5-Azacytidine upregulates melatonin MT1 receptor expression in rat C6 glioma cells: oncostatic implications
Author:
Funder
Natural Sciences and Engineering Research Council of Canada.
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11033-020-05482-8.pdf
Reference35 articles.
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2. Liu J, Clough SJ, Hutchinson AJ et al (2015) MT1 and MT2 melatonin receptors: a therapeutic perspective. Annu Rev Pharmacol Toxicol 56:361–383. https://doi.org/10.1146/annurev-pharmtox-010814-124742
3. Galano A, Tan DX, Reiter RJ (2018) Melatonin: a versatile protector against oxidative DNA damage. Molecules 23:530
4. Phiel CJ, Zhang F, Huang EY et al (2001) Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem 276:36734–36741. https://doi.org/10.1074/jbc.M101287200
5. Castro LM, Gallant M, Niles LP (2005) Novel targets for valproic acid: up-regulation of melatonin receptors and neurotrophic factors in C6 glioma cells. J Neurochem 95:1227–1236. https://doi.org/10.1111/j.1471-4159.2005.03457.x
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