1. First-In-Class Thiosemicarbazone Metal Complexes Targeting the Sigma-2 Receptor (S2R) as an Innovative Strategy against Pancreatic Cancer.
- Author
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Barbanente A, Kopecka J, Vitone D, Niso M, Rizzi R, Cuocci C, Abatematteo FS, Mastropasqua F, Colabufo NA, Margiotta N, Arnesano F, Riganti C, and Abate C
- Subjects
- Humans, Cell Line, Tumor, Animals, Structure-Activity Relationship, Cell Proliferation drug effects, Mice, Receptors, sigma metabolism, Receptors, sigma antagonists & inhibitors, Pancreatic Neoplasms drug therapy, Pancreatic Neoplasms pathology, Pancreatic Neoplasms metabolism, Thiosemicarbazones pharmacology, Thiosemicarbazones chemistry, Thiosemicarbazones chemical synthesis, Antineoplastic Agents pharmacology, Antineoplastic Agents chemistry, Antineoplastic Agents chemical synthesis, Coordination Complexes pharmacology, Coordination Complexes chemistry, Coordination Complexes chemical synthesis, Coordination Complexes therapeutic use, Apoptosis drug effects
- Abstract
Pancreatic cancer, with its increasing incidence and lowest 5-year survival rate, is predicted to become the second leading cause of cancer deaths by 2030. Current clinical trials have shown limited improvement, highlighting the need for new therapies. The sigma-2 receptor (S2R), with roles in tumor progression, is a target for novel thiosemicarbazones (TSCs). FA4 has shown potent activity against pancreatic cancer in vivo . We synthesized complexes of FA4 with Cu(II) and Pt(II), and compared their efficacy with complexes of the non-S2R-targeting TSC 1 . TSC-Cu exhibited over 50-fold higher in vitro cytotoxicity than TSCs-Pt, which was less active than TSCs. FA4 -Cu induced apoptotic cell death via ER and mitochondrial stress showing more potent activity than FA4 . This in vitro effect was replicated in the preclinical PANC-1 model, where FA4 -Cu was more potent than FA4 , 1 , and 1 -Cu. These results support further exploration of FA4 -Cu as a potential therapy for pancreatic cancer.
- Published
- 2024
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