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TITLE:
BRAF activation by metabolic stress promotes glycolysis sensitizing NRASQ61-mutated melanomas to targeted therapy - imarina:9286900

URV's Author/s:Yanes Torrado, Óscar
Author, as appears in the article.:McGrail K; Granado-Martínez P; Esteve-Puig R; García-Ortega S; Ding Y; Sánchez-Redondo S; Ferrer B; Hernandez-Losa J; Canals F; Manzano A; Navarro-Sabaté A; Bartrons R; Yanes O; Pérez-Alea M; Muñoz-Couselo E; Garcia-Patos V; Recio JA
Author's mail:oscar.yanes@urv.cat
Author identifier:0000-0003-3695-7157
Journal publication year:2022
Publication Type:Journal Publications
APA:McGrail K; Granado-Martínez P; Esteve-Puig R; García-Ortega S; Ding Y; Sánchez-Redondo S; Ferrer B; Hernandez-Losa J; Canals F; Manzano A; Navarro-Sab (2022). BRAF activation by metabolic stress promotes glycolysis sensitizing NRASQ61-mutated melanomas to targeted therapy. Nature Communications, 13(1), 7113-7113. DOI: 10.1038/s41467-022-34907-0
Papper original source:Nature Communications. 13 (1): 7113-7113
Abstract:NRAS-mutated melanoma lacks a specific line of treatment. Metabolic reprogramming is considered a novel target to control cancer; however, NRAS-oncogene contribution to this cancer hallmark is mostly unknown. Here, we show that NRASQ61-mutated melanomas specific metabolic settings mediate cell sensitivity to sorafenib upon metabolic stress. Mechanistically, these cells are dependent on glucose metabolism, in which glucose deprivation promotes a switch from CRAF to BRAF signaling. This scenario contributes to cell survival and sustains glucose metabolism through BRAF-mediated phosphorylation of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase-2/3 (PFKFB2/PFKFB3). In turn, this favors the allosteric activation of phosphofructokinase-1 (PFK1), generating a feedback loop that couples glycolytic flux and the RAS signaling pathway. An in vivo treatment of NRASQ61 mutant melanomas, including patient-derived xenografts, with 2-deoxy-D-glucose (2-DG) and sorafenib effectively inhibits tumor growth. Thus, we provide evidence for NRAS-oncogene contributions to metabolic rewiring and a proof-of-principle for the treatment of NRASQ61-mutated melanoma combining metabolic stress (glycolysis inhibitors) and previously approved drugs, such as sorafenib.© 2022. The Author(s).
Article's DOI:10.1038/s41467-022-34907-0
Link to the original source:https://www.nature.com/articles/s41467-022-34907-0
Papper version:info:eu-repo/semantics/publishedVersion
licence for use:https://creativecommons.org/licenses/by/3.0/es/
Department:Enginyeria Electrònica, Elèctrica i Automàtica
Licence document URL:https://repositori.urv.cat/ca/proteccio-de-dades/
Thematic Areas:Zootecnia / recursos pesqueiros
Saúde coletiva
Química
Psicología
Planejamento urbano e regional / demografia
Physics and astronomy (miscellaneous)
Physics and astronomy (all)
Odontología
Nutrição
Multidisciplinary sciences
Multidisciplinary
Medicina veterinaria
Medicina iii
Medicina ii
Medicina i
Materiais
Matemática / probabilidade e estatística
Interdisciplinar
Geociências
General physics and astronomy
General medicine
General chemistry
General biochemistry,genetics and molecular biology
Farmacia
Engenharias iv
Educação física
Ciências biológicas iii
Ciências biológicas ii
Ciências biológicas i
Ciências ambientais
Ciências agrárias i
Ciência da computação
Chemistry (miscellaneous)
Chemistry (all)
Biotecnología
Biodiversidade
Biochemistry, genetics and molecular biology (miscellaneous)
Biochemistry, genetics and molecular biology (all)
Astronomia / física
Antropologia / arqueologia
Keywords:Mutant melanoma
tumors
survival
raf
phosphorylation
mutations
kinase
glucose
cancer
6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase
Entity:Universitat Rovira i Virgili
Record's date:2024-09-07
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