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Research Paper

MicroRNA-488 serves as a diagnostic marker for atherosclerosis and regulates the biological behavior of vascular smooth muscle cells

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Pages 4092-4099 | Received 28 Apr 2021, Accepted 02 Jul 2021, Published online: 21 Jul 2021

Figures & data

Table 1. Clinical data of the study population

Figure 1. The expression level of serum miR-488 in AS patients and the correlation study between miR-488 expression and CIMT. (a) The expression level of serum miR-488 was upregulated in AS patients compared with healthy controls. ***P < 0.001. (b) Serum miR-488 level was positively correlated with CIMT in patients in AS patients (r = 0.706, ***P < 0.001)

Figure 1. The expression level of serum miR-488 in AS patients and the correlation study between miR-488 expression and CIMT. (a) The expression level of serum miR-488 was upregulated in AS patients compared with healthy controls. ***P < 0.001. (b) Serum miR-488 level was positively correlated with CIMT in patients in AS patients (r = 0.706, ***P < 0.001)

Figure 2. A ROC curve was established to assess the specificity and sensitivity of miR-488 to differentiate between AS and healthy controls, the miR-488 has quite well performance with an AUC score of 0.892

Figure 2. A ROC curve was established to assess the specificity and sensitivity of miR-488 to differentiate between AS and healthy controls, the miR-488 has quite well performance with an AUC score of 0.892

Figure 3. Effects of miR-488 expression levels on cell proliferation and migration abilities in VSMCs cells. (a) qRT-PCR was used to analyze the expression level of miR-488 after transient transfection with miR-488 mimic/inhibitor (or mimic/inhibitor NC). (b) The CCK-8 assay was performed to study cell proliferation. (c) Cell migration abilities were assessed with Transwell assay. ***P < 0.001, *P < 0.05

Figure 3. Effects of miR-488 expression levels on cell proliferation and migration abilities in VSMCs cells. (a) qRT-PCR was used to analyze the expression level of miR-488 after transient transfection with miR-488 mimic/inhibitor (or mimic/inhibitor NC). (b) The CCK-8 assay was performed to study cell proliferation. (c) Cell migration abilities were assessed with Transwell assay. ***P < 0.001, *P < 0.05

Data availability statement

Corresponding authors may provide data and materials.