Unveiling the therapeutic potential of miR-146a: Targeting innate inflammation in atherosclerosis

Azizah Puspitasari Ardinal, Alice Valeria Wiyono, Reza Ishak Estiko
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Abstract

Atherosclerosis is the foremost vascular disease, precipitating debilitating complications. Although therapeutic strategies have historically focused on reducing cholesterol deposition, recent insights emphasize the pivotal role of inflammation. Innate inflammation significantly contributes to plaque instability and rupture, underscoring the need for intervention across all disease stages. Numerous studies have highlighted the therapeutic potential of targeting innate immune pathways in atherosclerosis, revealing significant advancements in understanding the molecular mechanisms underlying inflammatory processes within arterial lesions. Notably, research has demonstrated that the modulation of microRNA-146a (miR-146a) expression impacts innate inflammation, effectively halts atherosclerosis progression, and enhances plaque stability by targeting interleukin-1 receptor-associated kinase (IRAK) and activating TNF receptor-associated factor 6 (TRAF6), a signalling pathway involving toll-like receptors (TLRs). Understanding the intricate mechanisms involved is crucial. This study provides a comprehensive analysis of the evidence and underlying mechanisms through which miR-146a exerts its effects. Integrating these findings into clinical practice may herald a transformative era in managing atherosclerotic cardiovascular disease.

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揭示 miR-146a 的治疗潜力:针对动脉粥样硬化中的先天性炎症。
动脉粥样硬化是最主要的血管疾病,会引发使人衰弱的并发症。虽然治疗策略历来侧重于减少胆固醇沉积,但最近的研究强调了炎症的关键作用。先天性炎症是导致斑块不稳定和破裂的重要原因,因此需要在疾病的各个阶段进行干预。大量研究强调了针对动脉粥样硬化中先天性免疫通路的治疗潜力,揭示了在了解动脉病变中炎症过程的分子机制方面取得的重大进展。值得注意的是,研究表明,通过靶向白细胞介素-1受体相关激酶(IRAK)和激活TNF受体相关因子6(TRAF6)(涉及收费样受体(TLRs)的信号通路),调节microRNA-146a(miR-146a)的表达可影响先天性炎症,有效阻止动脉粥样硬化的进展,并增强斑块的稳定性。了解其中错综复杂的机制至关重要。本研究全面分析了 miR-146a 发挥作用的证据和基本机制。将这些发现融入临床实践可能预示着管理动脉粥样硬化性心血管疾病的变革时代的到来。
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11.50
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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