
International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113614 - 113614
Опубликована: Ноя. 15, 2024
Язык: Английский
International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113614 - 113614
Опубликована: Ноя. 15, 2024
Язык: Английский
Journal of Natural Products, Год журнала: 2025, Номер unknown
Опубликована: Янв. 11, 2025
A chemical investigation of the soil-derived fungus Trichocladium sp. XZ8 led to isolation five new indole alkaloids, trichindoles A–E (1–5), with diverse architectures, along seven known analogues (6–12). Their structures were elucidated by extensive spectroscopic data analysis, and their absolute configurations determined single-crystal X-ray diffraction modified Mosher's method. Compound 1 is a polyketide-alkaloid hybrid incorporating rare succinimide motif, compound 2 represents first example dimeric isopentenyl indole-containing alkaloid bridged propane-1,2-diol moiety. Compounds 1, 4, 8, 11, 12 showed significant neuroprotective effects against RSL3-induced ferroptosis in PC12 cells at 10 μM. Moreover, 4 might ameliorate through regulation SLC7A11 pathway ferritinophagy, suggesting potential as promising lead compounds for treatment neurodegenerative diseases.
Язык: Английский
Процитировано
0European Journal of Pharmacology, Год журнала: 2025, Номер unknown, С. 177746 - 177746
Опубликована: Май 1, 2025
Eukaryotic elongation factor 2 kinase (eEF2K), a calcium/calmodulin-dependent protein kinase, exhibits paradoxical activation and overexpression in numerous tumors, suggesting potential advantageous role for cancer cells. eEF2K phosphorylates inactivates its downstream target, eukaryotic (eEF2), thereby negatively regulating synthesis. Despite being translation inhibitor, inhibition alone has demonstrated limited anti-cancer efficacy. This study investigates novel approach to targeting therapy, exploring beyond established synthesis regulation. We found that pharmacological of using A484954 resulted minimal cytotoxicity but effectively reduced eEF2 phosphorylation. Surprisingly, impaired de novo induced mild oxidative stress across multiple cell lines. Furthermore, compromised cellular antioxidant defenses, leading enhanced ROS accumulation when challenged with stressors. Notably, potentiated ferroptosis induction lipid peroxidation combined inducers or glutathione depletion. These findings were corroborated by silencing, which similarly increased basal levels, sensitivity stress, promoted ferroptosis. Our results reveal previously unrecognized maintaining redox homeostasis suggest may be promising strategy sensitize cells ferroptosis-inducing therapies.
Язык: Английский
Процитировано
0International Immunopharmacology, Год журнала: 2024, Номер 143, С. 113614 - 113614
Опубликована: Ноя. 15, 2024
Язык: Английский
Процитировано
0