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HMG-CoA还原酶途径、他汀类药物与血管保护作用

The HMG-CoA reductase pathway, statins and angioprevention.

作者信息

Feng Chong, Han Anjia, Ye Caisheng, Xu Rui, Li Mengfeng

机构信息

Sun Yat-sen University School of Medicine, Guangzhou GD, PRC.

出版信息

Semin Ophthalmol. 2006 Jan-Mar;21(1):29-35. doi: 10.1080/08820530500509382.

Abstract

Angiogenesis is one of the earliest and essential phenotypes acquired by tumors during carcinogenesis and thus might be a potential target for chemoprevention. Key to developing antiangiogenic chemoprevention is to identify new molecular targets and effective angiogenesis inhibitors. HMG-CoA reductase inhibitors, or statins, were originally designed to reduce cholesterol biosynthesis and have been extensively used as prevention drugs against hyperlipidemia and cardiovascular conditions. Recent research has found that statins promote endothelial death and inhibit experimental angiogenesis induced by growth factors or tumor, laying a foundation for developing statin-based angiopreventive strategies. This article reviews the biological effects of statins on endothelial cells and angiogenesis, possible underlying mechanisms and perspectives on future application of statins in preventing pathological angiogenesis.

摘要

血管生成是肿瘤在致癌过程中最早获得的重要表型之一,因此可能是化学预防的潜在靶点。开发抗血管生成化学预防的关键在于识别新的分子靶点和有效的血管生成抑制剂。HMG-CoA还原酶抑制剂,即他汀类药物,最初旨在降低胆固醇生物合成,并已广泛用作预防高脂血症和心血管疾病的药物。最近的研究发现,他汀类药物可促进内皮细胞死亡,并抑制生长因子或肿瘤诱导的实验性血管生成,为开发基于他汀类药物的血管预防策略奠定了基础。本文综述了他汀类药物对内皮细胞和血管生成的生物学效应、可能的潜在机制以及他汀类药物在预防病理性血管生成方面未来应用的前景。

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