Dysregulations of MicroRNA and Gene Expression in Chronic Venous Disease

被引:17
作者
Zalewski, Daniel P. [1 ]
Ruszel, Karol P. [2 ]
Stepniewski, Andrzej [3 ]
Galkowski, Dariusz [4 ]
Bogucki, Jacek [2 ]
Komsta, Lukasz [5 ]
Kolodziej, Przemyslaw [1 ]
Chmiel, Paulina [1 ]
Zubilewicz, Tomasz [6 ]
Feldo, Marcin [6 ]
Kocki, Janusz [2 ]
Bogucka-Kocka, Anna [1 ]
机构
[1] Med Univ Lublin, Chair & Dept Biol & Genet, 4a Chodzki St, PL-20093 Lublin, Poland
[2] Med Univ Lublin, Dept Clin Genet, Chair Med Genet, 11 Radziwillowska St, PL-20080 Lublin, Poland
[3] Univ Marie Curie Sklodowska, Ecotech Complex Analyt & Programme Ctr Adv Enviro, 39 Gleboka St, PL-20612 Lublin, Poland
[4] Rutgers Robert Wood Johnson Med Sch, Dept Pathol & Lab Med, One Robert Wood Johnson Pl, New Brunswick, NJ 08903 USA
[5] Med Univ Lublin, Chair & Dept Med Chem, 4 Jaczewskiego St, PL-20090 Lublin, Poland
[6] Med Univ Lublin, Chair & Dept Vasc Surg & Angiol, 11 Staszica St, PL-20081 Lublin, Poland
关键词
chronic venous disease; CVD; varicose veins; miRNA; microRNA; gene; expression; next generation sequencing; biomarker; CLINICAL-PRACTICE-GUIDELINES; VARICOSE-VEINS; VASCULAR INFLAMMATION; PERIPHERAL-BLOOD; PROTEIN; CELLS; IDENTIFICATION; ANGIOGENESIS; INVOLVEMENT; PROGRESSION;
D O I
10.3390/jcm9051251
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic venous disease (CVD) is a vascular disease of lower limbs with high prevalence worldwide. Pathologic features include varicose veins, venous valves dysfunction and skin ulceration resulting from dysfunction of cell proliferation, apoptosis and angiogenesis. These processes are partly regulated by microRNA (miRNA)-dependent modulation of gene expression, pointing to miRNA as a potentially important target in diagnosis and therapy of CVD progression. The aim of the study was to analyze alterations of miRNA and gene expression in CVD, as well as to identify miRNA-mediated changes in gene expression and their potential link to CVD development. Using next generation sequencing, miRNA and gene expression profiles in peripheral blood mononuclear cells of subjects with CVD in relation to healthy controls were studied. Thirty-one miRNAs and 62 genes were recognized as potential biomarkers of CVD using DESeq2, Uninformative Variable Elimination by Partial Least Squares (UVE-PLS) and ROC (Receiver Operating Characteristics) methods. Regulatory interactions between potential biomarker miRNAs and genes were projected. Functional analysis of microRNA-regulated genes revealed terms closely related to cardiovascular diseases and risk factors. The study shed new light on miRNA-dependent regulatory mechanisms involved in the pathology of CVD. MicroRNAs and genes proposed as CVD biomarkers may be used to develop new diagnostic and therapeutic methods.
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页数:23
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