Evidence map›Paper›PMID 32059338›Full record

ArticleMolecular therapy. Nucleic acids2020

Identification of the Regulatory Role of lncRNA SNHG16 in Myasthenia Gravis by Constructing a Competing Endogenous RNA Network.

Jianjian Wang, Yuze Cao, Xiaoyu Lu, Xiaolong Wang, Xiaotong Kong, Chunrui Bo, Shuang Li, Ming Bai, Yang Jiao, Hongyu Gao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

26 citing papers in PubMed, 34 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Jianjian WangDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Yuze CaoDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.
Xiaoyu LuDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Xiaolong WangDepartment of Orthopedics, Harbin Medical University Cancer Hospital, Harbin 150000, China.
Xiaotong KongDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Chunrui BoDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Shuang LiDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Ming BaiDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Yang JiaoDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Hongyu GaoDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China.
Xiuhua YaoTianjin Neurosurgical Institute, Tianjin Key Laboratory of Cerebral Vascular and Neurodegenerative Diseases, Tianjin Huanhu Hospital, Tianjin 300350, China.
Shangwei NingCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China. Electronic address: ningsw@ems.hrbmu.edu.cn.
Lihua WangDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China. Electronic address: wanglh211@163.com.
Huixue ZhangDepartment of Neurology, The Second Affiliated Hospital of Harbin Medical University, Harbin 150081, China. Electronic address: zhanghuixue2009@163.com.
Second Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CNPeking Union Medical College Hospital · CNThird Affiliated Hospital of Harbin Medical University · CNTianjin Huanhu Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myasthenia gravis (MG) is an autoimmune disorder resulting from antibodies against the proteins at the neuromuscular junction. Emerging evidence indicates that long non-coding RNAs (lncRNAs), acting as competing endogenous RNAs (ceRNAs), are involved in various diseases. However, the regulatory mechanisms of ceRNAs underlying MG remain largely unknown. In this study, we constructed a lncRNA-mediated ceRNA network involved in MG using a multi-step computational strategy. Functional annotation analysis suggests that these lncRNAs may play crucial roles in the immunological mechanism underlying MG. Importantly, through manual literature mining, we found that lncRNA SNHG16 (small nucleolar RNA host gene 16), acting as a ceRNA, plays important roles in the immune processes. Further experiments showed that SNHG16 expression was upregulated in peripheral blood mononuclear cells (PBMCs) from MG patients compared to healthy controls. Luciferase reporter assays confirmed that SNHG16 is a target of the microRNA (miRNA) let-7c-5p. Subsequent experiments indicated that SNHG16 regulates the expression of the key MG gene interleukin (IL)-10 by sponging let-7c-5p in a ceRNA manner. Furthermore, functional assays showed that SNHG16 inhibits Jurkat cell apoptosis and promotes cell proliferation by sponging let-7c-5p. Our study will contribute to a deeper understanding of the regulatory mechanism of MG and will potentially provide new therapeutic targets for MG patients.

Indexed as

ceRNA networkIL-10let-7c-5pmyasthenia gravisSNHG16

Identifiers

PMID32059338
PMCPMC7016163
OpenAlexW2999814618

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.