Modulation of DNA methylation by one-carbon metabolism: a milestone for healthy aging.
Sang-Woon ChoiSimonetta FrisoPublished in: Nutrition research and practice (2023)
Healthy aging can be defined as an extended lifespan and health span. Nutrition has been regarded as an important factor in healthy aging, because nutrients, bioactive food components, and diets have demonstrated beneficial effects on aging hallmarks such as oxidative stress, mitochondrial function, apoptosis and autophagy, genomic stability, and immune function. Nutrition also plays a role in epigenetic regulation of gene expression, and DNA methylation is the most extensively investigated epigenetic phenomenon in aging. Interestingly, age-associated DNA methylation can be modulated by one-carbon metabolism or inhibition of DNA methyltransferases. One-carbon metabolism ultimately controls the balance between the universal methyl donor S-adenosylmethionine and the methyltransferase inhibitor S-adenosylhomocysteine. Water-soluble B-vitamins such as folate, vitamin B6, and vitamin B12 serve as coenzymes for multiple steps in one-carbon metabolism, whereas methionine, choline, betaine, and serine act as methyl donors. Thus, these one-carbon nutrients can modify age-associated DNA methylation and subsequently alter the age-associated physiologic and pathologic processes. We cannot elude aging per se but we may at least change age-associated DNA methylation, which could mitigate age-associated diseases and disorders.
Keyphrases
- dna methylation
- gene expression
- genome wide
- oxidative stress
- copy number
- physical activity
- endoplasmic reticulum stress
- water soluble
- cell death
- healthcare
- public health
- heavy metals
- squamous cell carcinoma
- multidrug resistant
- mental health
- cell proliferation
- radiation therapy
- weight loss
- neoadjuvant chemotherapy
- health information
- climate change
- mass spectrometry
- locally advanced
- risk assessment
- cell free
- ischemia reperfusion injury
- circulating tumor cells
- circulating tumor
- tissue engineering