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
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
849-864Informations 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.