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Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model

DNA methylation is an epigenetic mechanism that is crucial for mammalian development and genomic stability. Aberrant DNA methylation changes have been detected not only in malignant tumor tissues; the decrease of global DNA methylation levels is also characteristic for aging. The consumption of extr...

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Autores principales: Szabo, Laszlo, Molnar, Richard, Tomesz, Andras, Deutsch, Arpad, Darago, Richard, Varjas, Timea, Ritter, Zsombor, Szentpeteri, Jozsef L., Andreidesz, Kitti, Mathe, Domokos, Hegedüs, Imre, Sik, Attila, Budan, Ferenc, Kiss, Istvan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878525/
https://www.ncbi.nlm.nih.gov/pubmed/35215560
http://dx.doi.org/10.3390/nu14040908
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author Szabo, Laszlo
Molnar, Richard
Tomesz, Andras
Deutsch, Arpad
Darago, Richard
Varjas, Timea
Ritter, Zsombor
Szentpeteri, Jozsef L.
Andreidesz, Kitti
Mathe, Domokos
Hegedüs, Imre
Sik, Attila
Budan, Ferenc
Kiss, Istvan
author_facet Szabo, Laszlo
Molnar, Richard
Tomesz, Andras
Deutsch, Arpad
Darago, Richard
Varjas, Timea
Ritter, Zsombor
Szentpeteri, Jozsef L.
Andreidesz, Kitti
Mathe, Domokos
Hegedüs, Imre
Sik, Attila
Budan, Ferenc
Kiss, Istvan
author_sort Szabo, Laszlo
collection PubMed
description DNA methylation is an epigenetic mechanism that is crucial for mammalian development and genomic stability. Aberrant DNA methylation changes have been detected not only in malignant tumor tissues; the decrease of global DNA methylation levels is also characteristic for aging. The consumption of extra virgin olive oil (EVOO) as part of a balanced diet shows preventive effects against age-related diseases and cancer. On the other hand, consuming trans fatty acids (TFA) increases the risk of cardiovascular diseases as well as cancer. The aim of the study was to investigate the LINE-1 retrotransposon (L1-RTP) DNA methylation pattern in liver, kidney, and spleen of mice as a marker of genetic instability. For that, mice were fed with EVOO or TFA and were pretreated with environmental carcinogen 7,12-dimethylbenz[a]anthracene (DMBA)—a harmful substance known to cause L1-RTP DNA hypomethylation. Our results show that DMBA and its combination with TFA caused significant L1-RTP DNA hypomethylation compared to the control group via inhibition of DNA methyltransferase (DNMT) enzymes. EVOO had the opposite effect by significantly decreasing DMBA and DMBA + TFA-induced hypomethylation, thereby counteracting their effects.
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spelling pubmed-88785252022-02-26 Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model Szabo, Laszlo Molnar, Richard Tomesz, Andras Deutsch, Arpad Darago, Richard Varjas, Timea Ritter, Zsombor Szentpeteri, Jozsef L. Andreidesz, Kitti Mathe, Domokos Hegedüs, Imre Sik, Attila Budan, Ferenc Kiss, Istvan Nutrients Article DNA methylation is an epigenetic mechanism that is crucial for mammalian development and genomic stability. Aberrant DNA methylation changes have been detected not only in malignant tumor tissues; the decrease of global DNA methylation levels is also characteristic for aging. The consumption of extra virgin olive oil (EVOO) as part of a balanced diet shows preventive effects against age-related diseases and cancer. On the other hand, consuming trans fatty acids (TFA) increases the risk of cardiovascular diseases as well as cancer. The aim of the study was to investigate the LINE-1 retrotransposon (L1-RTP) DNA methylation pattern in liver, kidney, and spleen of mice as a marker of genetic instability. For that, mice were fed with EVOO or TFA and were pretreated with environmental carcinogen 7,12-dimethylbenz[a]anthracene (DMBA)—a harmful substance known to cause L1-RTP DNA hypomethylation. Our results show that DMBA and its combination with TFA caused significant L1-RTP DNA hypomethylation compared to the control group via inhibition of DNA methyltransferase (DNMT) enzymes. EVOO had the opposite effect by significantly decreasing DMBA and DMBA + TFA-induced hypomethylation, thereby counteracting their effects. MDPI 2022-02-21 /pmc/articles/PMC8878525/ /pubmed/35215560 http://dx.doi.org/10.3390/nu14040908 Text en © 2022 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
Szabo, Laszlo
Molnar, Richard
Tomesz, Andras
Deutsch, Arpad
Darago, Richard
Varjas, Timea
Ritter, Zsombor
Szentpeteri, Jozsef L.
Andreidesz, Kitti
Mathe, Domokos
Hegedüs, Imre
Sik, Attila
Budan, Ferenc
Kiss, Istvan
Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model
title Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model
title_full Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model
title_fullStr Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model
title_full_unstemmed Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model
title_short Olive Oil Improves While Trans Fatty Acids Further Aggravate the Hypomethylation of LINE-1 Retrotransposon DNA in an Environmental Carcinogen Model
title_sort olive oil improves while trans fatty acids further aggravate the hypomethylation of line-1 retrotransposon dna in an environmental carcinogen model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8878525/
https://www.ncbi.nlm.nih.gov/pubmed/35215560
http://dx.doi.org/10.3390/nu14040908
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