Exploiting the potential of autophagy in cisplatin therapy: A new strategy to overcome resistance.

Resistance to cisplatin is a major challenge in the current cancer therapy. In order to explore new therapeutic strategies to cisplatin resistance, we evaluated, in a model of lung cancer (H1299 and H460 cell lines), the nature of the pathways leading to cell death. We observed that H1299 displayed...

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Detalles Bibliográficos
Autores: García Cano, Jesús, Ambroise, Gorbatchev, Pascual Serra, Raquel, Carrión Núñez de Arenas, María del Carmen, Serrano Oviedo, Leticia, Ortega Muelas, Marta, Cimas Felipe, Francisco José, Sabater, Sebastià, Ruiz Hidalgo, María José, Sánchez Pérez, Isabel, Mas López, Antonio, Jalón Sotes, Félix Ángel, Vázquez, Aimé, Sánchez Prieto, Ricardo
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Fundación Dialnet. Universidad de La Rioja
Repositorio:RUIdeRA. Repositorio Institucional de la UCLM
OAI Identifier:oai:ruidera.uclm.es:10578/47974
Acceso en línea:https://hdl.handle.net/10578/47974
Access Level:acceso abierto
Palabra clave:Apoptosis
Autophagy
Cisplatin
Monoplatin
Synthetic lethality
Descripción
Sumario:Resistance to cisplatin is a major challenge in the current cancer therapy. In order to explore new therapeutic strategies to cisplatin resistance, we evaluated, in a model of lung cancer (H1299 and H460 cell lines), the nature of the pathways leading to cell death. We observed that H1299 displayed a natural resistance to cisplatin due to an inability to trigger an apoptotic response that correlates with the induction of autophagy. However, pharmacological and genetic approaches showed how autophagy was a mechanism associated to cell death rather than to resistance. Indeed, pro-autophagic stimuli such as mTOR or Akt inhibition mediate cell death in both cell lines to a similar extent. We next evaluated the response to a novel platinum compound, monoplatin, able to promote cell death in an exclusive autophagy-dependent manner. In this case, no differences were observed between both cell lines. Furthermore, in response to monoplatin, two molecular hallmarks of cisplatin response (p53 and MAPKs) were not implicated, indicating the ability of this pro-autophagic compound to overcome cisplatin resistance. In summary, our data highlight how induction of autophagy could be used in cisplatin resistant tumours and an alternative treatment for p53 mutated patient in a synthetic lethally approach.