Evidence map›Paper›PMID 32051722›Full record

ArticleArchives of medical science : AMS2020

Aberrant expression of long non-coding RNAs (lncRNAs) is involved in brain glioma development.

Yi Ding, Xinfa Wang, Junchen Pan, Minjun Ji, Zhengxiang Luo, Penglai Zhao, Yansong Zhang, Gang Wang

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. PUMA mediated afatinib-induced apoptosis in glioma cells.Archives of medical science : AMS · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
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  8. Emerging Role of Non-coding RNAs in Autism Spectrum Disorder.Journal of molecular neuroscience : MN · 2022
    Review
  9. Article
  10. 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

8 authors at 2 institutions in 1 country.

Yi DingDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Xinfa WangDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Junchen PanDepartment of Neurosurgery, Nanjing BenQ hospital, Nanjing, China.
Minjun JiDepartment of Neurosurgery, Nanjing Medical University, Nanjing, China.
Zhengxiang LuoDepartment of Neurosurgery, Nanjing Brian Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Penglai ZhaoDepartment of Neurosurgery, Nanjing Brian Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Yansong ZhangDepartment of Neurosurgery, Nanjing Brian Hospital Affiliated to Nanjing Medical University, Nanjing, China.
Gang WangDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNSecond Affiliated Hospital of Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAberrant expression of long non-coding RNAs (lncRNAs) has been implicated in various diseases, including cancer. However, little is known about lncRNAs in human brain gliomas. MATERIAL AND

methodsWe examined lncRNA profiles from three glioma specimens using lncRNA expression profiling microarrays. Quantitative real-time RT-PCR was used to analyze the differential expression of raw intensities of lncRNA expression in glioma and peritumoral tissues.

resultsWe found 4858 lncRNAs to be differentially expressed between tumor tissue and peritumoral tissue. Of these, 2845 lncRNAs were up-regulated (fold change > 3.0) and 2013 were down-regulated (fold change < 1/3). A total of 4084 messenger RNAs were also differentially expressed, including 2280 up-regulated transcripts (fold change > 3.0) and 1804 that were down-regulated (fold change < 1/3). Consistent with the microarray data, qPCR confirmed differential expression of these 6 lncRNAs (ak125809, ak098473, uc002ehu.1, bc043564, NR_027322, and uc003qmb.2) between tumor and peritumoral tissue. We next established co-expression networks of differentially expressed lncRNAs and mRNAs. Many mRNAs, such as LOC729991, NUDCD1, SHC3, PDGFA, and MDM2, and lncRNAs, such as ENST00000425922, ENST00000455568, uc002ukz.1, ENST00000502715, and NR_027873, have been shown to play important roles in glioma development. Consistent with this, pathway analysis revealed that "GLIOMA" (KEGG Pathway ID: hsa05214) was significantly enriched in tumor tissue.

conclusionsOur data suggest that altered expression of lncRNAs may be a critical determinant of tumorigenesis in glioma patients.

Indexed as

gliomalncRNAsmicroarrays

Identifiers

PMID32051722
PMCPMC6963149
OpenAlexW2999548473

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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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 Socratic graph.