Ring1b-dependent epigenetic remodelling is an essential prerequisite for pancreatic carcinogenesis.


Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
11 2019
Historique:
received: 18 07 2018
revised: 08 02 2019
accepted: 24 02 2019
pubmed: 8 4 2019
medline: 2 11 2019
entrez: 8 4 2019
Statut: ppublish

Résumé

Besides well-defined genetic alterations, the dedifferentiation of mature acinar cells is an important prerequisite for pancreatic carcinogenesis. Acinar-specific genes controlling cell homeostasis are extensively downregulated during cancer development; however, the underlying mechanisms are poorly understood. Now, we devised a novel in vitro strategy to determine genome-wide dynamics in the epigenetic landscape in pancreatic carcinogenesis. With our in vitro carcinogenic sequence, we performed global gene expression analysis and ChIP sequencing for the histone modifications H3K4me3, H3K27me3 and H2AK119ub. Followed by a comprehensive bioinformatic approach, we captured gene clusters with extensive epigenetic and transcriptional remodelling. Relevance of Ring1b-catalysed H2AK119ub in acinar cell reprogramming was studied in an inducible Ring1b knockout mouse model. CRISPR/Cas9-mediated Ring1b ablation as well as drug-induced Ring1b inhibition were functionally characterised in pancreatic cancer cells. The epigenome is vigorously modified during pancreatic carcinogenesis, defining cellular identity. Particularly, regulatory acinar cell transcription factors are epigenetically silenced by the Ring1b-catalysed histone modification H2AK119ub in acinar-to-ductal metaplasia and pancreatic cancer cells. Ring1b knockout mice showed greatly impaired acinar cell dedifferentiation and pancreatic tumour formation due to a retained expression of acinar differentiation genes. Depletion or drug-induced inhibition of Ring1b promoted tumour cell reprogramming towards a less aggressive phenotype. Our data provide substantial evidence that the epigenetic silencing of acinar cell fate genes is a mandatory event in the development and progression of pancreatic cancer. Targeting the epigenetic repressor Ring1b could offer new therapeutic options.

Sections du résumé

BACKGROUND AND AIMS
Besides well-defined genetic alterations, the dedifferentiation of mature acinar cells is an important prerequisite for pancreatic carcinogenesis. Acinar-specific genes controlling cell homeostasis are extensively downregulated during cancer development; however, the underlying mechanisms are poorly understood. Now, we devised a novel in vitro strategy to determine genome-wide dynamics in the epigenetic landscape in pancreatic carcinogenesis.
DESIGN
With our in vitro carcinogenic sequence, we performed global gene expression analysis and ChIP sequencing for the histone modifications H3K4me3, H3K27me3 and H2AK119ub. Followed by a comprehensive bioinformatic approach, we captured gene clusters with extensive epigenetic and transcriptional remodelling. Relevance of Ring1b-catalysed H2AK119ub in acinar cell reprogramming was studied in an inducible Ring1b knockout mouse model. CRISPR/Cas9-mediated Ring1b ablation as well as drug-induced Ring1b inhibition were functionally characterised in pancreatic cancer cells.
RESULTS
The epigenome is vigorously modified during pancreatic carcinogenesis, defining cellular identity. Particularly, regulatory acinar cell transcription factors are epigenetically silenced by the Ring1b-catalysed histone modification H2AK119ub in acinar-to-ductal metaplasia and pancreatic cancer cells. Ring1b knockout mice showed greatly impaired acinar cell dedifferentiation and pancreatic tumour formation due to a retained expression of acinar differentiation genes. Depletion or drug-induced inhibition of Ring1b promoted tumour cell reprogramming towards a less aggressive phenotype.
CONCLUSIONS
Our data provide substantial evidence that the epigenetic silencing of acinar cell fate genes is a mandatory event in the development and progression of pancreatic cancer. Targeting the epigenetic repressor Ring1b could offer new therapeutic options.

Identifiants

pubmed: 30954952
pii: gutjnl-2018-317208
doi: 10.1136/gutjnl-2018-317208
doi:

Substances chimiques

Polycomb Repressive Complex 1 EC 2.3.2.27
Rnf2 protein, mouse EC 2.3.2.27
Ubiquitin-Protein Ligases EC 2.3.2.27

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2007-2018

Informations de copyright

© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Simone Benitz (S)

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.
Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.

Tobias Straub (T)

Bioinformatic Unit, Biomedical Center, Faculty of Medicine, LMU Munich, Munich, Germany.

Ujjwal Mukund Mahajan (UM)

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.

Jurik Mutter (J)

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.

Stefan Czemmel (S)

Quantitative Biology Center, University of Tuebingen, Tuebingen, Germany.

Tatjana Unruh (T)

Institute of Pathology, Heinrich-Heine University and University Hospital, Duesseldorf, Germany.

Britta Wingerath (B)

Institute of Pathology, Heinrich-Heine University and University Hospital, Duesseldorf, Germany.

Sabrina Deubler (S)

Department of Surgery, Technical University Munich, Munich, Germany.

Lisa Fahr (L)

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.

Tao Cheng (T)

Department of Surgery, Technical University Munich, Munich, Germany.

Sven Nahnsen (S)

Quantitative Biology Center, University of Tuebingen, Tuebingen, Germany.

Philipp Bruns (P)

Department of Surgery, Technical University Munich, Munich, Germany.

Bo Kong (B)

Department of Surgery, Technical University Munich, Munich, Germany.

Susanne Raulefs (S)

Department of Surgery, Technical University Munich, Munich, Germany.

Güralp O Ceyhan (GO)

Department of Surgery, Technical University Munich, Munich, Germany.

Julia Mayerle (J)

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.

Katja Steiger (K)

Institute of Pathology, Technical University Munich, Munich, Germany.

Irene Esposito (I)

Institute of Pathology, Heinrich-Heine-Universitat Dusseldorf, Dusseldorf, Germany.

Jörg Kleeff (J)

Department of Surgery, Martin-Luther University Halle-Wittenberg, Halle (Saale), Germany.

Christoph W Michalski (CW)

Department of Surgery, Martin-Luther University Halle-Wittenberg, Halle (Saale), Germany.

Ivonne Regel (I)

Department of Medicine II, University Hospital, LMU Munich, Munich, Germany.

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