The role of AMPK in metabolism and its influence on DNA damage repair.
Michał SzewczukKarolina BoguszewskaJulia Kaźmierczak-BarańskaBoleslaw T KarwowskiPublished in: Molecular biology reports (2020)
One of the most complex health disproportions in the human body is the metabolic syndrome (MetS). It can result in serious health consequences such as type 2 diabetes mellitus, atherosclerosis or insulin resistance. The center of energy regulation in human is AMP-activated protein kinase (AMPK), which modulates cells' metabolic pathways and protects them against negative effects of metabolic stress, e.g. reactive oxygen species. Moreover, recent studies show the relationship between the AMPK activity and the regulation of DNA damage repair such as base excision repair (BER) system, which is presented in relation to the influence of MetS on human genome. Hence, AMPK is studied not only in the field of counteracting MetS but also prevention of genetic alterations and cancer development. Through understanding AMPK pathways and its role in cells with damaged DNA it might be possible to improve cell's repair processes and develop new therapies. This review presents AMPK role in eukaryotic cells and focuses on the relationship between AMPK activity and the regulation of BER system through its main component-8-oxoguanine glycosylase (OGG1).
Keyphrases
- protein kinase
- dna damage
- skeletal muscle
- induced apoptosis
- endothelial cells
- insulin resistance
- metabolic syndrome
- cell cycle arrest
- dna repair
- public health
- oxidative stress
- healthcare
- reactive oxygen species
- endoplasmic reticulum stress
- induced pluripotent stem cells
- pluripotent stem cells
- mental health
- cell proliferation
- adipose tissue
- gene expression
- cell death
- dna methylation
- health information
- cell therapy
- circulating tumor
- mesenchymal stem cells
- high fat diet
- social media
- cardiovascular risk factors
- glycemic control
- polycystic ovary syndrome
- case control
- weight loss
- heat stress
- stress induced
- circulating tumor cells
- lymph node metastasis