早幼粒细胞白血病蛋白:动脉粥样硬化抑制蛋白?

Cali B Corbett, Amanda K St Paul, Michael V Autieri
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引用次数: 0

摘要

动脉粥样硬化斑块中多达70%的细胞起源于血管平滑肌细胞(VSMC),而调节VSMC迁移、增殖和表型调节的途径和蛋白质为合理设计药物以减少动脉粥样硬化性血管疾病提供了新的靶点。在这一卷临床科学中,Karle等人证明肿瘤抑制因子早幼粒细胞白血病蛋白(PML)在VSMC表型调节和对炎症刺激的反应中起重要作用(临床科学(2021)135(7),887-905;DOI: 10.1042 / CS20201399)。这项重要的工作表明,PML,以前未被认为是动脉粥样硬化发展的参与者,可能代表抗动脉粥样硬化治疗方式的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Promyelocytic leukemia protein: an atherosclerosis suppressor protein?

As many as 70% of cells in atherosclerotic plaque are vascular smooth muscle cell (VSMC) in origin, and pathways and proteins which regulate VSMC migration, proliferation, and phenotype modulation represent novel targets for rational drug design to reduce atherosclerotic vascular disease. In this volume of Clinical Science, Karle et al. demonstrate that tumor suppressor, promyelocytic leukemia protein (PML) plays an important role in regulation of VSMC phenotype and response to inflammatory stimuli (Clin Sci (2021) 135(7), 887-905; DOI: 10.1042/CS20201399). This important work demonstrates that PML, previously unrecognized as a participant in development of atherosclerosis, may represent a novel target for anti-atherosclerotic therapeutic modalities.

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