» Articles » PMID: 30974899

Statins Do Not Directly Inhibit the Activity of Major Epigenetic Modifying Enzymes

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2019 Apr 13
PMID 30974899
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The potential anticancer effects of statins-a widely used class of cholesterol lowering drugs-has generated significant interest, as has the use of epigenetic modifying drugs such as HDAC and DNMT inhibitors. We set out to investigate the effect of statin drugs on epigenetic modifications in multiple cell lines, including hepatocellular carcinoma, breast carcinoma, leukemic macrophages, cervical adenocarcinoma, and insulin-secreting cells, as well as liver extracts from statin-treated C57B1/6J mice. Cells or cell extracts were treated with statins and with established epigenetic modulators, and HDAC, HAT, and DNMT activities were quantified. We also examined histone acetylation by immunoblotting. Statins altered neither HDAC nor HAT activity. Accordingly, acetylation of histones H3 and H4 was unchanged with statin treatment. However, statins tended to increase DNMT activity. These results indicate that direct inhibition of the major classes of epigenetic modifying enzymes, as previously reported elsewhere, is unlikely to contribute to any anticancer effects of statins. This study concerned global effects on epigenetic enzyme activities and histone acetylation; whether statins influence epigenetic modifications in certain genomic regions, cannot be ruled out and remains to be investigated.

Citing Articles

Gene regulatory network topology governs resistance and treatment escape in glioma stem-like cells.

Park J, Hothi P, de Lomana A, Pan M, Calder R, Turkarslan S Sci Adv. 2024; 10(23):eadj7706.

PMID: 38848360 PMC: 11160475. DOI: 10.1126/sciadv.adj7706.


Simvastatin-Mediated Nrf2 Activation Induces Fetal Hemoglobin and Antioxidant Enzyme Expression to Ameliorate the Phenotype of Sickle Cell Disease.

Xi C, Palani C, Takezaki M, Shi H, Horuzsko A, Pace B Antioxidants (Basel). 2024; 13(3).

PMID: 38539870 PMC: 10968127. DOI: 10.3390/antiox13030337.


Current Approaches to Epigenetic Therapy.

Griazeva E, Fedoseeva D, Radion E, Ershov P, Meshkov I, Semyanihina A Epigenomes. 2023; 7(4).

PMID: 37873808 PMC: 10594535. DOI: 10.3390/epigenomes7040023.


Unraveling the Anticancer Potential of Statins: Mechanisms and Clinical Significance.

Zaky M, Fan C, Zhang H, Sun X Cancers (Basel). 2023; 15(19).

PMID: 37835481 PMC: 10572000. DOI: 10.3390/cancers15194787.


Butyrate Lowers Cellular Cholesterol through HDAC Inhibition and Impaired SREBP-2 Signalling.

Bridgeman S, Woo H, Newsholme P, Mamotte C Int J Mol Sci. 2022; 23(24).

PMID: 36555149 PMC: 9779842. DOI: 10.3390/ijms232415506.


References
1.
Brueckner B, Garcia Boy R, Siedlecki P, Musch T, Kliem H, Zielenkiewicz P . Epigenetic reactivation of tumor suppressor genes by a novel small-molecule inhibitor of human DNA methyltransferases. Cancer Res. 2005; 65(14):6305-11. DOI: 10.1158/0008-5472.CAN-04-2957. View

2.
Lin Y, Lin J, Chou C, Chang Y, Yeh S, Chen C . Statins increase p21 through inhibition of histone deacetylase activity and release of promoter-associated HDAC1/2. Cancer Res. 2008; 68(7):2375-83. DOI: 10.1158/0008-5472.CAN-07-5807. View

3.
Codd R, Braich N, Liu J, Soe C, Pakchung A . Zn(II)-dependent histone deacetylase inhibitors: suberoylanilide hydroxamic acid and trichostatin A. Int J Biochem Cell Biol. 2008; 41(4):736-9. DOI: 10.1016/j.biocel.2008.05.026. View

4.
Liu Z, Xie Z, Jones W, Pavlovicz R, Liu S, Yu J . Curcumin is a potent DNA hypomethylation agent. Bioorg Med Chem Lett. 2008; 19(3):706-9. DOI: 10.1016/j.bmcl.2008.12.041. View

5.
Jove M, Serrano J, Bellmunt M, Cassanye A, Angles N, Reguant J . When cholesterol is not cholesterol: a note on the enzymatic determination of its concentration in model systems containing vegetable extracts. Lipids Health Dis. 2010; 9:65. PMC: 2901322. DOI: 10.1186/1476-511X-9-65. View