TGF-β:动脉粥样硬化的分子机制- SMAD通路的见解和基因治疗前景。

IF 3.5 4区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Klaudia Bonowicz, Dominika Jerka, Karolina Ławkowska, Jolanta Łuniewska-Bury, Irena Wrońska, Yidong Bai, Maciej Gagat
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引用次数: 0

摘要

动脉粥样硬化是全球发病率和死亡率的主要原因,其特点是纤维元素、脂质和动脉钙化积聚导致斑块形成,导致缺血性中风、冠状动脉疾病和心肌梗死等并发症。传统的治疗方法主要针对症状,但不能针对潜在的原因,这促使人们探索基因治疗等新方法。TGF-β家族包括TGF-β1、TGF-β2和TGF-β3,在细胞增殖、凋亡和迁移等过程中起关键作用,其失调与心血管疾病密切相关。在动脉粥样硬化中,TGF-β影响关键因素,如巨噬细胞胆固醇调节、斑块稳定性和血管平滑肌细胞功能,同时也有助于内皮功能障碍——疾病发展的早期阶段。个性化医疗强调了根据基因谱定制治疗的重要性,特别是针对TGF-β途径的变异,如TGF-β1和TGFBR2中的snp,这可以提供更精确的干预措施。CRISPR-Cas9和基于rna的疗法等新兴技术能够靶向调节这些遗传因素,为缓解疾病进展提供了新的途径。CRISPR-Cas9允许直接编辑与动脉粥样硬化相关的基因位点,潜在地纠正突变或调节表达水平,而基于rna的疗法,包括sirna和反义寡核苷酸,为解决失调基因提供了额外的精确工具。本文综述了TGF-β通路参与或调节的关键基因和其他分子,这些基因和分子可能作为基因治疗干预动脉粥样硬化和相关心血管疾病的精确靶点。通过靶向参与胆固醇代谢、炎症和内皮功能的基因,基因治疗提供了一种有针对性的策略来改善这些疾病的遗传驱动因素。总之,通过基因治疗调节TGF-β信号有可能彻底改变动脉粥样硬化和其他心血管疾病的治疗,同时揭示这些疾病的潜在遗传机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TGF-β: The Molecular Mechanisms of Atherosclerosis - insights into SMAD Pathways and Gene Therapy Prospects.

Atherosclerosis, a leading cause of global morbidity and mortality, is characterized by plaque formation resulting from the accumulation of fibrous elements, lipids, and calcification in arteries, leading to complications such as ischemic stroke, coronary artery disease, and myocardial infarction. Traditional treatments primarily address symptoms but fail to target underlying causes, prompting exploration of novel approaches like gene therapy. The TGF-β family, encompassing TGF-β1, TGF-β2, and TGF-β3, plays a critical role in cellular processes including proliferation, apoptosis, and migration, with its dysregulation strongly linked to cardiovascular diseases. In atherosclerosis, TGF-β influences key factors, such as macrophage cholesterol regulation, plaque stability, and vascular smooth muscle cell function, while also contributing to endothelial dysfunction- an early stage in disease development. Personalized medicine has highlighted the importance of tailoring therapies to genetic profiles, particularly regarding TGF-β pathway variations such as SNPs in TGF-β1 and TGFBR2, which could inform more precise interventions. Emerging technologies like CRISPR-Cas9 and RNA-based therapies enable targeted modulation of these genetic factors, offering new avenues to mitigate disease progression. CRISPR-Cas9 allows direct editing of gene loci linked to atherosclerosis, potentially correcting mutations or modulating expression levels, while RNA-based therapies, including siRNAs and antisense oligonucleotides, provide additional precision tools for addressing dysregulated genes. This review focuses on identifying key genes and additional molecular players involved in or regulated by the TGF-β pathway that may serve as precise targets for gene therapy intervention in atherosclerosis and related cardiovascular diseases. By targeting genes involved in cholesterol metabolism, inflammation, and endothelial function, gene therapy offers a targeted strategy to ameliorate the genetic drivers of these conditions. In summary, modulation of TGF-β signaling by gene therapy has the potential to revolutionize the treatment of atherosclerosis and other cardiovascular diseases while shedding light on the underlying genetic mechanisms of these disorders.

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来源期刊
Current medicinal chemistry
Current medicinal chemistry 医学-生化与分子生物学
CiteScore
8.60
自引率
2.40%
发文量
468
审稿时长
3 months
期刊介绍: Aims & Scope Current Medicinal Chemistry covers all the latest and outstanding developments in medicinal chemistry and rational drug design. Each issue contains a series of timely in-depth reviews and guest edited thematic issues written by leaders in the field covering a range of the current topics in medicinal chemistry. The journal also publishes reviews on recent patents. Current Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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