MicroRNA expression signature in human abdominal aortic aneurysms

Autor: Irene Hinterseher, James R. Elmore, John L. Gray, Matthew C Pahl, Charles M. Schworer, David P. Franklin, David J. Carey, Helena Kuivaniemi, Thomas C. Peeler, Gerard Tromp, Gabor Gäbel, Kimberly Derr
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Male
lcsh:Internal medicine
Microarray
lcsh:QH426-470
Apoptosis
macromolecular substances
030204 cardiovascular system & hematology
Biology
Bioinformatics
Real-Time Polymerase Chain Reaction
Vascular biology
03 medical and health sciences
0302 clinical medicine
Gene expression
microRNA
Genetics
Humans
Genetics(clinical)
Gene Regulatory Networks
RNA
Messenger

lcsh:RC31-1245
Genetics (clinical)
030304 developmental biology
Aged
Oligonucleotide Array Sequence Analysis
Regulation of gene expression
0303 health sciences
Microarray analysis techniques
Gene Expression Profiling
miRNA-mRNA analysis
Reproducibility of Results
Microarray analysis
Middle Aged
Gene expression profiling
MicroRNAs
lcsh:Genetics
Real-time polymerase chain reaction
Gene Expression Regulation
cardiovascular system
Female
Network analysis
DNA microarray
Research Article
Aortic Aneurysm
Abdominal
Zdroj: BMC Medical Genomics, Vol 5, Iss 1, p 25 (2012)
BMC Medical Genomics
ISSN: 1755-8794
Popis: Background Abdominal aortic aneurysm (AAA) is a dilatation of the aorta affecting most frequently elderly men. Histologically AAAs are characterized by inflammation, vascular smooth muscle cell apoptosis, and extracellular matrix degradation. The mechanisms of AAA formation, progression, and rupture are currently poorly understood. A previous mRNA expression study revealed a large number of differentially expressed genes between AAA and non-aneurysmal control aortas. MicroRNAs (miRNAs), small non-coding RNAs that are post-transcriptional regulators of gene expression, could provide a mechanism for the differential expression of genes in AAA. Methods To determine differences in miRNA levels between AAA (n = 5) and control (n = 5) infrarenal aortic tissues, a microarray study was carried out. Results were adjusted using Benjamini-Hochberg correction (adjusted p Results A microarray study identified eight miRNAs with significantly different expression levels between AAA and controls (adjusted p Conclusions Our genome-wide approach revealed several differentially expressed miRNAs in human AAA tissue suggesting that miRNAs play a role in AAA pathogenesis.
Databáze: OpenAIRE