Cancer is characterized by pervasive epigenetic alterations with enhancer dysfunction orchestrating the aberrant cancer transcriptional programs and transcriptional dependencies. Here, we epigenetically characterize human colorectal cancer (CRC) using de novo chromatin state discovery on a library of different patient-derived organoids. By exploring this resource, we unveil a tumor-specific deregulated enhancerome that is cancer cell-intrinsic and independent of interpatient heterogeneity. We show that the transcriptional coactivators YAP/TAZ act as key regulators of the conserved CRC gained enhancers. The same YAP/TAZ-bound enhancers display active chromatin profiles across diverse human tumors, highlighting a pan-cancer epigenetic rewiring which at single-cell level distinguishes malignant from normal cell populations. YAP/TAZ inhibition in established tumor organoids causes extensive cell death unveiling their essential role in tumor maintenance. This work indicates a common layer of YAP/TAZ-fueled enhancer reprogramming that is key for the cancer cell state and can be exploited for the development of improved therapeutic avenues.

Epigenomic landscape of human colorectal cancer unveils an aberrant core of pan-cancer enhancers orchestrated by YAP/TAZ / G. Della Chiara, F. Gervasoni, M. Fakiola, C. Godano, C. D'Oria, L. Azzolin, R.J.P. Bonnal, G. Moreni, L. Drufuca, G. Rossetti, V. Ranzani, R. Bason, M. De Simone, F. Panariello, I. Ferrari, T. Fabbris, F. Zanconato, M. Forcato, O. Romano, J. Caroli, P. Gruarin, M.L. Sarnicola, M. Cordenonsi, A. Bardelli, N. Zucchini, A.P. Ceretti, N.M. Mariani, A. Cassingena, A. Sartore-Bianchi, G. Testa, L. Gianotti, E. Opocher, F. Pisati, C. Tripodo, G. Macino, S. Siena, S. Bicciato, S. Piccolo, M. Pagani. - In: NATURE COMMUNICATIONS. - ISSN 2041-1723. - 12:1(2021 Apr 20), pp. 2340.1-2340.18. [10.1038/s41467-021-22544-y]

Epigenomic landscape of human colorectal cancer unveils an aberrant core of pan-cancer enhancers orchestrated by YAP/TAZ

G. Della Chiara
Primo
;
F. Gervasoni
Secondo
;
M. Fakiola;C. Godano;C. D'Oria;L. Drufuca;V. Ranzani;R. Bason;M. De Simone;F. Panariello;I. Ferrari;T. Fabbris;N.M. Mariani;A. Sartore-Bianchi;G. Testa;E. Opocher;F. Pisati;C. Tripodo;S. Siena;M. Pagani
2021

Abstract

Cancer is characterized by pervasive epigenetic alterations with enhancer dysfunction orchestrating the aberrant cancer transcriptional programs and transcriptional dependencies. Here, we epigenetically characterize human colorectal cancer (CRC) using de novo chromatin state discovery on a library of different patient-derived organoids. By exploring this resource, we unveil a tumor-specific deregulated enhancerome that is cancer cell-intrinsic and independent of interpatient heterogeneity. We show that the transcriptional coactivators YAP/TAZ act as key regulators of the conserved CRC gained enhancers. The same YAP/TAZ-bound enhancers display active chromatin profiles across diverse human tumors, highlighting a pan-cancer epigenetic rewiring which at single-cell level distinguishes malignant from normal cell populations. YAP/TAZ inhibition in established tumor organoids causes extensive cell death unveiling their essential role in tumor maintenance. This work indicates a common layer of YAP/TAZ-fueled enhancer reprogramming that is key for the cancer cell state and can be exploited for the development of improved therapeutic avenues.
Adaptor Proteins, Signal Transducing; Colorectal Neoplasms; Gene Expression Regulation, Neoplastic; Histone Code; Humans; Models, Genetic; Organoids; RNA-Seq; Single-Cell Analysis; Trans-Activators; Transcription Factors; Transcriptional Coactivator with PDZ-Binding Motif Proteins; Tumor Cells, Cultured; YAP-Signaling Proteins; Enhancer Elements, Genetic; Epigenesis, Genetic
Settore BIO/11 - Biologia Molecolare
Settore BIOS-08/A - Biologia molecolare
Settore BIOS-14/A - Genetica
   Long non-coding RNAs of tumor infiltrating lymphocytes as novel anti-cancer therapeutic targets
   FIGHT-CANCER
   EUROPEAN COMMISSION
   FP7
   617978
20-apr-2021
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/945934
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