Evidence map›Paper›PMID 37066523›Full record

ArticleCNS neuroscience & therapeutics2023

U3 snoRNA-mediated degradation of ZBTB7A regulates aerobic glycolysis in isocitrate dehydrogenase 1 wild-type glioblastoma cells.

Weiwei Dong, Yunhui Liu, Ping Wang, Xuelei Ruan, Libo Liu, Yixue Xue, Teng Ma, Tiange E, Di Wang, Chunqing Yang and 3 more

Open access · goldAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Selective remodeling of snoRNA and sdRNA biology in glioblastoma.Frontiers in cell and developmental biology · 2026
    Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. SnoRNAs: The promising targets for anti-tumor therapy.Journal of pharmaceutical analysis · 2024
    Review
  10. SNORD3A Regulates STING Transcription to Promote Ferroptosis in Acute Kidney Injury.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  11. Article
  12. Article
  13. 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

13 authors at 3 institutions in 1 country.

Weiwei DongDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Yunhui LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Ping WangDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Xuelei RuanDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Libo LiuDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Yixue XueDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Teng MaDepartment of Neurobiology, School of Life Sciences, China Medical University, Shenyang, China.
Tiange EDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Di WangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Chunqing YangDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Hongda LinDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Jian SongDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
Xiaobai LiuDepartment of Neurosurgery, Shengjing Hospital of China Medical University, Shenyang, China.
China Medical University · CNLiaoning University · CNShenyang Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe isocitrate dehydrogenase (IDH) phenotype is associated with reprogrammed energy metabolism in glioblastoma (GBM) cells. Small nucleolar RNAs (snoRNAs) are known to exert an important regulatory role in the energy metabolism of tumor cells. The purpose of this study was to investigate the role of C/D box snoRNA U3 and transcription factor zinc finger and BTB domain-containing 7A (ZBTB7A) in the regulation of aerobic glycolysis and the proliferative capacity of IDH1 wild-type (IDH1

methodsQuantitative reverse transcription PCR and western blot assays were utilized to detect snoRNA U3 and ZBTB7A expression. U3 promoter methylation status was analyzed via bisulfite sequencing and methylation-specific PCR. Seahorse XF glycolysis stress assays, lactate production and glucose consumption measurement assays, and cell viability assays were utilized to detect glycolysis and proliferation of IDH1

resultsWe found that hypomethylation of the CpG island in the promoter region of U3 led to the upregulation of U3 expression in IDH1

conclusionU3 enhances aerobic glycolysis and proliferation in IDH1

Indexed as

GlioblastomaCell Line, TumorCell ProliferationDNA-Binding ProteinsGene Expression Regulation, NeoplasticGlycolysisHumansIsocitrate DehydrogenaseRNA, Small NucleolarTranscription FactorsDNA-Binding ProteinsIsocitrate DehydrogenaseRNA, Small NucleolarRNA, U3 small nucleolarTranscription FactorsZBTB7A protein, humanaerobic glycolysisglioblastomaIDH1U3ZBTB7A

Identifiers

PMID37066523
PMCPMC10493654
OpenAlexW4366084047

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.