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Differential Expression of Serum TUG1, LINC00657, MiR-9, and MiR-106a in Diabetic Patients With and Without Ischemic Stroke

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Specialty Biology
Date 2022 Mar 3
PMID 35237654
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Abstract

Ischemic stroke is one of the serious complications of diabetes. Non-coding RNAs are established as promising biomarkers for diabetes and its complications. The present research investigated the expression profiles of serum TUG1, LINC00657, miR-9, and miR-106a in diabetic patients with and without stroke. A total of 75 diabetic patients without stroke, 77 patients with stroke, and 71 healthy controls were recruited in the current study. The serum expression levels of TUG1, LINC00657, miR-9, and miR-106a were assessed using quantitative real-time polymerase chain reaction assays. We observed significant high expression levels of LINC00657 and miR-9 in the serum of diabetic patients without stroke compared to control participants. At the same time, we found marked increases of serum TUG1, LINC00657, and miR-9 and a marked decrease of serum miR-106a in diabetic patients who had stroke relative to those without stroke. Also, we revealed positive correlations between each of TUG1, LINC00657, and miR-9 and the National Institutes of Health Stroke Scale (NIHSS). However, there was a negative correlation between miR-106a and NIHSS. Finally, we demonstrated a negative correlation between LINC00657 and miR-106a in diabetic patients with stroke. Serum non-coding RNAs, TUG1, LINC00657, miR-9, and miR-106a displayed potential as novel molecular biomarkers for diabetes complicated with stroke, suggesting that they might be new therapeutic targets for the treatment of diabetic patients with stroke.

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References
1.
Hu D, Wang Y, Zhang H, Kong D . Identification of miR-9 as a negative factor of insulin secretion from beta cells. J Physiol Biochem. 2018; 74(2):291-299. DOI: 10.1007/s13105-018-0615-3. View

2.
Duan W, Du L, Jiang X, Wang R, Yan S, Xie Y . Identification of a serum circulating lncRNA panel for the diagnosis and recurrence prediction of bladder cancer. Oncotarget. 2016; 7(48):78850-78858. PMC: 5346682. DOI: 10.18632/oncotarget.12880. View

3.
Koutsis G, Siasos G, Spengos K . The emerging role of microRNA in stroke. Curr Top Med Chem. 2013; 13(13):1573-88. DOI: 10.2174/15680266113139990106. View

4.
Wang W, Wang Y, Ma P, Xu T, Shu Y . Taurine‑upregulated gene 1: A vital long non‑coding RNA associated with cancer in humans (Review). Mol Med Rep. 2017; 16(5):6467-6471. DOI: 10.3892/mmr.2017.7472. View

5.
Kitagawa M, Kitagawa K, Kotake Y, Niida H, Ohhata T . Cell cycle regulation by long non-coding RNAs. Cell Mol Life Sci. 2013; 70(24):4785-94. PMC: 3830198. DOI: 10.1007/s00018-013-1423-0. View