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Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro
The evidence supporting the biological plausibility of the association of permethrin and malathion with hematological cancer is limited and contradictory; thus, further studies are needed. This study aimed to investigate whether in vitro exposure to 0.1 μM permethrin and malathion at 0, 24, 48 and 7...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094043/ https://www.ncbi.nlm.nih.gov/pubmed/37047231 http://dx.doi.org/10.3390/ijms24076259 |
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author | Navarrete-Meneses, María del Pilar Salas-Labadía, Consuelo Juárez-Velázquez, María del Rocío Moreno-Lorenzana, Dafné Gómez-Chávez, Fernando Olaya-Vargas, Alberto Pérez-Vera, Patricia |
author_facet | Navarrete-Meneses, María del Pilar Salas-Labadía, Consuelo Juárez-Velázquez, María del Rocío Moreno-Lorenzana, Dafné Gómez-Chávez, Fernando Olaya-Vargas, Alberto Pérez-Vera, Patricia |
author_sort | Navarrete-Meneses, María del Pilar |
collection | PubMed |
description | The evidence supporting the biological plausibility of the association of permethrin and malathion with hematological cancer is limited and contradictory; thus, further studies are needed. This study aimed to investigate whether in vitro exposure to 0.1 μM permethrin and malathion at 0, 24, 48 and 72 h after cell culture initiation induced changes in the gene expression and DNA methylation in mononuclear cells from bone marrow and peripheral blood (BMMCs, PBMCs). Both pesticides induced several gene expression modifications in both tissues. Through gene ontology analysis, we found that permethrin deregulates ion channels in PBMCs and BMMCs and that malathion alters genes coding proteins with nucleic acid binding capacity, which was also observed in PBMCs exposed to permethrin. Additionally, we found that both insecticides deregulate genes coding proteins with chemotaxis functions, ion channels, and cytokines. Several genes deregulated in this study are potentially associated with cancer onset and development, and some of them have been reported to be deregulated in hematological cancer. We found that permethrin does not induce DNA hypermethylation but can induce hypomethylation, and that malathion generated both types of events. Our results suggest that these pesticides have the potential to modify gene expression through changes in promoter DNA methylation and potentially through other mechanisms that should be investigated. |
format | Online Article Text |
id | pubmed-10094043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100940432023-04-13 Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro Navarrete-Meneses, María del Pilar Salas-Labadía, Consuelo Juárez-Velázquez, María del Rocío Moreno-Lorenzana, Dafné Gómez-Chávez, Fernando Olaya-Vargas, Alberto Pérez-Vera, Patricia Int J Mol Sci Article The evidence supporting the biological plausibility of the association of permethrin and malathion with hematological cancer is limited and contradictory; thus, further studies are needed. This study aimed to investigate whether in vitro exposure to 0.1 μM permethrin and malathion at 0, 24, 48 and 72 h after cell culture initiation induced changes in the gene expression and DNA methylation in mononuclear cells from bone marrow and peripheral blood (BMMCs, PBMCs). Both pesticides induced several gene expression modifications in both tissues. Through gene ontology analysis, we found that permethrin deregulates ion channels in PBMCs and BMMCs and that malathion alters genes coding proteins with nucleic acid binding capacity, which was also observed in PBMCs exposed to permethrin. Additionally, we found that both insecticides deregulate genes coding proteins with chemotaxis functions, ion channels, and cytokines. Several genes deregulated in this study are potentially associated with cancer onset and development, and some of them have been reported to be deregulated in hematological cancer. We found that permethrin does not induce DNA hypermethylation but can induce hypomethylation, and that malathion generated both types of events. Our results suggest that these pesticides have the potential to modify gene expression through changes in promoter DNA methylation and potentially through other mechanisms that should be investigated. MDPI 2023-03-26 /pmc/articles/PMC10094043/ /pubmed/37047231 http://dx.doi.org/10.3390/ijms24076259 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Navarrete-Meneses, María del Pilar Salas-Labadía, Consuelo Juárez-Velázquez, María del Rocío Moreno-Lorenzana, Dafné Gómez-Chávez, Fernando Olaya-Vargas, Alberto Pérez-Vera, Patricia Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro |
title | Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro |
title_full | Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro |
title_fullStr | Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro |
title_full_unstemmed | Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro |
title_short | Exposure to Insecticides Modifies Gene Expression and DNA Methylation in Hematopoietic Tissues In Vitro |
title_sort | exposure to insecticides modifies gene expression and dna methylation in hematopoietic tissues in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10094043/ https://www.ncbi.nlm.nih.gov/pubmed/37047231 http://dx.doi.org/10.3390/ijms24076259 |
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