靶向MAPK信号在老年性黄斑变性中的作用

Ophthalmology and eye diseases Pub Date : 2016-06-23 eCollection Date: 2016-01-01 DOI:10.4137/OED.S32200
Svetlana V Kyosseva
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引用次数: 51

摘要

年龄相关性黄斑变性(AMD)是影响世界老年人不可逆失明的主要原因。AMD是一种复杂的多因素疾病,与人口统计学、遗传学和环境风险因素有关。氧化应激、炎症和细胞凋亡在AMD的发病机制中起着重要作用。丝裂原活化蛋白激酶(MAPK)信号通路可被多种细胞外刺激激活,包括生长因子、丝裂原、激素、细胞因子和不同的细胞应激源,如氧化应激。它们调节细胞增殖、分化、存活和凋亡。本文综述了人类和动物研究中关于MAPK信号与AMD关系的新发现。特异性MAPK抑制剂的使用可能是治疗这种使人衰弱的眼病的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Targeting MAPK Signaling in Age-Related Macular Degeneration.

Age-related macular degeneration (AMD) is a major cause of irreversible blindness affecting elderly people in the world. AMD is a complex multifactorial disease associated with demographic, genetics, and environmental risk factors. It is well established that oxidative stress, inflammation, and apoptosis play critical roles in the pathogenesis of AMD. The mitogen-activated protein kinase (MAPK) signaling pathways are activated by diverse extracellular stimuli, including growth factors, mitogens, hormones, cytokines, and different cellular stressors such as oxidative stress. They regulate cell proliferation, differentiation, survival, and apoptosis. This review addresses the novel findings from human and animal studies on the relationship of MAPK signaling with AMD. The use of specific MAPK inhibitors may represent a potential therapeutic target for the treatment of this debilitating eye disease.

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