Transposon delivery for CRISPR-based loss-of-function screen in mice identifies NF2 as a cooperating gene involved with the canonical WNT signaling molecular class of hepatocellular carcinoma.

CRISPR/Cas9 CTNNB1 Hepatocellular carcinoma NF2 Transposable elements

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 06 07 2023
revised: 25 07 2023
accepted: 27 07 2023
medline: 14 8 2023
pubmed: 14 8 2023
entrez: 14 8 2023
Statut: epublish

Résumé

Various molecular subclasses of hepatocellular carcinoma (HCC) exists, with many novel cooperating oncogenes and tumor suppressor genes involved in its tumorigenesis. The emerging importance of WNT signaling in HCC has been established. However, the intricate genetic mechanisms involved in this complex signaling pathway remains to be elucidated. Importantly, while some cooperating genes have been identified, there are still many unknown genes associated with catenin beta 1 (

Identifiants

pubmed: 37576222
doi: 10.1016/j.heliyon.2023.e18774
pii: S2405-8440(23)05982-0
pmc: PMC10412851
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e18774

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper

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Auteurs

Vincent W Keng (VW)

The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
Department of Applied Biology and Chemical Technology, State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University, Kowloon, Hong Kong, China.

Amy P Chiu (AP)

Department of Applied Biology and Chemical Technology, State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University, Kowloon, Hong Kong, China.

Jeffrey C To (JC)

The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
Department of Applied Biology and Chemical Technology, State Key Laboratory of Chemical Biology and Drug Discovery, The Hong Kong Polytechnic University, Kowloon, Hong Kong, China.

Xiao-Xiao Li (XX)

The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.

Michael A Linden (MA)

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA.

Khalid Amin (K)

Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA.

Branden S Moriarity (BS)

Masonic Cancer Center, Department of Pediatrics, and Center for Genome Engineering, University of Minnesota, Minneapolis, MN 55455, USA.

Kosuke Yusa (K)

Stem Cell Genetics, Institute for Life and Medical Sciences, Kyoto University, Kyoto, Japan.
Wellcome Sanger Institute, Cambridge CB10 1SA, UK.

Classifications MeSH