Metabolic reprogramming in cholangiocarcinoma.

CD36 IDH1/2 PGC1α cancer stem cells fatty acid synthase fatty acids glutamine glycolysis mTOR methionine adenosyltransferases mitochondria oxidative metabolism

Journal

Journal of hepatology
ISSN: 1600-0641
Titre abrégé: J Hepatol
Pays: Netherlands
ID NLM: 8503886

Informations de publication

Date de publication:
09 2022
Historique:
received: 28 02 2022
revised: 16 04 2022
accepted: 28 04 2022
pubmed: 21 5 2022
medline: 23 8 2022
entrez: 20 5 2022
Statut: ppublish

Résumé

Metabolic reprogramming is a hallmark of cancer and allows tumour cells to meet the increased energy demands required for rapid proliferation, invasion, and metastasis. Indeed, many tumour cells acquire distinctive metabolic and bioenergetic features that enable them to survive in resource-limited conditions, mainly by harnessing alternative nutrients. Several recent studies have explored the metabolic plasticity of cancer cells with the aim of identifying new druggable targets, while therapeutic strategies to limit the access to nutrients have been successfully applied to the treatment of some tumours. Cholangiocarcinoma (CCA), a highly heterogeneous tumour, is the second most common form of primary liver cancer. It is characterised by resistance to chemotherapy and poor prognosis, with 5-year survival rates of below 20%. Deregulation of metabolic pathways have been described during the onset and progression of CCA. Increased aerobic glycolysis and glutamine anaplerosis provide CCA cells with the ability to generate biosynthetic intermediates. Other metabolic alterations involving carbohydrates, amino acids and lipids have been shown to sustain cancer cell growth and dissemination. In this review, we discuss the complex metabolic rewiring that occurs during CCA development and leads to unique nutrient addiction. The possible role of therapeutic interventions based on metabolic changes is also thoroughly discussed.

Identifiants

pubmed: 35594992
pii: S0168-8278(22)00314-2
doi: 10.1016/j.jhep.2022.04.038
pii:
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

849-864

Informations de copyright

Copyright © 2022 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest Dr Braconi (or spouse) receives honoraria from Incyte, Roche, EliLilly, Merck-Serono. Dr. Marra receives or has received honoraria from AstraZeneca, Bayer, Ipsen, Merck/EISAI. Please refer to the accompanying ICMJE disclosure forms for further details.

Auteurs

Chiara Raggi (C)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy. Electronic address: chiara.raggi@unifi.it.

Maria Letizia Taddei (ML)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.

Colin Rae (C)

Institute of Cancer Sciences, The University of Glasgow, Glasgow, United Kingdom.

Chiara Braconi (C)

Institute of Cancer Sciences, The University of Glasgow, Glasgow, United Kingdom; Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.

Fabio Marra (F)

Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy. Electronic address: fabio.marra@unifi.it.

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Classifications MeSH