.3390/ijms18071440-
dc.identifier.pmid28678185-
dc.citation.jtitleInternational Journal of Molecular Sciences-
dc.citation.issn1661-6596-
dc.citation.volume18-
dc.citation.issue7-
dc.citation.publicationstatusPublished-
dc.citation.peerreviewedRefereed-
dc.type.statusPublisher version (final published refereed version)-
dc.citation.date05/07/2017-
dc.contributor.affiliationJulius Maximilians University of Wurzburg-
dc.contributor.affiliationInstitute of Cancer Research-
dc.contributor.affiliationUniversity College London-
dc.contributor.affiliationInstitute of Cancer Research-
dc.contributor.affiliationInstitute of Cancer Research-
dc.contributor.affiliationUniversity of Miami, USA-
dc.contributor.affiliationBiological and Environmental Sciences-
dc.identifier.isi000408746800110-
Appears in Collections:Biological and Environmental Sciences Journal Articles

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