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Metabolic fate of the natural anticancer agent cucurbitacin B: an LC-MS/MS-enabled profiling of its major phase I and II conjugates in vivo.
- Source :
-
Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2024 Dec; Vol. 416 (29), pp. 7043-7062. Date of Electronic Publication: 2024 Oct 23. - Publication Year :
- 2024
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Abstract
- Cucurbitacin B (CuB) is a natural triterpenoid with diverse pharmacological effects including potent anticancer activity. However, its oral bioavailability is hampered by limited metabolism in vivo. We characterized CuB's in vivo metabolism in rats to uncover bioactive metabolites retaining therapeutic potential, using a robust UHPLC-Q-TOF-MS/MS workflow. This workflow combined molecular networking, fragmentation filtering, and mass defect filtering to identify CuB metabolites in rat urine, plasma, and feces following oral administration. Thirteen metabolites were identified and seven were confirmed. Major phase I transformations involved hydrolysis, reduction, epoxidation, and amination. Phase II conjugation included cysteine, glutathione, glucuronide, and gluconic acid conjugates. Notably, one of the main metabolites formed was the cysteine conjugate CuB-Cys. CuB-Cys maintained similar in vitro antiproliferative activity to CuB on HepG2, MCF-7, and PANC-1 cancer cell lines. However, it demonstrated lower cytotoxicity towards non-cancerous L02 cells, highlighting improved therapeutic selectivity. Mechanistically, CuB-Cys induced greater apoptotic signaling in HepG2 cells than CuB via enhanced caspase activation and disrupted BAX-Bcl-2 balance. This represents the first systematic characterization of CuB's in vivo metabolic pathway. The identification and confirmation of CuB-Cys provide insight for drug development efforts aiming to maintain therapeutic efficacy while reducing toxicity, via metabolite-based approaches. Our findings shed light on strategies for improving CuB's clinical potential.<br />Competing Interests: Declarations. Ethics approval: All animal handling and experimental procedures complied with the National Institutes of Health (NIH). Source of biological material: Male Sprague–Dawley rats (200 ± 20 g) were acquired from the Qing-Long-Shan Animal Breeding Farm (Nanjing, China, Certificate No. SX1207). Statement on animal welfare: All animal handling and experimental procedures were approved by the Animal Care and Use Committee of Nanjing University of Science and Technology. Conflict of interest: The authors declare no competing interests.<br /> (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.)
- Subjects :
- Animals
Humans
Rats
Male
Chromatography, High Pressure Liquid methods
Rats, Sprague-Dawley
Cell Line, Tumor
Apoptosis drug effects
Cell Proliferation drug effects
Liquid Chromatography-Mass Spectrometry
Triterpenes metabolism
Triterpenes pharmacokinetics
Triterpenes chemistry
Tandem Mass Spectrometry methods
Antineoplastic Agents pharmacokinetics
Antineoplastic Agents pharmacology
Antineoplastic Agents metabolism
Antineoplastic Agents chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1618-2650
- Volume :
- 416
- Issue :
- 29
- Database :
- MEDLINE
- Journal :
- Analytical and bioanalytical chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 39441433
- Full Text :
- https://doi.org/10.1007/s00216-024-05608-y