Evidence map›Paper›PMID 32613482›Full record

ArticleMolecular and cellular biochemistry2020

LncRNA SNHG6 promotes LMO3 expression by sponging miR-543 in glioma.

Yin Zhang, Jiayin An, Yuchun Pei

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. LncRNA SNHG6 role in clinicopathological parameters in cancers.European journal of medical research · 2023
    Review
  4. LncRNA SNHG6 role in clinicopathological parameters in cancers.European journal of medical research · 2023
    Review
  5. Review
  6. Article
  7. Article
  8. Bioinformatics Profiling and Experimental Validation of 4 Differentially-Expressed LIM Genes in the Course of Colorectal-Adenoma-Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
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

3 authors at 2 institutions in 1 country.

Yin ZhangDepartment of Neurosurgery, Xinqiao Hospital, Army Medical University (Third Military Medical University), No. 9 City Garden West Road, Tianxing Bridge, Shapingba District, Chongqing, 400037, China. zhangyin6655@163.com.ORCID http://orcid.org/0000-0002-5676-7812
Jiayin AnDepartment of Neurosurgery, Eastern Theatre Naval Hospital of Chinese People's Liberation Army, Zhoushan, Zhejiang, China.
Yuchun PeiDepartment of Neurosurgery, Xinqiao Hospital, Army Medical University (Third Military Medical University), No. 9 City Garden West Road, Tianxing Bridge, Shapingba District, Chongqing, 400037, China.
Army Medical University · CNChinese People's Liberation Army · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small nucleolar RNA host gene 6 (SNHG6) was a newly discovered long non-coding RNA, which was involved in the occurrence and development of a variety of cancers and was on the rise in human cancers. However, the molecular mechanism of SNHG6 in glioma required further investigation. The levels of SNHG6, microRNA-543 (miR-543) and LIM-only protein 3 (LMO3) were detected in glioma tissues and cells by quantitative real-time polymerase chain reaction. We examined cell proliferation and apoptosis rate by methylthiazolyldiphenyl-tetrazolium bromide and flow cytometry assays, respectively. Transwell assay was used to measure cell migration and invasion. The target relationships were predicted by StarBase v.2.0 and TargetScan and confirmed by dual-luciferase reporter assay. Spearman's test was adopted for expression correlation of SNHG6, miR-543 and LMO3 in tissues. The protein expression level of LMO3 was assessed by western blot. We found that SNHG6 was obviously upregulated in glioma tissues and cells. SNHG6 knockdown significantly repressed glioma cell proliferation, migration and invasion, and induced apoptosis. Additionally, SNHG6 directly targeted miR-543 and their expression was negatively correlated in glioma tissues. And miR-543 targeted LMO3 and their expression was also inversely correlated. We found that silencing LMO3 also inhibited the progression of glioma cells. Importantly, SNHG6 could competitively sponging miR-543 thereby modulating LMO3 in glioma cells. SNHG6 served as an oncogene and played a vital role in glioma development through miR-543/LMO3 axis.

Indexed as

Gene Expression Regulation, NeoplasticAdaptor Proteins, Signal TransducingApoptosisBiomarkers, TumorCell ProliferationGliomaHumansLIM Domain ProteinsMicroRNAsPrognosisRNA, Long NoncodingTumor Cells, CulturedAdaptor Proteins, Signal TransducingBiomarkers, TumorLIM Domain ProteinsLMO3 protein, humanlong non-coding RNA SNHG6, humanMicroRNAsMIRN543 microRNA, humanRNA, Long NoncodingCell progressGliomaLMO3miR-543SNHG6

Identifiers

PMID32613482
OpenAlexW3038266171

What OpenQuestion holds

Textmetadata
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.