Wnt/β-Catenin-Pathway Alterations and Homologous Recombination Deficiency in Cholangiocarcinoma Cell Lines and Clinical Samples: Towards Specific Vulnerabilities.

APC HRD Olaparib PARP WNT cholangiocarcinoma intraductal papillary neoplasm of the bile duct β-catenin

Journal

Journal of personalized medicine
ISSN: 2075-4426
Titre abrégé: J Pers Med
Pays: Switzerland
ID NLM: 101602269

Informations de publication

Date de publication:
01 Aug 2022
Historique:
received: 17 06 2022
revised: 20 07 2022
accepted: 29 07 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 27 8 2022
Statut: epublish

Résumé

Cholangiocarcinoma (CCA) features a dismal prognosis with limited treatment options. Genomic studies have unveiled several promising targets in this disease, including fibroblast growth factor receptor (FGFR) fusions and isocitrate dehydrogenase (IDH) mutations. To fully harness the potential of genomically informed therapies in CCA, it is necessary to thoroughly characterize the available model organisms, including cell lines. One parameter to investigate in CCA is homologous recombination deficiency (HRD). While mutations in homologous recombinational repair (HRR)-related genes have been detected, their predictive value remains undetermined. Using a targeted next-generation sequencing approach, we analyzed 12 human CCA cell lines and compared them to 62 CCA samples of the molecular tumor board cohort. The AmoyDx

Identifiants

pubmed: 36013219
pii: jpm12081270
doi: 10.3390/jpm12081270
pmc: PMC9410222
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Alexander Scheiter (A)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.
Bavarian Center for Cancer Research/BZKF, 91054 Bavaria, Germany.

Frederik Hierl (F)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Ingrid Winkel (I)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Felix Keil (F)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Margit Klier-Richter (M)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Cédric Coulouarn (C)

INSERM, Université de Rennes, F-35042 Rennes, France.

Florian Lüke (F)

Bavarian Center for Cancer Research/BZKF, 91054 Bavaria, Germany.
Department of Internal Medicine III, University Hospital Regensburg, Hematology and Oncology, 93053 Regensburg, Germany.
Division of Personalized Tumor Therapy, Fraunhofer Institute for Toxicology and Experimental Medicine, 93053 Regensburg, Germany.

Arne Kandulski (A)

Department of Internal Medicine I, University Hospital Regensburg, 93053 Regensburg, Germany.

Matthias Evert (M)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Wolfgang Dietmaier (W)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Diego F Calvisi (DF)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Kirsten Utpatel (K)

Institute of Pathology, University of Regensburg, 93053 Regensburg, Germany.

Classifications MeSH