KRAS-regulated glutamine metabolism requires UCP2-mediated aspartate transport to support pancreatic cancer growth.
Animals
Aspartic Acid
/ metabolism
Biological Transport, Active
Carcinoma, Pancreatic Ductal
/ metabolism
Cell Line, Tumor
Cytosol
/ metabolism
Female
Glutamine
/ metabolism
Humans
Mice
Mice, SCID
Mitochondria
/ metabolism
NADP
/ metabolism
Oxidation-Reduction
Pancreatic Neoplasms
/ metabolism
Proto-Oncogene Proteins p21(ras)
/ metabolism
Reactive Oxygen Species
/ metabolism
Uncoupling Protein 2
/ metabolism
Xenograft Model Antitumor Assays
Journal
Nature metabolism
ISSN: 2522-5812
Titre abrégé: Nat Metab
Pays: Germany
ID NLM: 101736592
Informations de publication
Date de publication:
12 2020
12 2020
Historique:
received:
14
09
2019
accepted:
22
10
2020
pubmed:
25
11
2020
medline:
6
1
2021
entrez:
24
11
2020
Statut:
ppublish
Résumé
The oncogenic KRAS mutation has a critical role in the initiation of human pancreatic ductal adenocarcinoma (PDAC) since it rewires glutamine metabolism to increase reduced nicotinamide adenine dinucleotide phosphate (NADPH) production, balancing cellular redox homeostasis with macromolecular synthesis
Identifiants
pubmed: 33230296
doi: 10.1038/s42255-020-00315-1
pii: 10.1038/s42255-020-00315-1
doi:
Substances chimiques
KRAS protein, human
0
Reactive Oxygen Species
0
UCP2 protein, human
0
Uncoupling Protein 2
0
Glutamine
0RH81L854J
Aspartic Acid
30KYC7MIAI
NADP
53-59-8
Proto-Oncogene Proteins p21(ras)
EC 3.6.5.2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1373-1381Subventions
Organisme : Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research)
ID : IG 2014 Id.15404
Pays : International
Organisme : Ministero dell'Istruzione, dell'Università e della Ricerca (Ministry of Education, University and Research)
ID : 2017PAB8EM_002
Pays : International
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