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microRNAs调控年龄相关性黄斑变性发病机制的研究进展
作者:谢丽蓉1 2  尹莉莉1 2 
单位:1. 上海交通大学附属第一人民医院 眼科, 上海 200080;
2. 上海市眼底病重点实验室, 上海 200080
关键词:年龄相关性黄斑变性 microRNA 氧化应激 新生血管 分子机制 
分类号:R774.5
出版年·卷·期(页码):2023·51·第一期(131-134)
摘要:

年龄相关性黄斑变性(age related macular degeneration,AMD),是发达国家65岁以上人群致盲的首要因素,在发展中国家的发病率也逐渐上升,然而其发病机制目前仍不明确。AMD的发病主要与衰老、氧化损伤、免疫炎症及新生血管生成等密切相关。microRNAs是一类编码长度约为22个核苷酸的非编码RNA,作为调节目的基因的重要分子,涉及细胞增殖、凋亡、代谢等多种活动,在阐明疾病的发病机制方面具有强大潜力。本文就近年来microRNAs在AMD的发生、发展阶段的调控机制进行综述。

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