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Circulating exosomes and exosomal lncRNA HIF1A-AS1 in atherosclerosis
Yingge Wang1,2,3,4,5,6, Jingyan Liang1,2,3,4,5, Jiang Xu2,6
1Department of Anatomy, Medical College, Yangzhou University Yangzhou, China.
Insights
Exosomes and exosomal long non-coding RNA HIF1A-AS1 show promise as diagnostic biomarkers for atherosclerosis. Elevated levels of both were found in patients, indicating their potential for early disease detection.
Area of Science:
- Biochemistry
- Molecular Biology
- Cardiovascular Research
Background:
- Exosomes mediate intercellular communication and transfer long non-coding RNAs (lncRNAs).
- lncRNA HIF1A-AS1, transferable via exosomes, is implicated in atherosclerosis pathogenesis.
- This study investigates the diagnostic utility of exosomes and exosomal lncRNA HIF1A-AS1 in atherosclerosis.
Purpose of the Study:
- To evaluate the diagnostic accuracy of exosome concentration and exosomal lncRNA HIF1A-AS1 expression in atherosclerosis patients.
- To determine the correlation between exosome concentration and lncRNA HIF1A-AS1 levels in atherosclerosis.
Main Methods:
- Plasma samples from 35 atherosclerosis patients and 28 healthy controls were analyzed.
- Exosomes were isolated and quantified using flow cytometry.
- Exosomal RNA was extracted, and lncRNA HIF1A-AS1 expression was measured via qRT-PCR.
Main Results:
- Exosome concentration and exosomal lncRNA HIF1A-AS1 expression were significantly higher in atherosclerosis patients compared to healthy controls.
- A positive correlation was observed between exosome concentration and lncRNA HIF1A-AS1 expression.
- Receiver operating characteristic (ROC) curve analysis yielded area values of 0.856 for exosomes and 0.823 for lncRNA HIF1A-AS1.
Conclusions:
- Exosomes and exosomal lncRNA HIF1A-AS1 demonstrate potential as novel biomarkers for atherosclerosis diagnosis.
- These findings suggest a role for exosomal components in atherosclerosis detection and potentially in disease mechanisms.
Background:
Exosomes which mainly function in intercellular communication and lncRNA HIF1A-AS1 which can be transferred by exosomes, have been shown to play a significant role in atherosclerosis. This study aims to explore the diagnostic value of exosomes and exosomal lncRNA HIF in atherosclerosis.
Methods:
Plasma sample from 35 patients with atherosclerosis and from 28 healthy adults were collected for further investigation. The exosomes were extracted from the plasma sample and then the concentration of exosomes was measured by flow cytometry. Then the exosomal RNA was isolated and exosomal lncRNA HIF1A-AS1 was quantified using real-time polymerase chain reaction (qRT-PCR). Finally, the concentration of exosomes and the expression level of exosomal lncRNA HIF1A-AS1 were analyzed using Spearman's correlation test, and receiver operating characteristic (ROC) curves were used for evaluation of diagnostic accuracy of exosomes and exosomal lncRNA HIF1A-AS1.
Results:
The concentration of exosomes was significantly higher in patients with atherosclerosis than that in healthy people, the same as the expression level of exosomal lncRNA HIF1A-AS1. Furthermore, the result of Spearman's correlation test indicated that there was a positive correlation between them. Last, we also showed that the area values under the ROC curves of exosomes and lncRNA HIF1A-AS1 were 0.856 and 0.823, respectively.
Conclusion:
Exosomes and exosomal lncRNA HIF1A-AS1 could act as potential biomarkers for atherosclerosis.
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