Identification and characterization of proliferative retinopathy-related long noncoding RNAs

被引:51
|
作者
Zhou, Rong-Mei [1 ,2 ]
Wang, Xiao-Quri [1 ,2 ]
Yao, Jin [1 ,2 ]
Shen, Yi [1 ]
Chen, Sai-Nan [1 ]
Yang, Hong [1 ,2 ]
Jiang, Qin [1 ,2 ,3 ]
Yan, Biao [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Hosp Eye, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Sch Clin Med 4, Nanjing 210029, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Inst Integrated Med, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
LncRNA; MALAT1; PVR; RPE; Peripheral blood; VITREORETINOPATHY; CANCER; CLASSIFICATION; MALAT1;
D O I
10.1016/j.bbrc.2015.07.120
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proliferative vitreoretinopathy (PVR) is a serious complication of retinal detachment and vitreoretinal surgery, which can lead to severe vision reduction. Long non-coding RNAs (lncRNAs) play critical roles in many biological processes and disease development. We attempted to determine the role of IncRNAs in the setting of PVR. Microarray analysis revealed that 78 lncRNAs were abnormally expressed in the epiretinal membranes (ERMs) of PVR patients, including 48 up-regulated and 30 down-regulated IncRNA transcripts. We subsequently focus on one IncRNA, MALAT1, and investigated its expression pattern in the biofluid of PVR patients. MALAT1 was significantly up-regulated in the cellular and plasma fraction of peripheral blood in PVR patients. MALAT1 expression was obviously reduced after PVR operation. In vitro experiments revealed the role of MALAT1 in regulating RPE proliferation and migration, which is critical for ERMs formation. This study suggests that IncRNAs are the potential regulators of PVR pathology. MALAT1 is a potential prognostic indicator and a target for the diagnosis and gene therapy for PVR diseases. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:324 / 330
页数:7
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