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Metabolic shift underlies tumor progression and immune evasion in S-nitrosoglutathione reductase-deficient cancer.
Mena-Osuna, Rafael; Mantrana, Ana; Guil-Luna, Silvia; Sánchez-Montero, María Teresa; Navarrete-Sirvent, Carmen; Morales-Ruiz, Teresa; Rivas-Crespo, Aurora; Toledano-Fonseca, Marta; García-Ortíz, María Victoria; García-Jurado, Gema; Gómez-España, María Auxiliadora; González-Fernández, Rafael; Villar, Carlos; Medina-Fernández, Francisco Javier; Villalba, José Manuel; Aranda, Enrique; Rodríguez-Ariza, Antonio.
Afiliación
  • Mena-Osuna R; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Mantrana A; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Guil-Luna S; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Sánchez-Montero MT; Cancer Network Biomedical Research Centre (CIBERONC), Madrid, Spain.
  • Navarrete-Sirvent C; Department of Medicine, Faculty of Medicine, University of Córdoba, Córdoba, Spain.
  • Morales-Ruiz T; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Rivas-Crespo A; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Toledano-Fonseca M; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • García-Ortíz MV; Department of Genetics, University of Córdoba, Córdoba, Spain.
  • García-Jurado G; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Gómez-España MA; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • González-Fernández R; Cancer Network Biomedical Research Centre (CIBERONC), Madrid, Spain.
  • Villar C; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Medina-Fernández FJ; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
  • Villalba JM; Department of Medicine, Faculty of Medicine, University of Córdoba, Córdoba, Spain.
  • Aranda E; Medical Oncology Department, Reina Sofía University Hospital, Córdoba, Spain.
  • Rodríguez-Ariza A; Maimonides Biomedical Research Institute of Córdoba (IMIBIC), Córdoba, Spain.
J Pathol ; 260(3): 261-275, 2023 07.
Article en En | MEDLINE | ID: mdl-37017456
S-nitrosoglutathione reductase (GSNOR) is a denitrosylase enzyme that has been suggested to play a tumor suppressor role, although the mechanisms responsible are still largely unclear. In this study, we show that GSNOR deficiency in tumors is associated with poor prognostic histopathological features and poor survival in patients with colorectal cancer (CRC). GSNOR-low tumors were characterized by an immunosuppressive microenvironment with exclusion of cytotoxic CD8+ T cells. Notably, GSNOR-low tumors exhibited an immune evasive proteomic signature along with an altered energy metabolism characterized by impaired oxidative phosphorylation (OXPHOS) and energetic dependence on glycolytic activity. CRISPR-Cas9-mediated generation of GSNOR gene knockout (KO) CRC cells confirmed in vitro and in vivo that GSNOR-deficiency conferred higher tumorigenic and tumor-initiating capacities. Moreover, GSNOR-KO cells possessed enhanced immune evasive properties and resistance to immunotherapy, as revealed following xenografting them into humanized mouse models. Importantly, GSNOR-KO cells were characterized by a metabolic shift from OXPHOS to glycolysis to produce energy, as indicated by increased lactate secretion, higher sensitivity to 2-deoxyglucose (2DG), and a fragmented mitochondrial network. Real-time metabolic analysis revealed that GSNOR-KO cells operated close to their maximal glycolytic rate, as a compensation for lower OXPHOS levels, explaining their higher sensitivity to 2DG. Remarkably, this higher susceptibility to glycolysis inhibition with 2DG was validated in patient-derived xenografts and organoids from clinical GSNOR-low tumors. In conclusion, our data support the idea that metabolic reprogramming induced by GSNOR deficiency is an important mechanism for tumor progression and immune evasion in CRC and that the metabolic vulnerabilities associated with the deficiency of this denitrosylase can be exploited therapeutically. © 2023 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidorreductasas / Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Pathol Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxidorreductasas / Neoplasias Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: J Pathol Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Reino Unido