| المساهمون: |
Carbone D., Vestuto V., Ferraro M.R., Ciaglia T., Pecoraro C., Sommella E., Cascioferro S., Salviati E., Novi S., Tecce M.F., Amodio G., Iraci N., Cirrincione G., Campiglia P., Diana P., Bertamino A., Parrino B., Ostacolo C., Carbone, Daniela, Vestuto, Vincenzo, Ferraro, Maria Rosalia, Ciaglia, Tania, Pecoraro, Camilla, Sommella, Eduardo, Cascioferro, Stella, Salviati, Emanuela, Novi, Sara, Tecce, Mario Felice, Amodio, Giuseppina, Iraci, Nunzio, Cirrincione, Girolamo, Campiglia, Pietro, Diana, Patrizia, Bertamino, Alessia, Parrino, Barbara, Ostacolo, Carmine |
| الوصف: |
The enzyme glutaminase-1 (GLS-1) has shown a clear and coherent implication in the progression and exacerbation of different aggressive tumors such as glioblastoma, hepatocarcinoma, pancreas, bone, and triple-negative breast cancer. Few chemotypes are currently available as selective GLS-1 inhibitors, and still, fewer of them are at the clinical stage. In the present paper, starting from a naturally-inspired antitumor compound library, metabolomics has been used to putatively identify the molecular mechanism underlying biological activity. GLS-1 was identified as a potential target. Biochemical analysis confirmed the hypothesis leading to the identification of a new hit compound acting as a GLS-1 selective inhibitor (IC50 = 3.96 ± 1.05 μM), compared to the GLS-2 isoform (IC50 = 12.90 ± 0.87 μM), with remarkable antitumor potency over different aggressive tumor cell lines. Molecular modelling studies revealed new insight into the drug-target interaction providing robust SAR clues for the rational hit-to-lead development. The approach undertaken underlines the wide potential of metabolomics applied to drug discovery, particularly in target identification and hit discovery following phenotype screening. |
