Oxysterols in the pathogenesis of major chronic diseases.Redox Biol. 2013 Jan 31; 1:125-30.RB
Abstract
Pathological accumulation of 27-carbon intermediates or end-products of cholesterol metabolism, named oxysterols, may contribute to the onset and especially to the development of major chronic diseases in which inflammation, but also oxidative damage and to a certain extent cell death, are hallmarks and primary mechanisms of progression. Indeed, certain oxysterols exercise strong pro-oxidant and pro-inflammatory effects at concentrations detectable in the lesions typical of atherosclerosis, neurodegenerative diseases, inflammatory bowel diseases, age-related macular degeneration, and other pathological conditions characterized by altered cholesterol uptake and/or metabolism.
Links
Pub Type(s)
Journal Article
Review
Language
eng
PubMed ID
24024145
Citation
Poli, Giuseppe, et al. "Oxysterols in the Pathogenesis of Major Chronic Diseases." Redox Biology, vol. 1, 2013, pp. 125-30.
Poli G, Biasi F, Leonarduzzi G. Oxysterols in the pathogenesis of major chronic diseases. Redox Biol. 2013;1:125-30.
Poli, G., Biasi, F., & Leonarduzzi, G. (2013). Oxysterols in the pathogenesis of major chronic diseases. Redox Biology, 1, 125-30. https://doi.org/10.1016/j.redox.2012.12.001
Poli G, Biasi F, Leonarduzzi G. Oxysterols in the Pathogenesis of Major Chronic Diseases. Redox Biol. 2013 Jan 31;1:125-30. PubMed PMID: 24024145.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Oxysterols in the pathogenesis of major chronic diseases.
AU - Poli,Giuseppe,
AU - Biasi,Fiorella,
AU - Leonarduzzi,Gabriella,
Y1 - 2013/01/31/
PY - 2012/11/23/received
PY - 2012/12/03/accepted
PY - 2013/9/12/entrez
PY - 2013/9/12/pubmed
PY - 2013/9/12/medline
KW - 24-OH, 24-hydroxycholesterol
KW - 27-OH, 27-hydroxycholesterol
KW - 7-K, 7-ketocholesterol
KW - 7α-OH, 7α-hydroxycholesterol
KW - 7β-OH, 7β-hydroxycholesterol
KW - AMD, Age-related macular degeneration
KW - AP-1, Activator protein-1
KW - Aβ, Amyloid-β
KW - ERK1/2, Extracellular signaling-regulated kinase 1/2
KW - FXR, Farnesoid X receptor
KW - Human chronic diseases
KW - IBD, Inflammatory bowel diseases
KW - ICAM, Intercellular adhesion molecule-1
KW - IL, Interleukin
KW - Inflammation
KW - JNK, c-Jun N-terminal
KW - LDL, Low density lipoprotein
KW - LXR, Liver X receptor
KW - MAPK, Mitogen-activated protein kinase
KW - MCP-1, Monocyte chemotactic protein-1
KW - MIP-1β, Monocyte inflammatory protein-1β
KW - MMP, Matrix metalloproteinase
KW - NF-κB, Nuclear factor-κB
KW - Oxidative stress
KW - Oxysterols
KW - PKC, Protein kinase C
KW - ROS, Reactive oxygen species
KW - TGFβ1, Transforming growth factor β1
KW - TIMP, Tissue inhibitors of metalloproteinases
KW - TNF-α, Tumor necrosis factor-α
KW - VCAM-1, Vascular cell adhesion molecule-1
KW - α-EPOX, 5α,6α-epoxycholesterol
KW - β-EPOX, 5β,6β-epoxycholesterol
SP - 125
EP - 30
JF - Redox biology
JO - Redox Biol
VL - 1
N2 - Pathological accumulation of 27-carbon intermediates or end-products of cholesterol metabolism, named oxysterols, may contribute to the onset and especially to the development of major chronic diseases in which inflammation, but also oxidative damage and to a certain extent cell death, are hallmarks and primary mechanisms of progression. Indeed, certain oxysterols exercise strong pro-oxidant and pro-inflammatory effects at concentrations detectable in the lesions typical of atherosclerosis, neurodegenerative diseases, inflammatory bowel diseases, age-related macular degeneration, and other pathological conditions characterized by altered cholesterol uptake and/or metabolism.
SN - 2213-2317
UR - https://www.unboundmedicine.com/medline/citation/24024145/full_citation
L2 - https://linkinghub.elsevier.com/retrieve/pii/REDOX6
DB - PRIME
DP - Unbound Medicine
ER -

