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Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells

In embryonic stem cells, promoters of key lineage-specific differentiation genes are found in a bivalent state, having both activating H3K4me3 and repressive H3K27me3 histone marks, making them poised for transcription upon loss of H3K27me3. Whether cancer-initiating cells (C-ICs) have similar epige...

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Autores principales: Lima-Fernandes, Evelyne, Murison, Alex, da Silva Medina, Tiago, Wang, Yadong, Ma, Anqi, Leung, Cherry, Luciani, Genna M., Haynes, Jennifer, Pollett, Aaron, Zeller, Constanze, Duan, Shili, Kreso, Antonija, Barsyte-Lovejoy, Dalia, Wouters, Bradly G., Jin, Jian, Carvalho, Daniel D. De, Lupien, Mathieu, Arrowsmith, Cheryl H., O’Brien, Catherine A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441108/
https://www.ncbi.nlm.nih.gov/pubmed/30926792
http://dx.doi.org/10.1038/s41467-019-09309-4
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author Lima-Fernandes, Evelyne
Murison, Alex
da Silva Medina, Tiago
Wang, Yadong
Ma, Anqi
Leung, Cherry
Luciani, Genna M.
Haynes, Jennifer
Pollett, Aaron
Zeller, Constanze
Duan, Shili
Kreso, Antonija
Barsyte-Lovejoy, Dalia
Wouters, Bradly G.
Jin, Jian
Carvalho, Daniel D. De
Lupien, Mathieu
Arrowsmith, Cheryl H.
O’Brien, Catherine A.
author_facet Lima-Fernandes, Evelyne
Murison, Alex
da Silva Medina, Tiago
Wang, Yadong
Ma, Anqi
Leung, Cherry
Luciani, Genna M.
Haynes, Jennifer
Pollett, Aaron
Zeller, Constanze
Duan, Shili
Kreso, Antonija
Barsyte-Lovejoy, Dalia
Wouters, Bradly G.
Jin, Jian
Carvalho, Daniel D. De
Lupien, Mathieu
Arrowsmith, Cheryl H.
O’Brien, Catherine A.
author_sort Lima-Fernandes, Evelyne
collection PubMed
description In embryonic stem cells, promoters of key lineage-specific differentiation genes are found in a bivalent state, having both activating H3K4me3 and repressive H3K27me3 histone marks, making them poised for transcription upon loss of H3K27me3. Whether cancer-initiating cells (C-ICs) have similar epigenetic mechanisms that prevent lineage commitment is unknown. Here we show that colorectal C-ICs (CC-ICs) are maintained in a stem-like state through a bivalent epigenetic mechanism. Disruption of the bivalent state through inhibition of the H3K27 methyltransferase EZH2, resulted in decreased self-renewal of patient-derived C-ICs. Epigenomic analyses revealed that the promoter of Indian Hedgehog (IHH), a canonical driver of normal colonocyte differentiation, exists in a bivalent chromatin state. Inhibition of EZH2 resulted in de-repression of IHH, decreased self-renewal, and increased sensitivity to chemotherapy in vivo. Our results reveal an epigenetic block to differentiation in CC-ICs and demonstrate the potential for epigenetic differentiation therapy of a solid tumour through EZH2 inhibition.
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spelling pubmed-64411082019-04-01 Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells Lima-Fernandes, Evelyne Murison, Alex da Silva Medina, Tiago Wang, Yadong Ma, Anqi Leung, Cherry Luciani, Genna M. Haynes, Jennifer Pollett, Aaron Zeller, Constanze Duan, Shili Kreso, Antonija Barsyte-Lovejoy, Dalia Wouters, Bradly G. Jin, Jian Carvalho, Daniel D. De Lupien, Mathieu Arrowsmith, Cheryl H. O’Brien, Catherine A. Nat Commun Article In embryonic stem cells, promoters of key lineage-specific differentiation genes are found in a bivalent state, having both activating H3K4me3 and repressive H3K27me3 histone marks, making them poised for transcription upon loss of H3K27me3. Whether cancer-initiating cells (C-ICs) have similar epigenetic mechanisms that prevent lineage commitment is unknown. Here we show that colorectal C-ICs (CC-ICs) are maintained in a stem-like state through a bivalent epigenetic mechanism. Disruption of the bivalent state through inhibition of the H3K27 methyltransferase EZH2, resulted in decreased self-renewal of patient-derived C-ICs. Epigenomic analyses revealed that the promoter of Indian Hedgehog (IHH), a canonical driver of normal colonocyte differentiation, exists in a bivalent chromatin state. Inhibition of EZH2 resulted in de-repression of IHH, decreased self-renewal, and increased sensitivity to chemotherapy in vivo. Our results reveal an epigenetic block to differentiation in CC-ICs and demonstrate the potential for epigenetic differentiation therapy of a solid tumour through EZH2 inhibition. Nature Publishing Group UK 2019-03-29 /pmc/articles/PMC6441108/ /pubmed/30926792 http://dx.doi.org/10.1038/s41467-019-09309-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lima-Fernandes, Evelyne
Murison, Alex
da Silva Medina, Tiago
Wang, Yadong
Ma, Anqi
Leung, Cherry
Luciani, Genna M.
Haynes, Jennifer
Pollett, Aaron
Zeller, Constanze
Duan, Shili
Kreso, Antonija
Barsyte-Lovejoy, Dalia
Wouters, Bradly G.
Jin, Jian
Carvalho, Daniel D. De
Lupien, Mathieu
Arrowsmith, Cheryl H.
O’Brien, Catherine A.
Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
title Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
title_full Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
title_fullStr Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
title_full_unstemmed Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
title_short Targeting bivalency de-represses Indian Hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
title_sort targeting bivalency de-represses indian hedgehog and inhibits self-renewal of colorectal cancer-initiating cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441108/
https://www.ncbi.nlm.nih.gov/pubmed/30926792
http://dx.doi.org/10.1038/s41467-019-09309-4
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