Positive association between abdominal aortic diameter and serum collagen XVIII levels

Rašiová, Mária; Farkašová, Ľudmila; Koščo, Martin; Moščovič, Matej; Špak, Ľubomír; Petrášová, Darina; Tkáč, Ivan

doi:10.23736/s0392-9590.19.04222-6

Cited by 2 publications

(1 citation statement)

References 39 publications

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“…Simvastatin may inhibit NF-κB activity by inhibiting free radicals and TNF-α production, improving human AAA wall tissue ( Piechota-Polanczyk et al, 2012 ). Elevated Prdx-1 levels in the serum and tissues of AAA patients were associated with AAA size and the AAA growth rate ( Martinez-Pinna et al, 2011 ; Ramella et al, 2018 ; Rasiova et al, 2019 ). Prdx2 plays a role as a negative regulator of the pathological process of AAA ( Jeong et al, 2020 ; Martinez-Pinna et al, 2014 ).…”

Section: Discussionmentioning

confidence: 99%

Ageing- and AAA-associated differentially expressed proteins identified by proteomic analysis in mice

Ren

Tang

et al. 2022

PeerJ

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Background Abdominal aortic aneurysm (AAA) is a disease of high prevalence in old age, and its incidence gradually increases with increasing age. There were few studies about differences in the circulatory system in the incidence of AAA, mainly because younger patients with AAA are fewer and more comorbid nonatherosclerotic factors. Method We induced AAA in ApoE−/− male mice of different ages (10 or 24 weeks) and obtained plasma samples. After the top 14 most abundant proteins were detected, the plasma was analyzed by a proteomic study using the data-dependent acquisition (DDA) technique. The proteomic results were compared between different groups to identify age-related differentially expressed proteins (DEPs) in the circulation that contribute to AAA formation. Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and protein–protein interaction (PPI) network analyses were performed by R software. The top 10 proteins were determined with the MCC method of Cytoscape, and transcription factor (TF) prediction of the DEPs was performed with iRegulon (Cytoscape). Results The aortic diameter fold increase was higher in the aged group than in the youth group (p < 0.01). Overall, 92 DEPs related to age and involved in AAA formation were identified. GO analysis of the DEPs showed enrichment of the terms wounding healing, response to oxidative stress, regulation of body fluid levels, ribose phosphate metabolic process, and blood coagulation. The KEGG pathway analysis showed enrichment of the terms platelet activation, complement and coagulation cascades, glycolysis/gluconeogenesis, carbon metabolism, biosynthesis of amino acids, and ECM-receptor interaction. The top 10 proteins were Tpi1, Eno1, Prdx1, Ppia, Prdx6, Vwf, Prdx2, Fga, Fgg, and Fgb, and the predicted TFs of these proteins were Nfe2, Srf, Epas1, Tbp, and Hoxc8. Conclusion The identified proteins related to age and involved in AAA formation were associated with the response to oxidative stress, coagulation and platelet activation, and complement and inflammation pathways, and the TFs of these proteins might be potential targets for AAA treatments. Further experimental and biological studies are needed to elucidate the role of these age-associated and AAA-related proteins in the progression of AAA.

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