Inhibition of endothelial cell proliferation as a potential therapeutic approach in hereditary hemorrhagic telangectasia

IF 9.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Nature cardiovascular research Pub Date : 2024-11-01 DOI:10.1038/s44161-024-00557-2
Nicolas Ricard, Sabine Bailly
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Abstract

Arteriovenous malformations are the hallmark of patients with hereditary hemorrhagic telangectasia. Research now finds that this could be due to endothelial cell-cycle acceleration via CDK6. These results could suggest repurposing CDK6 inhibitors for this disorder.

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将抑制内皮细胞增殖作为遗传性出血性毛细血管扩张症的一种潜在治疗方法。
动静脉畸形是遗传性出血性毛细血管扩张症患者的特征。现在的研究发现,这可能是由于内皮细胞周期通过CDK6加速所致。这些结果表明,CDK6抑制剂可以重新用于治疗这种疾病。
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