Targeting ganglioneuromas with mTOR inhibitors.

AKT Ganglioneuroma mTOR inhibitor zebrafish model

Journal

Molecular & cellular oncology
ISSN: 2372-3556
Titre abrégé: Mol Cell Oncol
Pays: United States
ID NLM: 101642411

Informations de publication

Date de publication:
10 Jan 2021
Historique:
entrez: 8 2 2021
pubmed: 9 2 2021
medline: 9 2 2021
Statut: epublish

Résumé

We recently identified activated protein kinase B (PKB/AKT) as a tumorigenic driver in childhood ganglioneuroma. Inhibition of the mechanistic target of rapamycin (mTOR), a serine/threonine kinase downstream of AKT, effectively reduced the tumor burden in zebrafish with ganglioneuroma. We propose a clinical trial of mTOR inhibitors as a means to shrink large ganglioneuromas prior to surgical resection.

Identifiants

pubmed: 33553609
doi: 10.1080/23723556.2020.1856621
pii: 1856621
pmc: PMC7849689
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1856621

Subventions

Organisme : NCI NIH HHS
ID : K08 CA245251
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA210064
Pays : United States

Informations de copyright

© 2020 The Author(s). Published with license by Taylor & Francis Group, LLC.

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Auteurs

Ting Tao (T)

Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou, China.
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Hui Shi (H)

Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
College of Animal Sciences, Zhejiang University, Hangzhou, China.

Adam D Durbin (AD)

Division of Molecular Oncology, Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, USA.

A Thomas Look (AT)

Department of Pediatric Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Classifications MeSH