Urska Kamensek

Nanoformulation of a Pin1 inhibitor potentiates the efficacy of liposomal doxorubicin in second-line therapy for ovarian cancer

The second-line therapy for high-grade serous ovarian cancer (HGSOC) patients is generally ineffective. Drug selection is not aimed at improving overall survival, but rather based on residual toxicities, clinical judgment, and patient adherence. Therefore, the identification of more effective and targeted therapeutic strategies is critically needed. The Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (PIN1) has emerged as a key hallmark of cancer progression and represents a promising therapeutic target in ovarian cancer (OC). VS10, a novel PIN1 inhibitor developed by our group, has shown potent activity against ovarian cancer cell lines. In this study, a drug delivery system for VS10 was developed by formulating the inhibitor into nanocrystals stabilized with human serum albumin. Comprehensive physicochemical characterization of the formulation was performed using spectrophotometric quantification, dynamic light scattering (DLS) with zeta potential analysis, transmission electron microscopy (TEM), X-ray diffraction (XRD), fourier-transform infrared spectroscopy (FT-IR), and nuclear magnetic resonance (NMR). The nanocrystals exhibited favorable sustained release kinetics, as confirmed by in vitro release tests. The anticancer activity was further validated through IC

A carrier free delivery system of a MAGL inhibitor is effective on ovarian cancer

Monoacylglycerol lipase (MAGL) is a promising target for cancer therapy due to its involvement in lipid metabolism and its impact on cancer hallmarks like cell proliferation, migration, and tumor progression. A potent reversible MAGL inhibitor, MAGL23, has been recently developed by our group, demonstrating promising anticancer activities. To enhance its pharmacological properties, a nanoformulation using nanocrystals coated with albumin was prepared (MAGL23AF). In a previous work, the formulated inhibitor showed potency in ovarian and colon cancer cell lines in terms of IC