Evidence map›Paper›PMID 30972186›Full record

ArticleAmerican journal of translational research2019

MicroRNA-524 inhibits the progress of glioma via the direct targeting of NCF2.

Tuoye Xu, Wan Yu, Qingquan Li, Xiaojian Li, Yan Shi, Boqiang Cao, Yaxuan Zhang, Seng Wang, Yan Zhang, Tianlu Wang and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2019. 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
1.7field-weighted citation impact, top 17% 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, 26 citations in OpenAlex.

  1. Annexin A2: regulating glioma's fate and a potential therapeutic target.Medical oncology (Northwood, London, England) · 2025
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Roles of Cadherin2 in Thyroid Cancer.Frontiers in oncology · 2022
    Article
  8. 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

11 authors at 2 institutions in 1 country.

Tuoye XuDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Wan YuDepartment of Neurosurgery, Affiliated Hospital of Integrated Traditional Chinese and Western Medicine, Nanjing University of Chinese Medicine Nanjing, Jiangsu Province, China.
Qingquan LiDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Xiaojian LiDepartment of Neurosurgery, Nanjing First Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Yan ShiDepartment of Neurosurgery, Nanjing First Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Boqiang CaoDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Yaxuan ZhangDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Seng WangDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Yan ZhangDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Tianlu WangDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Baosheng HuangDepartment of Neurosurgery, Sir Run Run Hospital, Nanjing Medical University Nanjing, Jiangsu Province, China.
Nanjing Medical University · CNNanjing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, a large amount of research has reported that microRNA (miRNA) dysregulation is closely related to glioma progression. miR-524, a member of the miRNA family, has been confirmed to be involved in many human diseases, including glioma. However, the role and molecular mechanism of miR-524 in glioma have not been clarified. In our study, we showed that miR-524 expression was significantly decreased in glioma and was associated with glioma recurrence. Next, we performed a series of assays and confirmed that the upregulation of miR-524 suppressed glucose uptake, proliferation, migration and invasion in glioma cell lines. Then, through bioinformatics software and a dual luciferase assay, we demonstrated that NCF2 was a target gene of miR-524. In addition, we found that NCF2 reintroduction restored the inhibitor effect of miR-524 on glioma progression. These results elucidate the mechanism of miR-524 in glioma development and provide a potential therapeutic strategy for glioma patients.

Indexed as

gliomaglucose uptakemiR-524NCF2

Identifiers

PMID30972186
PMCPMC6456563
OpenAlexW2990302056

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.