HeLa TI cell-based assay as a new approach to screen for chemicals able to reactivate the expression of epigenetically silenced genes

Chemicals reactivating epigenetically silenced genes target diverse classes of enzymes, including DNMTs, HDACs, HMTs and BET protein family members. They can strongly influence the expression of genes and endogenous retroviral elements with concomitant dsRNA synthesis and massive transcription of LTRs. Chemicals reactivating gene expression may cause both beneficial effects in cancer cells and may be hazardous by promoting carcinogenesis. Among chemicals used in medicine and commerce, only a small fraction has been studied with respect to their influence on epigenetic silencing. Screening of chemicals reactivating silent genes requires adequate systems mimicking whole-genome processes. We used a HeLa TSA-inducible cell population (HeLa TI cells) obtained by retroviral infection of a GFP-containing vector followed by several rounds of cell sorting for screening purposes. Previously, the details of GFP epigenetic silencing in HeLa TI cells were thoroughly described. Herein, we show that the epigenetically repressed gene GFP is reactivated by 15 agents, including HDAC inhibitors–vorinostat, sodium butyrate, valproic acid, depsipeptide, pomiferin, and entinostat; DNMT inhibitors–decitabine, 5-azacytidine, RG108; HMT inhibitors–UNC0638, BIX01294, DZNep; a chromatin remodeler–curaxin CBL0137; and BET inhibitors–JQ-1 and JQ-35. We demonstrate that combinations of epigenetic modulators caused a significant increase in cell number with reactivated GFP compared to the individual effects of each agent. HeLa TI cells are competent to metabolize xenobiotics and possess constitutively expressed and inducible cytochrome P450 mono-oxygenases involved in xenobiotic biotransformation. Thus, HeLa TI cells may be used as an adequate test system for the extensive screening of chemicals, including those that must be metabolically activated. Studying the additional metabolic activation of xenobiotics, we surprisingly found that the rat liver S9 fraction, which has been widely used for xenobiotic activation in genotoxicity tests, reactivated epigenetically silenced genes. Applying the HeLa TI system, we show that N-nitrosodiphenylamine and N-nitrosodimethylamine reactivate epigenetically silenced genes, probably by affecting DNA methylation. © 2021 Maksimova et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Maksimova V.1 , Shalginskikh N.1, 2 , Vlasova O.1 , Usalka O.1, 3 , Beizer A.1 , Bugaeva P.4 , Fedorov D.1, 5 , Lizogub O.1, 3 , Lesovaya E.1, 6 , Katz R.2 , Belitsky G. 1 , Kirsanov K. 1, 7 , Yakubovskaya M.1
Public Library of Science
Номер выпуска
6 June 2021
  • 1 Department of Chemical Carcinogenesis, Institute of Carcinogenesis, N.N. Blokhin National Medical Research Center of Oncology, Moscow, Russian Federation
  • 2 Fox Chase Cancer Center, Temple University, Philadelphia, PA, United States
  • 3 International School "Medicine of the Future", Sechenov University, Moscow, Russian Federation
  • 4 Department of Translational Neurobiology, Julius-Maximilians-Universität of Würzburg, Würzburg, Germany
  • 5 Department of Urology, A.V. Vishnevsky National Medical Research Center of Surgery, Moscow, Russian Federation
  • 6 Department of Oncology, Ryazan State Medical University, Ryazan, Russian Federation
  • 7 Department of General and Medical Practice, Medical Institute, Peoples’ Friendship University of Russia, Moscow, Russian Federation
Ключевые слова
2 cyclohexyl n (1 isopropyl 4 piperidinyl) 6 methoxy 7 [3 (1 pyrrolidinyl)propoxy] 4 quinazolinamine; 3 deazaneplanocin A; 4 (4 chlorophenyl) 2,3,9 trimethyl 6h thieno[3,2 f][1,2,4]triazolo[4,3 a][1,4]diazepine 6 acetic acid tert butyl ester; azacitidine; butyric acid; cytochrome P450; decitabine; depsipeptide; dimethylnitrosamine; diphenylnitrosamine; entinostat; histone deacetylase inhibitor; n (1 benzyl 4 piperidinyl) 2 (hexahydro 4 methyl 1h 1,4 diazepin 1 yl) 6,7 dimethoxy 4 quinazolinamine; n phthaloyltryptophan; pomiferin; tazemetostat; unclassified drug; unspecific monooxygenase; valproic acid; vorinostat; xenobiotic agent; animal tissue; Article; biotransformation; cell assay; cell count; cell selection; cell survival; controlled study; cytotoxicity; epigenetics; gene; gene expression; gene silencing; genotoxicity; GFP gene; HeLa cell line; HeLa trichostatin A inducible cell; human; human cell; metabolic activation; nonhuman; rat; retrovirus infection
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