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长链非编码 RNA SOX2-OT:在精神疾病、癌症和糖尿病并发症中的调控、功能和作用。

Long Noncoding RNA SOX2-OT: Regulations, Functions, and Roles on Mental Illnesses, Cancers, and Diabetic Complications.

机构信息

Department of General Medicine, The First Affiliated Hospital of Henan University of Science and Technology, Luoyang 471000, China.

Department of Public Health, School of Basic Medical Sciences, Henan University of Science and Technology, Luoyang 471000, China.

出版信息

Biomed Res Int. 2020 Nov 26;2020:2901589. doi: 10.1155/2020/2901589. eCollection 2020.

DOI:10.1155/2020/2901589
PMID:33294436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7718063/
Abstract

SRY-box transcription factor 2 (SOX2) overlapping transcript (SOX2-OT) is an evolutionarily conserved long noncoding RNA. Its intronic region contains the SOX2 gene, the major regulator of the pluripotency of embryonic stem cells. The human SOX2-OT gene comprises multiple exons and has multiple transcription start sites and generates hundreds of transcripts. Transcription factors (IRF4, AR, and SOX3), transcriptional inhibitors (NSPc1, MTA3, and YY1), and miRNAs (miR-211 and miR-375) have been demonstrated to control certain SOX2-OT transcript level at the transcriptional or posttranscriptional levels. Accumulated evidence indicates its crucial roles in the regulation of the SOX2 gene, miRNAs, and transcriptional process. Restricted expression of SOX2-OT transcripts in the brain results in the association between SOX2-OT single nucleotide polymorphisms and mental illnesses such as schizophrenia and anorexia nervosa. SOX2-OT is notably elevated in tumor tissues, and a high level of SOX2-OT is well correlated with poor clinical outcomes in cancer patients, leading to the establishment of its role as an oncogene and a prognostic or diagnostic biomarker for cancers. The emerging evidence supports that SOX2-OT mediates diabetic complications. In summary, SOX2-OT has diversified functions and could be a therapeutic target for various diseases.

摘要

性别决定区 Y 框转录因子 2(SOX2)重叠转录物(SOX2-OT)是一种进化上保守的长非编码 RNA。其内含子区域包含 SOX2 基因,SOX2 基因是胚胎干细胞多能性的主要调节因子。人类 SOX2-OT 基因包含多个外显子,具有多个转录起始位点,并产生数百种转录本。转录因子(IRF4、AR 和 SOX3)、转录抑制剂(NSPc1、MTA3 和 YY1)和 microRNAs(miR-211 和 miR-375)已被证明可以在转录或转录后水平控制某些 SOX2-OT 转录本的水平。越来越多的证据表明它在 SOX2 基因、microRNAs 和转录过程的调节中起着关键作用。SOX2-OT 转录本在大脑中的表达受限导致 SOX2-OT 单核苷酸多态性与精神疾病(如精神分裂症和神经性厌食症)之间存在关联。SOX2-OT 在肿瘤组织中显著升高,高水平的 SOX2-OT 与癌症患者的不良临床结局密切相关,这使其成为癌基因和癌症预后或诊断生物标志物的建立。新出现的证据支持 SOX2-OT 介导糖尿病并发症。总之,SOX2-OT 具有多样化的功能,可能成为各种疾病的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9fd/7718063/06f57ed86b1a/BMRI2020-2901589.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9fd/7718063/ea43f9c7df0c/BMRI2020-2901589.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9fd/7718063/06f57ed86b1a/BMRI2020-2901589.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9fd/7718063/ea43f9c7df0c/BMRI2020-2901589.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c9fd/7718063/06f57ed86b1a/BMRI2020-2901589.002.jpg

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Mol Cancer. 2020 Feb 4;19(1):25. doi: 10.1186/s12943-020-1143-7.
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