Evidence map›Paper›PMID 35012429›Full record

ArticleBioengineered2022

N(6)-adenosine-methyltransferase-14 promotes glioma tumorigenesis by repressing argininosuccinate synthase 1 expression in an m6A-dependent manner.

You-Qing Miao, Wei Chen, Jianfeng Zhou, Qiyang Shen, Ying Sun, Tao Li, Sheng-Chan Wang

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Bioengineered, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 17 citations in OpenAlex.

  1. Cross-talk of mFrontiers in immunology · 2025
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  6. The Critical Role of RNA mCellular and molecular neurobiology · 2023
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  8. YTHDF1 Attenuates TBI-Induced Brain-Gut Axis Dysfunction in Mice.International journal of molecular sciences · 2023
    Article
  9. Review
  10. Review
  11. Review
  12. The Potential Role of mAntioxidants (Basel, Switzerland) · 2022
    Review
  13. The Roles and Regulation of mBiomedicines · 2022
    Review
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

You-Qing MiaoDepartment of Neurosurgery, Nanjing Drum Tower Hospital, Nanjing, China.
Wei ChenDepartment of Urology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Jianfeng ZhouDepartment of Pediatric Surgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Qiyang ShenDepartment of Pediatric Surgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Ying SunDepartment of Neurosurgery, Nanjing Drum Tower Hospital, Nanjing, China.
Tao LiDepartment of Pediatric Surgery, Children's Hospital of Nanjing Medical University, Nanjing, China.
Sheng-Chan WangDepartment of Geriatrics, Geriatric Hospital of Nanjing Medical University, Nanjing, China.
Second Affiliated Hospital of Nanjing Medical University · CNNanjing Drum Tower Hospital · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is one of the leading causes of tumor-related deaths worldwide, but its potential mechanism remains unclear. This study aimed to explore the biological role and potential mechanism of argininosuccinate synthase 1 (ASS1) in glioma. The relative expression levels of ASS1 in glioma specimens and cell lines were calculated by quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and Western blotting. The biological functions of ASS1 were demonstrated using the 5-ethynyl-2'-deoxyuridine (EdU) assay, transwell assay, and in vivo experiments. In addition, methylated RNA immunoprecipitation (MeRIP), RNA immunoprecipitation (RIP), and luciferase reporter assays were performed to explore the molecular mechanism of ASS1 in glioma. ASS1 expression levels were found to be downregulated in glioma specimens and cell lines. Functionally, we confirmed that ASS1 inhibited glioma cell proliferation, migration, invasion, and growth both. Furthermore, we found that ASS1 was a target of N(6)-adenosine-methyltransferase-14 (METTL14)-mediated N

Indexed as

AdenosineAnimalsArgininosuccinate SynthaseBrain NeoplasmsCase-Control StudiesCell Line, TumorCell MovementCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticGliomaHumansMaleMethyltransferasesMiceNeoplasm TransplantationAdenosineArgininosuccinate SynthaseMethyltransferasesMETTL14 protein, humanN-methyladenosineRNA-Binding ProteinsYTHDF2 protein, humanASS1gliomamalignant progressionMETTL14N6-methyladenosine

Identifiers

PMID35012429
PMCPMC8805915
OpenAlexW4206139010

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.