PARP inhibitors and radiation potentiate liver cell death in vitro. Do hepatocellular carcinomas have an achilles' heel?


Journal

Clinics and research in hepatology and gastroenterology
ISSN: 2210-741X
Titre abrégé: Clin Res Hepatol Gastroenterol
Pays: France
ID NLM: 101553659

Informations de publication

Date de publication:
09 2021
Historique:
received: 24 06 2020
revised: 10 09 2020
accepted: 30 09 2020
pubmed: 14 11 2020
medline: 3 3 2022
entrez: 13 11 2020
Statut: ppublish

Résumé

A promising avenue for cancer treatment is exacerbating the deregulation of the DNA repair machinery that would normally protect the genome. To address the applicability of poly(ADP-ribose) polymerase (PARP) inhibitors (PARPi) combined with radiotherapy for the treatment of hepatocellular carcinoma (HCC) two approaches were used: firstly, the in vitro sensitivity to the PARPi Veliparib and Talazoparib +/- radiation exposure was determined in liver cell lines and the impact of the HBV X protein (HBx) that deregulates cellular DNA damage repair via SMC5/6 degradation was investigated. Secondly, PARP expression profiles and DNA damage levels using the surrogate marker gammaH2AX were assessed in a panel of control liver vs HCC tissues. Cell cytotoxicity was measured by clonogenic survival or relative cell growth and the DNA damage response using immunological-based techniques in Hep3B, PLC/PRF/5, HepG2- and HepaRG-derived models. Transcriptome changes due to HBx expression vs SMC6 loss were assessed by RNA sequencing in HepaRG-derived models. PARP and PARG transcripts (qPCR) and PARP1, H2AX and gammaH2AX protein levels (RPPA) were compared in control liver vs HBV-, HCV-, alcohol- and non-alcoholic steatohepatitis-associated HCC (tumor/peritumor) tissues. PARPi cytotoxicity was significantly enhanced when combined with X-rays (2Gy) with Talazoparib having a greater impact than Veliparib in most in vitro models. HBx expression significantly lowered survival, probably driven by SMC5/6 loss based on the transcriptome analysis and higher DNA damage levels. PARP1 and PARP2 transcript levels were significantly higher in tumor than peritumor and control tissues. The HBV/HCV/alcohol-associated tumor tissues studied had reduced H2AX but higher gammaH2AX protein levels compared to peritumor and control tissues providing evidence of increased DNA damage during liver disease progression. These proof-of-concept experiments support PARPi alone or combined with radiotherapy for HCC treatment, particularly for HBV-associated tumors, that warrant further investigation.

Sections du résumé

BACKGROUND
A promising avenue for cancer treatment is exacerbating the deregulation of the DNA repair machinery that would normally protect the genome. To address the applicability of poly(ADP-ribose) polymerase (PARP) inhibitors (PARPi) combined with radiotherapy for the treatment of hepatocellular carcinoma (HCC) two approaches were used: firstly, the in vitro sensitivity to the PARPi Veliparib and Talazoparib +/- radiation exposure was determined in liver cell lines and the impact of the HBV X protein (HBx) that deregulates cellular DNA damage repair via SMC5/6 degradation was investigated. Secondly, PARP expression profiles and DNA damage levels using the surrogate marker gammaH2AX were assessed in a panel of control liver vs HCC tissues.
METHODS
Cell cytotoxicity was measured by clonogenic survival or relative cell growth and the DNA damage response using immunological-based techniques in Hep3B, PLC/PRF/5, HepG2- and HepaRG-derived models. Transcriptome changes due to HBx expression vs SMC6 loss were assessed by RNA sequencing in HepaRG-derived models. PARP and PARG transcripts (qPCR) and PARP1, H2AX and gammaH2AX protein levels (RPPA) were compared in control liver vs HBV-, HCV-, alcohol- and non-alcoholic steatohepatitis-associated HCC (tumor/peritumor) tissues.
RESULTS
PARPi cytotoxicity was significantly enhanced when combined with X-rays (2Gy) with Talazoparib having a greater impact than Veliparib in most in vitro models. HBx expression significantly lowered survival, probably driven by SMC5/6 loss based on the transcriptome analysis and higher DNA damage levels. PARP1 and PARP2 transcript levels were significantly higher in tumor than peritumor and control tissues. The HBV/HCV/alcohol-associated tumor tissues studied had reduced H2AX but higher gammaH2AX protein levels compared to peritumor and control tissues providing evidence of increased DNA damage during liver disease progression.
CONCLUSIONS
These proof-of-concept experiments support PARPi alone or combined with radiotherapy for HCC treatment, particularly for HBV-associated tumors, that warrant further investigation.

Identifiants

pubmed: 33183998
pii: S2210-7401(20)30294-1
doi: 10.1016/j.clinre.2020.09.014
pii:
doi:

Substances chimiques

Poly(ADP-ribose) Polymerase Inhibitors 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

101553

Informations de copyright

Copyright © 2020. Published by Elsevier Masson SAS.

Auteurs

Laetitia Gerossier (L)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Anaëlle Dubois (A)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Alexia Paturel (A)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Nadim Fares (N)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Damien Cohen (D)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Phillippe Merle (P)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France; Department of Hepatology, Groupement Hospitalier Nord, Hospices Civils De Lyon, Lyon, 69000 France.

Joel Lachuer (J)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France; ProfileXpert, SFR-Est, CNRS UMR-S3453, INSERM US7, Lyon Cedex 08, F-69373, France.

Anne Wierinckx (A)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France; ProfileXpert, SFR-Est, CNRS UMR-S3453, INSERM US7, Lyon Cedex 08, F-69373, France.

Pierre Saintigny (P)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France; Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Brigitte Bancel (B)

Service d'Anatomopathologie, Groupement Hospitalier Est, Hospices Civils De Lyon, Lyon, 69000, France.

Janick Selves (J)

Anatomie Et Cytologie Pathologiques Pôle IUC Oncopole CHU Institut Universitaire Du Cancer De Toulouse - Oncopole, Toulouse, F- 31059, France.

Anne Schnitzler (A)

Department of Genetics, Institut Curie, PSL Research University, Paris, F-75005, France.

Bérengère Ouine (B)

Department of Translational Research, Institut Curie, PSL Research University, Paris, F-75005, France.

Aurélie Cartier (A)

Department of Translational Research, Institut Curie, PSL Research University, Paris, F-75005, France.

Leanne de Koning (L)

Department of Translational Research, Institut Curie, PSL Research University, Paris, F-75005, France.

Vincent Puard (V)

Department of Translational Research, Institut Curie, PSL Research University, Paris, F-75005, France.

Ivan Bieche (I)

Department of Genetics, Institut Curie, PSL Research University, Paris, F-75005, France.

Hector Hernandez-Vargas (H)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Janet Hall (J)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France.

Isabelle Chemin (I)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, CNRS, Centre Léon Bérard, Centre De Recherche En Cancérologie De Lyon, Lyon, 69008, France. Electronic address: Isabelle.chemin@inserm.fr.

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