The Long Non-coding Road to Atherosclerosis.
Tatjana JosefsReinier Abraham BoonPublished in: Current atherosclerosis reports (2020)
LncRNAs can bind to proteins, DNA, and RNA regulating disease initiation and plaque growth as well as plaque stability in different cell types such as endothelial cells (ECs), vascular smooth muscle cells (VSMCs), and macrophages. A number of lncRNAs have been implicated in cholesterol homeostasis and foam cell formation such as LASER, LeXis, and CHROME. Among others, MANTIS, lncRNA-CCL2, and MALAT1 were shown to be involved in vascular inflammation. Further regulations include, but are not limited to, DNA damage response in ECs, phenotypic switch of VSMCs, and various cell death mechanisms. Interestingly, some lncRNAs are closely correlated with response to statin treatment, such as NEXN-AS1 or LASER. Additionally, some lncRNAs may serve as CVD biomarkers. LncRNAs are a potential novel therapeutic target to treat CVD, but research of lncRNA in atherosclerosis is still in its infancy. With increasing knowledge of the complex and diverse regulations of lncRNAs in the heterogeneous environment of atherosclerotic plaques, lncRNAs hold promise for their clinical translation in the near future.
Keyphrases
- vascular smooth muscle cells
- network analysis
- genome wide analysis
- genome wide identification
- cell death
- dna damage response
- cardiovascular disease
- endothelial cells
- coronary artery disease
- single cell
- angiotensin ii
- oxidative stress
- type diabetes
- machine learning
- cell proliferation
- physical activity
- dna damage
- weight gain
- current status
- low density lipoprotein
- cell free
- body mass index
- mass spectrometry
- signaling pathway
- circulating tumor cells
- deep learning