MCJ is a mitochondrial Tim23-related co-chaperonin known for its role in regulating oxidative phosphorylation efficiency, oxidative stress response and lipid metabolism. Recently, it has been proposed that the loss of MCJ correlates with cisplatin (CDDP)-resistance onset in ovarian cancer (OC), suggesting this protein as a potential prognostic factor during OC progression. However, the molecular mechanisms through which MCJ contributes to CDDP response remains poorly investigated. The present dataset collect data regarding the association between MCJ levels and accumulation of lipid droplets, tumorigenic features and sensitivity to CDDP in OC cells. Moreover, this dataset provides information on lipid peroxidation and ferroptosis induction in cells overexpressing MCJ, in presence or absence of Ferrostatin 1.
Stefano Miglietta, Manuela Sollazzo, Iacopo Gherardi, Sara Milioni, Beatrice Cavina, Lorena Marchio, et al. (2024). Mitochondrial Chaperonin MCJ Promotes Vulnerability to Ferroptosis of Chemoresistant Ovarian Cancer Cells – Dataset [10.6092/unibo/amsacta/7730].
Mitochondrial Chaperonin MCJ Promotes Vulnerability to Ferroptosis of Chemoresistant Ovarian Cancer Cells – Dataset
Stefano MigliettaCo-primo
Investigation
;Manuela SollazzoCo-primo
Investigation
;Iacopo GherardiInvestigation
;Sara MilioniInvestigation
;Beatrice CavinaInvestigation
;Lorena MarchioInvestigation
;Monica De LuiseInvestigation
;Camelia Alexandra CoadaSoftware
;Anna Myriam PerroneResources
;Ivana KurelacMethodology
;Giuseppe GasparreConceptualization
;Luisa IommariniConceptualization
;Anna Maria Ghelli
Conceptualization
;Anna Maria PorcelliUltimo
Supervision
2024
Abstract
MCJ is a mitochondrial Tim23-related co-chaperonin known for its role in regulating oxidative phosphorylation efficiency, oxidative stress response and lipid metabolism. Recently, it has been proposed that the loss of MCJ correlates with cisplatin (CDDP)-resistance onset in ovarian cancer (OC), suggesting this protein as a potential prognostic factor during OC progression. However, the molecular mechanisms through which MCJ contributes to CDDP response remains poorly investigated. The present dataset collect data regarding the association between MCJ levels and accumulation of lipid droplets, tumorigenic features and sensitivity to CDDP in OC cells. Moreover, this dataset provides information on lipid peroxidation and ferroptosis induction in cells overexpressing MCJ, in presence or absence of Ferrostatin 1.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.