4.6 Article

Circulating Extracellular-Vesicle-Incorporated MicroRNAs as Potential Biomarkers for Ischemic Stroke in Patients With Cancer

Journal

JOURNAL OF STROKE
Volume 25, Issue 2, Pages 251-+

Publisher

KOREAN STROKE SOC
DOI: 10.5853/jos.2022.02327

Keywords

Cancer; Stroke; Coagulopathy; Biomarker; Extracellular vesicle; MicroRNA

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This study aimed to evaluate the potential use of extracellular-vesicle-incorporated miRNAs as biomarkers for cancer-related stroke. The results showed that miR-205-5p, miR-645, and miR-646 were specifically incorporated into microvesicles in patients with cancer-related stroke, cancer controls, and stroke controls. The expression levels of these miRNAs could be used to differentiate patients with cancer-stroke from cancer-controls and stroke controls. Further studies are needed to confirm the diagnostic role of miRNAs in stroke patients and to investigate the roles of miRNAs in cancer patients.
Background and Purpose This study aimed to evaluate whether extracellular-vesicle-incorporated microRNAs (miRNAs) are potential biomarkers for cancer-related stroke.Methods This cohort study compared patients with active cancer who had embolic stroke of unknown sources (cancer-stroke group) with patients with only cancer, patients with only stroke, and healthy individuals (control groups). The expression profiles of miRNAs encapsulated in plasma exosomes and microvesicles were evaluated using microarray and validated using quantitative real-time polymerase chain reaction. The XENO-QTM miRNA assay technology was used to determine the absolute copy numbers of individual miRNAs in an external validation cohort.Results This study recruited 220 patients, of which 45 had cancer-stroke, 76 were healthy controls, 39 were cancer controls, and 60 were stroke controls. Three miRNAs (miR-205-5p, miR-645, and miR-646) were specifically incorporated into microvesicles in patients with cancer-related stroke, cancer controls, and stroke controls. The area under the receiver operating characteristic curves of these three miRNAs were 0.7692-0.8510 for the differentiation of patients with cancer-stroke from cancer-controls and 0.8077-0.8846 for the differentiation of patients with cancer-stroke from stroke controls. The levels of several miRNAs were elevated in the plasma exosomes of patients with cancer, but were lower than those in plasma microvesicles. An in vivo study showed that systemic injection of miR-205-5p promoted the development of arterial thrombosis and elevation of D-dimer levels.Conclusion Stroke due to cancer-related coagulopathy was associated with deregulated expression of miRNAs, particularly microvesicle-incorporated miR-205-5p, miR-645, and miR-646. Further prospective studies of extracellular-vesicle-incorporated miRNAs are required to confirm the diagnostic role of miRNAs in patients with stroke and to screen the roles of miRNAs in patients with cancer.

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