Ten long non-coding RNAs, notably MALAT1, have been implicated in venous thromboembolism pathogenesis, while five others affect the expression of the anticoagulant protein TFPI2.
What is the role of long non-coding RNAs in the pathogenesis of venous thromboembolism?
Current evidence implicates ten lncRNAs, notably MALAT1, in VTE pathogenesis, suggesting potential future roles as biomarkers or therapeutic targets.
Venous thromboembolism (VTE), a common condition in Western countries, is a cardiovascular disorder that arises due to haemostatic irregularities, which lead to thrombus generation inside veins. Even with successful treatment, the resulting disease spectrum of complications considerably affects the patient's quality of life, potentially leading to death. Cumulative data indicate that long non-coding RNAs (lncRNAs) may have a role in VTE pathogenesis. However, the clinical usefulness of these RNAs as biomarkers and potential therapeutic targets for VTE management is yet unclear. Thus, this article reviewed the emerging evidence on lncRNAs associated with VTE and with the activity of the coagulation system, which has a central role in disease pathogenesis. Until now, ten lncRNAs have been implicated in VTE pathogenesis, among which MALAT1 is the one with more evidence. Meanwhile, five lncRNAs have been reported to affect the expression of TFPI2, an important anticoagulant protein, but none with a described role in VTE development. More investigation in this field is needed as lncRNAs may help dissect VTE pathways, aiding in disease prediction, prevention and treatment.
Marques et al. (Fri,) conducted a review in Venous thromboembolism. Long non-coding RNAs (lncRNAs) was evaluated on Role of lncRNAs in VTE pathogenesis. Ten long non-coding RNAs, notably MALAT1, have been implicated in venous thromboembolism pathogenesis, while five others affect the expression of the anticoagulant protein TFPI2.
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