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长链非编码RNA MALAT1在视网膜病变发生发展中的作用:综述

LncRNA MALAT1's role in the development of retinopathy: A review.

作者信息

Yang Gukun, Huang Xionggao

机构信息

Department of Ophthalmology, The First Affiliated Hospital of Hainan Medical University, Haikou, Hainan Province, PR China.

Key Laboratory of Emergency and Trauma of Ministry of Education, The First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, PR China.

出版信息

Medicine (Baltimore). 2025 Mar 21;104(12):e41954. doi: 10.1097/MD.0000000000041954.

Abstract

Long noncoding RNA (lncRNA) metastasis-associated lung adenocarcinoma transcript 1 (MALAT1) and retinopathy are 2 distinct yet interconnected areas of research in the field of ocular studies. MALAT1, with its diverse biological functions, has been extensively studied and demonstrated to play a role in various diseases, including ocular pathologies. Its involvement in alternative splicing regulation, transcriptional control, and the competing endogenous RNA (ceRNA) network suggests its potential implication in retinopathy. Retinopathy refers to a group of disorders that affect the retina, leading to vision impairment and, in severe cases, even blindness. These conditions include diabetic retinopathy, retinoblastoma, proliferative vitreoretinopathy, retinopathy of prematurity, and retinal neurodegeneration. The understanding of the molecular mechanisms underlying the development and progression of retinopathy, along with the potential involvement of MALAT1, can provide valuable insights for the diagnosis and treatment of this condition. Retinopathy, characterized by various manifestations and underlying mechanisms, presents a significant challenge in the field of ophthalmology. As a complex disease, its pathogenesis involves multifactorial factors, including angiogenic dysregulation, inflammatory responses, oxidative stress, and cellular signaling abnormalities. The emerging role of long noncoding RNA MALAT1 in retinopathy has attracted considerable attention. MALAT1 has been found to participate in multiple cellular processes, including alternative splicing regulation and transcriptional control. Additionally, the competing endogenous RNA (ceRNA) network involving MALAT1 indicates its potential relevance as a regulator in retinopathy. Further investigations into the specific mechanisms underlying MALAT1's involvement in retinopathy pathogenesis may provide valuable insights into the development of diagnostic and therapeutic approaches for managing retinal disorders.

摘要

长链非编码RNA(lncRNA)转移相关肺腺癌转录本1(MALAT1)与视网膜病变是眼科学领域两个不同但相互关联的研究领域。MALAT1具有多种生物学功能,已得到广泛研究,并被证明在包括眼部疾病在内的多种疾病中发挥作用。它参与可变剪接调控、转录控制以及竞争性内源RNA(ceRNA)网络,提示其在视网膜病变中可能具有潜在作用。视网膜病变是指一组影响视网膜的疾病,可导致视力损害,严重时甚至失明。这些病症包括糖尿病性视网膜病变、视网膜母细胞瘤、增殖性玻璃体视网膜病变、早产儿视网膜病变以及视网膜神经退行性变。了解视网膜病变发生发展的分子机制以及MALAT1的潜在参与情况,可为该病症的诊断和治疗提供有价值的见解。视网膜病变具有多种表现形式和潜在机制,在眼科领域构成了重大挑战。作为一种复杂疾病,其发病机制涉及多因素,包括血管生成失调、炎症反应、氧化应激和细胞信号异常。长链非编码RNA MALAT1在视网膜病变中新兴的作用已引起相当大的关注。已发现MALAT1参与多种细胞过程,包括可变剪接调控和转录控制。此外,涉及MALAT1的竞争性内源RNA(ceRNA)网络表明其作为视网膜病变调节因子的潜在相关性。进一步研究MALAT1参与视网膜病变发病机制的具体机制,可能为开发视网膜疾病的诊断和治疗方法提供有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5889/11936551/c932a148c1f4/medi-104-e41954-g001.jpg

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