Detalle Publicación

ARTÍCULO
Inhibition of a G9a/DNMT network triggers immune-mediated bladder cancer regression
Autores: Segovia, C.; San José Enériz, Edurne; Munera-Maravilla, E.; Martinez-Fernandez, M.; Garate Iturriagagoitia, Leire; Miranda, E. ; Vilas Zornoza, Amaia; Lodewijk, I.; Rubio, C.; Segrelles, C. ; Valcarcel, L. V.; Rabal, O.; Casares Lagar, Noelia; Bernardini, A.; Suarez-Cabrera, C.; Lopez-Calderon, F. F.; Fortes Alonso, María Purificación; Casado, J. A. ; Duenas, M.; Villacampa Aubá, Felipe; Lasarte Sagastibelza, Juan José; Guerrero-Ramos, F.; de Velasco, G. ; Oyarzabal, J. ; Castellano, D.; Aguirre Ena, Xabier (Autor de correspondencia); Prosper Cardoso, Felipe (Autor de correspondencia); Paramio, J. M. (Autor de correspondencia)
Título de la revista: NATURE MEDICINE
ISSN: 1078-8956
Volumen: 25
Número: 7
Páginas: 1073 - 1081
Fecha de publicación: 2019
Lugar: WOS
Resumen:
Bladder cancer is lethal in its advanced, muscle-invasive phase with very limited therapeutic advances(1,2). Recent molecular characterization has defined new (epi) genetic drivers and potential targets for bladder cancer(3,4). The immune checkpoint inhibitors have shown remarkable efficacy but only in a limited fraction of bladder cancer patients(5-8). Here, we show that high G9a (EHMT2) expression is associated with poor clinical outcome in bladder cancer and that targeting G9a/DNMT methyltransferase activity with a novel inhibitor (CM-272) induces apoptosis and immunogenic cell death. Using an immunocompetent quadruple-knockout (Pten(loxP/loxP); Trp53(loxP/loxP); Rb1(loxP/loxP); Rbl1(-/-)) transgenic mouse model of aggressive metastatic, muscle-invasive bladder cancer, we demonstrate that CM-272 + cisplatin treatment results in statistically significant regression of established tumors and metastases. The antitumor effect is significantly improved when CM-272 is combined with anti-programmed cell death ligand 1, even in the absence of cisplatin. These effects are associated with an endogenous antitumor immune response and immunogenic cell death with the conversion of a cold immune tumor into a hot tumor. Finally, increased G9a expression was associated with resistance to programmed cell death protein 1 inhibition in a cohort of patients with bladder cancer. In summary, these findings support new and promising opportunities for the treatment of bladder cancer using a combination of epigenetic inhibitors and immune checkpoint blockade.