PUBLICATION
A Comprehensive Evaluation of Sdox, a Promising H2S-Releasing Doxorubicin for the Treatment of Chemoresistant Tumors
- Authors
- Alov, P., Al Sharif, M., Aluani, D., Chegaev, K., Dinic, J., Divac Rankov, A., Fernandes, M.X., Fusi, F., García-Sosa, A.T., Juvonen, R., Kondeva-Burdina, M., Padrón, J.M., Pajeva, I., Pencheva, T., Puerta, A., Raunio, H., Riganti, C., Tsakovska, I., Tzankova, V., Yordanov, Y., Saponara, S.
- ID
- ZDB-PUB-220325-2
- Date
- 2022
- Source
- Frontiers in pharmacology 13: 831791 (Journal)
- Registered Authors
- Divac Rankov, Aleksandra
- Keywords
- P-glycoprotein, cytochrome P450, doxorubicin, hERG, hepatotoxicity, in silico profiling, off-targets, zebrafish
- MeSH Terms
- none
- PubMed
- 35321325 Full text @ Front Pharmacol
Citation
Alov, P., Al Sharif, M., Aluani, D., Chegaev, K., Dinic, J., Divac Rankov, A., Fernandes, M.X., Fusi, F., García-Sosa, A.T., Juvonen, R., Kondeva-Burdina, M., Padrón, J.M., Pajeva, I., Pencheva, T., Puerta, A., Raunio, H., Riganti, C., Tsakovska, I., Tzankova, V., Yordanov, Y., Saponara, S. (2022) A Comprehensive Evaluation of Sdox, a Promising H2S-Releasing Doxorubicin for the Treatment of Chemoresistant Tumors. Frontiers in pharmacology. 13:831791.
Abstract
Sdox is a hydrogen sulfide (H2S)-releasing doxorubicin effective in P-glycoprotein-overexpressing/doxorubicin-resistant tumor models and not cytotoxic, as the parental drug, in H9c2 cardiomyocytes. The aim of this study was the assessment of Sdox drug-like features and its absorption, distribution, metabolism, and excretion (ADME)/toxicity properties, by a multi- and transdisciplinary in silico, in vitro, and in vivo approach. Doxorubicin was used as the reference compound. The in silico profiling suggested that Sdox possesses higher lipophilicity and lower solubility compared to doxorubicin, and the off-targets prediction revealed relevant differences between Dox and Sdox towards several cancer targets, suggesting different toxicological profiles. In vitro data showed that Sdox is a substrate with lower affinity for P-glycoprotein, less hepatotoxic, and causes less oxidative damage than doxorubicin. Both anthracyclines inhibited CYP3A4, but not hERG currents. Unlike doxorubicin, the percentage of zebrafish live embryos at 72 hpf was not affected by Sdox treatment. In conclusion, these findings demonstrate that Sdox displays a more favorable drug-like ADME/toxicity profile than doxorubicin, different selectivity towards cancer targets, along with a greater preclinical efficacy in resistant tumors. Therefore, Sdox represents a prototype of innovative anthracyclines, worthy of further investigations in clinical settings.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping