HIF1α suppresses tumor cell proliferation through inhibition of aspartate biosynthesis

Cellular aspartate drives cancer cell proliferation, but signaling pathways that rewire aspartate biosynthesis to control cell growth remain largely unknown. Hypoxia-inducible factor-1α (HIF1α) can suppress tumor cell proliferation. Here, we discovered that HIF1α acts as a direct repressor of aspart...

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Detalhes bibliográficos
Autores: Meléndez-Rodríguez, Florinda, Urrutia, Andrés A., Lorendeau, Doriane, Rinaldi, Gianmarco, Roche, Olga, Böğürcü-Seidel, Nuray, Ortega Muelas, Marta, Mesa-Ciller, Claudia, Turiel, Guillermo, Bouthelier, Antonio, Hernansanz-Agustín, Pablo, Elorza, Ainara, Escasany, Elia, Yang Li, Qilong Oscar, Torres-Capelli, Mar, Tello, Daniel, Fuertes, Esther, Fraga, Enrique, Martínez-Ruiz, Antonio, Pérez González, María Belén, Giménez-Bachs, Jose Miguel, Salinas-Sánchez, Antonio S., Acker, Till, Sánchez Prieto, Ricardo, Fendt, Sarah Maria, De Bock, Katrien, Aragonés López, Julián
Formato: artículo
Fecha de publicación:2019
País:España
Recursos:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/688593
Acesso em linha:http://hdl.handle.net/10486/688593
https://dx.doi.org/10.1016/j.celrep.2019.01.106
Access Level:acceso abierto
Palavra-chave:Aspartate biosynthesis
Cancer
Glutamine
GOT1
GOT2
HIF1α
Oxygen
Proliferation
Renal cell carcinoma
Medicina
Descrição
Resumo:Cellular aspartate drives cancer cell proliferation, but signaling pathways that rewire aspartate biosynthesis to control cell growth remain largely unknown. Hypoxia-inducible factor-1α (HIF1α) can suppress tumor cell proliferation. Here, we discovered that HIF1α acts as a direct repressor of aspartate biosynthesis involving the suppression of several key aspartate-producing proteins, including cytosolic glutamic-oxaloacetic transaminase-1 (GOT1) and mitochondrial GOT2. Accordingly, HIF1α suppresses aspartate production from both glutamine oxidation as well as the glutamine reductive pathway. Strikingly, the addition of aspartate to the culture medium is sufficient to relieve HIF1α-dependent repression of tumor cell proliferation. Furthermore, these key aspartate-producing players are specifically repressed in VHL-deficient human renal carcinomas, a paradigmatic tumor type in which HIF1α acts as a tumor suppressor, highlighting the in vivo relevance of these findings. In conclusion, we show that HIF1α inhibits cytosolic and mitochondrial aspartate biosynthesis and that this mechanism is the molecular basis for HIF1α tumor suppressor activity. Meléndez-Rodríguez et al. show that HIF1α impairs oxidative and reductive aspartate biogenesis, which consequently drives HIF1α-dependent suppression of tumor cell proliferation. Mechanistically, HIF1α represses the aspartate-producing enzymes GOT1 and GOT2 in several biological settings, including human VHL-deficient renal cell carcinoma, in which HIF1α can act as a tumor suppressor

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