Glyphosate affects methylation in the promoter regions of selected tumor suppressors as well as expression of major cell cycle and apoptosis drivers in PBMCs (in vitro study).


Journal

Toxicology in vitro : an international journal published in association with BIBRA
ISSN: 1879-3177
Titre abrégé: Toxicol In Vitro
Pays: England
ID NLM: 8712158

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 21 10 2019
revised: 08 11 2019
accepted: 17 11 2019
pubmed: 22 11 2019
medline: 29 9 2020
entrez: 22 11 2019
Statut: ppublish

Résumé

We have determined the effect of glyphosate on selected epigenetic parameters and major cell cycle drivers in human peripheral blood mononuclear cells (PBMCs). The cells were incubated with glyphosate at 0.5, 10 and 100 μM. The analysis included: global DNA methylation, methylation in the promoter regions of tumor suppressor genes (P16, P21, TP53) and proto-oncogenes (BCL2, CCND1) by the Real-Time PCR and the expression profile of the indicated genes by Real-Time PCR. The obtained results have revealed significant reduction of global DNA methylation level in PBMCs exposed to glyphosate. Tested compound changed methylation pattern of the P21 and TP53 suppressor gene promoters, but in case of other analyzed genes: P16, BCL2 and CCND1 we did not identify any statistically significant changes. Gene profiling showed that glyphosate changed the expression of genes involved in the regulation of cell cycle and apoptosis. Glyphosate decreased expression of P16 and TP53 as well as an increase in the expression of BCl2, CCND1 and P21. Summing up, our results have shown a potential disturbance in methylation processes and gene expression in human PBMCs exposed to glyphosate, but the observed changes do not prejudge about the final metabolic effects, which are depended on many other factors.

Identifiants

pubmed: 31751608
pii: S0887-2333(19)30796-9
doi: 10.1016/j.tiv.2019.104736
pii:
doi:

Substances chimiques

Cell Cycle Proteins 0
Herbicides 0
Proto-Oncogene Proteins 0
Tumor Suppressor Proteins 0
Glycine TE7660XO1C

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104736

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Ewelina Woźniak (E)

University of Lodz, Faculty of Biology and Environmental Protection, Department of Biophysics of Environmental Pollution, Pomorska Str. 141/143, 90-236 Lodz, Poland; Medical University of Lodz, Department of Internal Diseases and Clinical Pharmacology, Laboratory of Tissue Immunopharmacology, Kniaziewicza Str. 1/5, 91-347 Lodz, Poland. Electronic address: ewelina.wozniak@umed.lodz.pl.

Edyta Reszka (E)

Department of Molecular Genetics and Epigenetics, Nofer Institute of Occupational Medicine, Teresy Str. 8, 91-348 Lodz, Poland.

Ewa Jabłońska (E)

Department of Molecular Genetics and Epigenetics, Nofer Institute of Occupational Medicine, Teresy Str. 8, 91-348 Lodz, Poland.

Aneta Balcerczyk (A)

University of Lodz, Faculty of Biology and Environmental Protection, Department of Molecular Biophysics, Pomorska Str. 141/143, 90-236 Lodz, Poland.

Marlena Broncel (M)

Medical University of Lodz, Department of Internal Diseases and Clinical Pharmacology, Laboratory of Tissue Immunopharmacology, Kniaziewicza Str. 1/5, 91-347 Lodz, Poland.

Bożena Bukowska (B)

University of Lodz, Faculty of Biology and Environmental Protection, Department of Biophysics of Environmental Pollution, Pomorska Str. 141/143, 90-236 Lodz, Poland.

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Classifications MeSH