Sadeghi Tayebeh, Zaki-Dizaji Majid, Dolatabad Meisam Rostaminasab, Taheri Zahra
Department of Physiology, Ke.C., Islamic Azad University, Kerman, Iran.
Human Genetics Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
J Diabetes Metab Disord. 2025 Apr 22;24(1):106. doi: 10.1007/s40200-025-01619-3. eCollection 2025 Jun.
Pro-inflammatory molecules are key risk factors for coronary artery diseases (CAD). Therefore, the regulation of inflammatory responses plays a crucial role in CAD. Suppressor of cytokine signaling 4 (SOCS4) is a negative regulator of cytokine signaling may significantly contribute to the pathogenesis of CAD. Bioinformatics studies indicate that hsa-miR-568-5p can target SOCS4. This study aimed to evaluate the expression of hsa-miR-568-5p in patients with CAD and investigate its correlation with SOCS4 levels.
The study included 20 Iranian participants without artery stenosis and 40 with artery stenosis. The relative expression levels of hsa-miR-568-5p and SOCS4 were assessed using Real-Time PCR.
The findings revealed no significant difference in the expression levels of hsa-miR-568-5p and SOCS4 between the two groups. Also, correlations were not observed between hsa-miR-568-5p, SOCS4, and age in both the control and CAD patient groups.
While hsa-miR-568-5p regulates SOCS4 expression, and SOCS4 upregulation is implicated in coronary artery disease (CAD) protection, this study found no conclusive evidence supporting this relationship. Further research is warranted.
促炎分子是冠状动脉疾病(CAD)的关键危险因素。因此,炎症反应的调节在CAD中起着至关重要的作用。细胞因子信号转导抑制因子4(SOCS4)是细胞因子信号转导的负调节因子,可能在CAD的发病机制中起重要作用。生物信息学研究表明,hsa-miR-568-5p可以靶向SOCS4。本研究旨在评估CAD患者中hsa-miR-568-5p的表达,并探讨其与SOCS4水平的相关性。
该研究纳入了20名无动脉狭窄的伊朗参与者和40名有动脉狭窄的参与者。使用实时PCR评估hsa-miR-568-5p和SOCS4的相对表达水平。
研究结果显示,两组之间hsa-miR-568-5p和SOCS4的表达水平无显著差异。此外,在对照组和CAD患者组中,均未观察到hsa-miR-568-5p、SOCS4与年龄之间的相关性。
虽然hsa-miR-568-5p调节SOCS4的表达,且SOCS4上调与冠状动脉疾病(CAD)的保护有关,但本研究未发现支持这种关系的确凿证据。有必要进行进一步的研究。