Induction of autophagy-dependent ferroptosis to eliminate drug-tolerant human retinoblastoma cells.
Ontology highlight
ABSTRACT: Carboplatin is the most used first-line drug for the treatment of human retinoblastoma (RB), a rare form of cancer in infancy and childhood. However, the clinical application of carboplatin is restricted due to the emergence of acquired multi-drug resistance (MDR) after long-term treatment. Here, we report a new strategy to eliminate MDR RB cells by inducing autophagy-dependent ferroptosis. Compared with parent cells, carboplatin-resistant human RB cells have higher autophagy activity, which drives the formation of MDR to other chemotherapeutic drugs (e.g., etoposide and vincristine). In addition to confirming the traditional strategy of inhibiting autophagy to overcome MDR, we also establish an approach of inducing selective ferritinophagy to eliminate drug-resistant cells. We evaluate th
SUBMITTER: Liu K
PROVIDER: S-EPMC9163041 | biostudies-literature | 2022 Jun
REPOSITORIES: biostudies-literature
ACCESS DATA