4.7 Article

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

Journal

NUTRIENTS
Volume 14, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/nu14040908

Keywords

extra virgin olive oil; trans fatty acid; DMBA; LINE-1 methylation pattern

Funding

  1. European Union [712821, 739593]
  2. Ministry of Innovation and Technology of Hungary Thematic Excellence Program (TKP-BIOImaging at Semmelweis University)

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DNA methylation plays a crucial role in mammalian development and genomic stability. Aberrant changes in DNA methylation are associated with malignant tumor tissues and aging. Consuming extra virgin olive oil shows preventive effects against age-related diseases and cancer, while consuming trans fatty acids increases the risk of cardiovascular diseases and cancer. This study investigated the DNA methylation pattern of the LINE-1 retrotransposon in mouse liver, kidney, and spleen, and found that environmental carcinogen DMBA and its combination with trans fatty acids caused significant hypomethylation, which was counteracted by the consumption of extra virgin olive oil.
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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