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CXCL16 in Vascular Pathology Research: from Macro Effects to microRNAs

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2015
814.pdf (1.009Mb)
Authors
Jovanović, Ivan G.
Živković, Maja
Đurić, Tamara
Popović, Milan
Alavantić, Dragan
Stanković, Aleksandra
Review (Published version)
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Abstract
Chemokines and their receptors have become significant factors in atherosclerosis research. CXCL16 is a multifunctional agent located on a separate locus to all other known chemokines and binds only to its unique receptor named CXCR6. As a scavenger receptor, adhesion molecule, and chemokine, it quickly became an interesting target in atherosclerosis research as all its functions have a role in vascular pathology. The investigation of the role of CXCL16 in atherosclerosis, although shown in in vitro studies, animal knockout models, and CXCL16 gene polymorphisms, haplotypes, and circulating levels, still shows puzzling results. Genetic and epigenetic studies have just scratched the surface of research necessary for a better assessment of the significance and perspective of this marker in plaque development and progression. In this review, we will summarize current knowledge about CXCL16 in atherosclerosis. Additionally, we will point out the importance of bioinformatics tools for the de...tection of potentially new CXCL16 regulatory networks through microRNA activity. This review aims to provide a better understanding of the underlying mechanisms, define more specific biomarkers, and discover new therapeutic targets.

Keywords:
CXCL16 chemokine / gene / Expression / microRNA / Atherosclerosis
Source:
Journal of Atherosclerosis and Thrombosis, 2015, 22, 10, 1012-1024
Funding / projects:
  • An integral study to identify the regional genetic and environmental risk factors for the common noncommunicable diseases in the human population of Serbia - INGEMA_S (RS-41028)
  • Genetic basis of human vascular and inflammatory diseases (RS-175085)

DOI: 10.5551/jat.29942

ISSN: 1340-3478; 1880-3873

PubMed: 26289084

WoS: 000365182000002

Scopus: 2-s2.0-84943264040
[ Google Scholar ]
12
13
URI
https://vinar.vin.bg.ac.rs/handle/123456789/818
Collections
  • WoS Import
Institution/Community
Vinča
TY  - JOUR
AU  - Jovanović, Ivan G.
AU  - Živković, Maja
AU  - Đurić, Tamara
AU  - Popović, Milan
AU  - Alavantić, Dragan
AU  - Stanković, Aleksandra
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/818
AB  - Chemokines and their receptors have become significant factors in atherosclerosis research. CXCL16 is a multifunctional agent located on a separate locus to all other known chemokines and binds only to its unique receptor named CXCR6. As a scavenger receptor, adhesion molecule, and chemokine, it quickly became an interesting target in atherosclerosis research as all its functions have a role in vascular pathology. The investigation of the role of CXCL16 in atherosclerosis, although shown in in vitro studies, animal knockout models, and CXCL16 gene polymorphisms, haplotypes, and circulating levels, still shows puzzling results. Genetic and epigenetic studies have just scratched the surface of research necessary for a better assessment of the significance and perspective of this marker in plaque development and progression. In this review, we will summarize current knowledge about CXCL16 in atherosclerosis. Additionally, we will point out the importance of bioinformatics tools for the detection of potentially new CXCL16 regulatory networks through microRNA activity. This review aims to provide a better understanding of the underlying mechanisms, define more specific biomarkers, and discover new therapeutic targets.
T2  - Journal of Atherosclerosis and Thrombosis
T1  - CXCL16 in Vascular Pathology Research: from Macro Effects to microRNAs
VL  - 22
IS  - 10
SP  - 1012
EP  - 1024
DO  - 10.5551/jat.29942
ER  - 
@article{
author = "Jovanović, Ivan G. and Živković, Maja and Đurić, Tamara and Popović, Milan and Alavantić, Dragan and Stanković, Aleksandra",
year = "2015",
abstract = "Chemokines and their receptors have become significant factors in atherosclerosis research. CXCL16 is a multifunctional agent located on a separate locus to all other known chemokines and binds only to its unique receptor named CXCR6. As a scavenger receptor, adhesion molecule, and chemokine, it quickly became an interesting target in atherosclerosis research as all its functions have a role in vascular pathology. The investigation of the role of CXCL16 in atherosclerosis, although shown in in vitro studies, animal knockout models, and CXCL16 gene polymorphisms, haplotypes, and circulating levels, still shows puzzling results. Genetic and epigenetic studies have just scratched the surface of research necessary for a better assessment of the significance and perspective of this marker in plaque development and progression. In this review, we will summarize current knowledge about CXCL16 in atherosclerosis. Additionally, we will point out the importance of bioinformatics tools for the detection of potentially new CXCL16 regulatory networks through microRNA activity. This review aims to provide a better understanding of the underlying mechanisms, define more specific biomarkers, and discover new therapeutic targets.",
journal = "Journal of Atherosclerosis and Thrombosis",
title = "CXCL16 in Vascular Pathology Research: from Macro Effects to microRNAs",
volume = "22",
number = "10",
pages = "1012-1024",
doi = "10.5551/jat.29942"
}
Jovanović, I. G., Živković, M., Đurić, T., Popović, M., Alavantić, D.,& Stanković, A.. (2015). CXCL16 in Vascular Pathology Research: from Macro Effects to microRNAs. in Journal of Atherosclerosis and Thrombosis, 22(10), 1012-1024.
https://doi.org/10.5551/jat.29942
Jovanović IG, Živković M, Đurić T, Popović M, Alavantić D, Stanković A. CXCL16 in Vascular Pathology Research: from Macro Effects to microRNAs. in Journal of Atherosclerosis and Thrombosis. 2015;22(10):1012-1024.
doi:10.5551/jat.29942 .
Jovanović, Ivan G., Živković, Maja, Đurić, Tamara, Popović, Milan, Alavantić, Dragan, Stanković, Aleksandra, "CXCL16 in Vascular Pathology Research: from Macro Effects to microRNAs" in Journal of Atherosclerosis and Thrombosis, 22, no. 10 (2015):1012-1024,
https://doi.org/10.5551/jat.29942 . .

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