The investigation of drug repurposing for HDAC1 inhibitory effects by in silico and in vitro methods
Year 2023,
, 287 - 293, 28.12.2023
Hüseyin İstanbullu
,
Ezgi Turunç
,
Sami Hamdoun
,
Merve Saylam
,
Halil Koyu
,
Tijen Kaya-temiz
Abstract
Background and Aims:Histone deacetylases (HDACs) modulate chromatin structure and regulate gene expression. The imbalance in chromatin acetylation and dysregulation of histone deacetylases are challenging in many pathologies, ranging from cancer to neurodegeneration. Computer-based in silico methods are becoming increasingly important in the determination of therapeutic targets and the development of personalized treatment approaches. This study aimed to investigate the HDAC1 inhibitory effects of chronic prescription drugs using in silico and in vitro methods.
Methods:Five chronically used prescription drugs were chosen: ipratropium bromide, metoprolol, leflunomide, nateglinide, and levothyroxine. Molecular docking was performed for each of the chosen drugs as well as the known inhibitor Trichostatin A on HDAC1. The binding pose with the best scores was saved for each compound and analyzed for its interaction with the protein. An HDAC1 inhibitor screening assay kit was used to determine the IC50 value for each drug.
Results:The IC50 values for HDAC1 inhibition by ipratropium bromide, metoprolol, leflunomide, nateglinide, and levothyroxine were found to be 352.10 μM, 255.70 μM, 219.80 μM, 289.50 μM, and 132.70 μM, respectively, whereas the value for the positive control Trichostatin A was 36.13 nM. GraphPad Prism 5 was used to conduct statistical analyses.
Conclusion:In this study, the in vitro HDAC1 inhibitory effect of ipratropium bromide, metoprolol, leflunomide, nateglinide, and levothyroxine is shown for the first time. In silico and in vitro methodologies used to show HDAC1 inhibitory activity in marketed drugs can provide insight into new drug discovery studies against cancer or neurodegenerative diseases.
Supporting Institution
Izmir Katip Celebi University Scientific Research Coordinatorship
Project Number
2018-ONAP-TIPF-0008
Thanks
The authors thank all study participants for their cooperation and the institutions for their support. The authors extend their appreciation to the Izmir Katip Celebi University Scientific Research Coordinatorship.
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Year 2023,
, 287 - 293, 28.12.2023
Hüseyin İstanbullu
,
Ezgi Turunç
,
Sami Hamdoun
,
Merve Saylam
,
Halil Koyu
,
Tijen Kaya-temiz
Project Number
2018-ONAP-TIPF-0008
References
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- Li, Y.Y., Jones, S. J. (2012). Drug repositioning for personalized medicine. Genome Medicine, 4(3):27. https://doi.org/10.1186/gm326 google scholar
- Lindemann, R. K., Gabrielli, B., Johnstone, R.W. (2004). Histone-deacetylase inhibitors for the treatment of cancer. Cell Cycle, 3(6):777-786. https://doi.org/10.4161/cc.3.6.927 google scholar
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- Park, H., Kim, S., Kim, Y.E., Lim, S.J. (2010). A structure-based virtual screening approach toward the discovery of histone deacetylase inhibitors: identification of promis-ing zinc-chelating groups. ChemMedChem., 5(4):591-597. https://doi.org/10.1002/cmdc.200900500 google scholar
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- Pushpakom, S., Iorio, F., Eyers, P.A., Escott, K.J., Hopper, S., Wells, A.... Pirmohamed, M. (2019). Drug repurposing: progress, challenges and recommendations. Nature Reviews Drug Discovery, 18(1):41-58. https://doi.org/10.1038/nrd.2018.168 google scholar
- Serebryannyy, L.A., Cruz, C.M., de Lanerolle, P. (2016). A Role for Nuclear Actin in HDAC 1 and 2 Regulation. Scientific Reports, 6:28460. https://doi.org/10.1038/srep28460 google scholar
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