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Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors

The histone methyltransferase Enhancer of Zeste Homolog 2 (EZH2) is frequently dysregulated in cancers, and gain-of-function (GOF) EZH2 mutations have been identified in non-Hodgkin lymphomas. Small-molecule inhibitors against EZH2 demonstrated anti-tumor activity in EZH2-mutated lymphomas and enter...

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Autores principales: Gibaja, V, Shen, F, Harari, J, Korn, J, Ruddy, D, Saenz-Vash, V, Zhai, H, Rejtar, T, Paris, C G, Yu, Z, Lira, M, King, D, Qi, W, Keen, N, Hassan, A Q, Chan, H M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744243/
https://www.ncbi.nlm.nih.gov/pubmed/25893294
http://dx.doi.org/10.1038/onc.2015.114
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author Gibaja, V
Shen, F
Harari, J
Korn, J
Ruddy, D
Saenz-Vash, V
Zhai, H
Rejtar, T
Paris, C G
Yu, Z
Lira, M
King, D
Qi, W
Keen, N
Hassan, A Q
Chan, H M
author_facet Gibaja, V
Shen, F
Harari, J
Korn, J
Ruddy, D
Saenz-Vash, V
Zhai, H
Rejtar, T
Paris, C G
Yu, Z
Lira, M
King, D
Qi, W
Keen, N
Hassan, A Q
Chan, H M
author_sort Gibaja, V
collection PubMed
description The histone methyltransferase Enhancer of Zeste Homolog 2 (EZH2) is frequently dysregulated in cancers, and gain-of-function (GOF) EZH2 mutations have been identified in non-Hodgkin lymphomas. Small-molecule inhibitors against EZH2 demonstrated anti-tumor activity in EZH2-mutated lymphomas and entered clinical trials. Here, we developed models of acquired resistance to EZH2 inhibitor EI1 with EZH2-mutated lymphoma cells. Resistance was generated by secondary mutations in both wild-type (WT) and GOF Y641N EZH2 alleles. These EZH2 mutants retained the substrate specificity of their predecessor complexes but became refractory to biochemical inhibition by EZH2 inhibitors. Resistant cells were able to maintain a high level of H3K27Me3 in the presence of inhibitors. Interestingly, mutation of EZH2 WT alone generated an intermediate resistance phenotype, which is consistent with a previously proposed model of cooperation between EZH2 WT and Y641N mutants to promote tumorigenesis. In addition, the findings presented here have implications for the clinical translation of EZH2 inhibitors and underscore the need to develop novel EZH2 inhibitors to target potential resistance emerging in clinical settings.
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spelling pubmed-47442432016-02-23 Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors Gibaja, V Shen, F Harari, J Korn, J Ruddy, D Saenz-Vash, V Zhai, H Rejtar, T Paris, C G Yu, Z Lira, M King, D Qi, W Keen, N Hassan, A Q Chan, H M Oncogene Original Article The histone methyltransferase Enhancer of Zeste Homolog 2 (EZH2) is frequently dysregulated in cancers, and gain-of-function (GOF) EZH2 mutations have been identified in non-Hodgkin lymphomas. Small-molecule inhibitors against EZH2 demonstrated anti-tumor activity in EZH2-mutated lymphomas and entered clinical trials. Here, we developed models of acquired resistance to EZH2 inhibitor EI1 with EZH2-mutated lymphoma cells. Resistance was generated by secondary mutations in both wild-type (WT) and GOF Y641N EZH2 alleles. These EZH2 mutants retained the substrate specificity of their predecessor complexes but became refractory to biochemical inhibition by EZH2 inhibitors. Resistant cells were able to maintain a high level of H3K27Me3 in the presence of inhibitors. Interestingly, mutation of EZH2 WT alone generated an intermediate resistance phenotype, which is consistent with a previously proposed model of cooperation between EZH2 WT and Y641N mutants to promote tumorigenesis. In addition, the findings presented here have implications for the clinical translation of EZH2 inhibitors and underscore the need to develop novel EZH2 inhibitors to target potential resistance emerging in clinical settings. Nature Publishing Group 2016-02-04 2015-04-20 /pmc/articles/PMC4744243/ /pubmed/25893294 http://dx.doi.org/10.1038/onc.2015.114 Text en Copyright © 2016 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Original Article
Gibaja, V
Shen, F
Harari, J
Korn, J
Ruddy, D
Saenz-Vash, V
Zhai, H
Rejtar, T
Paris, C G
Yu, Z
Lira, M
King, D
Qi, W
Keen, N
Hassan, A Q
Chan, H M
Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors
title Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors
title_full Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors
title_fullStr Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors
title_full_unstemmed Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors
title_short Development of secondary mutations in wild-type and mutant EZH2 alleles cooperates to confer resistance to EZH2 inhibitors
title_sort development of secondary mutations in wild-type and mutant ezh2 alleles cooperates to confer resistance to ezh2 inhibitors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4744243/
https://www.ncbi.nlm.nih.gov/pubmed/25893294
http://dx.doi.org/10.1038/onc.2015.114
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