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Application of OpenArray RT-qPCR for identification of microRNA expression signatures of lower extremity artery disease.
Zalewski, Daniel P; Ruszel, Karol P; Stepniewski, Andrzej; Galkowski, Dariusz; Feldo, Marcin; Kocki, Janusz; Bogucka-Kocka, Anna.
  • Zalewski DP; Chair and Department of Biology and Genetics, Medical University of Lublin, 4a Chodzki St., 20-093, Lublin, Poland. daniel.zalewski@umlub.pl.
  • Ruszel KP; Department of Clinical Genetics, Chair of Medical Genetics, Medical University of Lublin, 11 Radziwillowska St., 20-080, Lublin, Poland.
  • Stepniewski A; Ecotech Complex Analytical and Programme Centre for Advanced Environmentally Friendly Technologies, University of Marie Curie-Sklodowska, 39 Gleboka St., 20-612, Lublin, Poland.
  • Galkowski D; Department of Pathology and Laboratory Medicine, Rutgers-Robert Wood Johnson Medical School, One Robert Wood Johnson Place, New Brunswick, NJ, 08903-0019, USA.
  • Feldo M; Chair and Department of Vascular Surgery and Angiology, Medical University of Lublin, 11 Staszica St., 20-081, Lublin, Poland.
  • Kocki J; Department of Clinical Genetics, Chair of Medical Genetics, Medical University of Lublin, 11 Radziwillowska St., 20-080, Lublin, Poland.
  • Bogucka-Kocka A; Chair and Department of Biology and Genetics, Medical University of Lublin, 4a Chodzki St., 20-093, Lublin, Poland.
J Appl Genet ; 63(3): 497-512, 2022 Sep.
Article en En | MEDLINE | ID: mdl-35366714
ABSTRACT
Lower extremity artery disease (LEAD) is an underestimated chronic vascular disease caused by the formation of atherosclerotic plaques in the lower limb arteries. The pathological processes underlying this disease are regulated by many various factors, including microRNAs (miRNAs). miRNAs constitute a pool of small, non-coding RNAs with a gene expression modulatory function. In the presented study, differentially expressed miRNAs were identified in peripheral blood mononuclear cells from 18 patients with LEAD compared to 10 healthy volunteers using OpenArray RT-qPCR. Sixteen miRNAs were significantly differentially expressed in the LEAD group. Four out of them, hsa-miR-138-5p, -34a-3p, -34a-5p, and -766-3p, were consistent with a previous next-generation sequencing study. The in silico analysis performed for these four miRNAs showed associations with vascular smooth muscle cells differentiation, inflammation, and apoptosis, potentially resulting from modulation of genes involved in cell cycle, cellular adhesion, and Notch signaling. The presented study expands our knowledge on the role of miRNA in the pathology of LEAD, providing potential candidates for biomarkers of this disease.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Perfilación de la Expresión Génica / MicroARNs Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Perfilación de la Expresión Génica / MicroARNs Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article