lncRNA: a promising target for cataracts

Author:

dong xiaoming1,liu yuxuan2,ji liyang3,wang jing4,zhang jisong3

Affiliation:

1. Cataract and Intraocular Lens Institute, Shenyang Aier Excellent Eye Hospital, Shenyang 110000, Liaoning Province, China,

2. Shenyang Aier Excellent Eye Hospital, Shenyang 110000, Liaoning Province, China,

3. Department of Ophthalmology, the Fourth Affiliated Hospital of China Medical University, Eye Hospital of China Medical University, Key Laboratory of Lens Research of Liaoning Province, Shenyang, China

4. Aier School of Ophthalmology, Central South University, Changsha 410000, Hunan Province, China,

Abstract

Abstract Long noncoding RNAs (lncRNAs) are nonprotein-coding transcripts containing >200 nucleotides. lncRNA was first considered the “noise” of genome transcription and had no biological function. With the deepening of research, lncRNA has been found to regulate gene expression at epigenetic, transcriptional, and translation levels, thus affecting cell proliferation, apoptosis, viability, immune response, and oxidative stress. More and more studies have shown that the expression and function of lncRNA are closely related to ophthalmic diseases, such as cataracts, glaucoma, and diabetic retinopathy. This review summarized the classification and mechanism of known lncRNAs and the role of lncRNAs in eye diseases, especially in cataracts, and further clarified their mechanism.

Publisher

Research Square Platform LLC

Reference99 articles.

1. Global prevalence and causes of visual impairment with special reference to the general population of Saudi Arabia;Alswailmi FK;Pakistan journal of medical sciences,2018

2. S. McCusker, M.M. Koola, Association of Ophthalmologic Disorders and Depression in the Elderly: A Review of the Literature, The primary care companion for CNS disorders 17(4) (2015).

3. RB1 gene mutations in Argentine retinoblastoma patients. Implications for genetic counseling;Parma D;PloS one,2017

4. Spectrum of RB1 mutations identified in 403 retinoblastoma patients;Price EA;Journal of medical genetics,2014

5. Frequent and Yet Unreported GNAQ and GNA11 Mutations are Found in Uveal Melanomas;Schneider B;Pathology oncology research: POR,2019

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3