Evidence map›Paper›PMID 31807002›Full record

ArticleOncoTargets and therapy2019

MicroRNA-769-5p Promotes The Growth Of Glioma Cells By Targeting Lysine Methyltransferase 2A.

Mingze Chang, Peng Yan, Bei Zhang, Gejuan Zhang, Juanhong Wang, Hanming Ge, Nannan Han, Chengxue Du, Wenzhen Shi, Ye Tian

RetractedErratum issuedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in OncoTargets and therapy, 2019. 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 It has been retracted, and should not be counted.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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 38% 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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. miR-381-3p Involves in Glioma Progression by Suppressing Tumor-Promoter Factor ANTXR1.Computational and mathematical methods in medicine · 2021
    Article
  8. MicroRNA-629-5p promotes osteosarcoma proliferation and migration by targeting caveolin 1.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2021
    Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Mingze ChangDepartment of Neurology, Xi'an No. 3 Hospital, Xi'an 710021, People's Republic of China.
Peng YanThe College of Life Sciences, Northwest University, Xi'an 710069, People's Republic of China.
Bei ZhangDepartment of Neurology, The First Affiliated Hospital of Xi'an Medical University, Xi'an 710077, People's Republic of China.
Gejuan ZhangDepartment of Neurology, Xi'an No. 3 Hospital, Xi'an 710021, People's Republic of China.
Juanhong WangDepartment of Pathology, Xi'an No.3 Hospital, Xi'an 710021, People's Republic of China.
Hanming GeDepartment of Neurology, Xi'an No. 3 Hospital, Xi'an 710021, People's Republic of China.
Nannan HanDepartment of Neurology, Xi'an No. 3 Hospital, Xi'an 710021, People's Republic of China.
Chengxue DuDepartment of Neurology, Xi'an No. 3 Hospital, Xi'an 710021, People's Republic of China.
Wenzhen ShiDepartment of Neurology, Xi'an No. 3 Hospital, Xi'an 710021, People's Republic of China.
Ye TianDepartment of Neurology, The Affiliated Hospital of Northwest University, Xi'an 710021, People's Republic of China.
Northwest University · CNXian Central Hospital · CNXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccumulating evidence supports the involvement of microRNAs (miRNAs) in the progression of human cancers including glioma. Recently, miR-769-5p has been reported to play a tumor suppressive role in colorectal cancer and lung cancer, whereas it exerts an oncogenic role in melanoma. However, the role of miR-769-5p and its related mechanism are poorly elucidated.

methodsThe levels of miR-769-5p in glioma tissues and adjacent non-tumor tissues were detected by qRT-PCR. In addition, the effects of miR-769-5p on cell proliferation and apoptosis were evaluated by CCK-8, EdU, colony formation and flow cytometric assays, respectively. Meanwhile, the dual-luciferase reporter assay was used to investigate the interaction of miR-769-5p and lysine methyltransferase 2A (KMT2A) in glioma.

resultsWe found that miR-769-5p expression was strongly upregulated in glioma tissues and cell lines. Glioma tissues with high World Health Organization (WHO) grades had obvious higher levels of miR-769-5p compared to samples with low WHO grades. Interestingly, glioma patients highly expressing miR-769-5p showed prominent poorer survivals. Knockdown of miR-769-5p significantly suppressed cell proliferation and resulted in apoptosis in glioma cells. Additionally, miR-769-5p silencing restrained in vivo growth of glioma cells in mice. Interestingly, KMT2A was identified to be a direct target of miR-769-5p in glioma cells. The expression of KMT2A mRNA was downregulated in glioma tissues and inversely correlated with miR-769-5p level. KMT2A overexpression inhibited cell proliferation and induced the apoptosis of A172 cells. Moreover, siRNA-mediated KMT2A silencing could partially abolish miR-769-5p knockdown-induced suppressive effects on A172 cells.

conclusionIn summary, our findings suggest that targeting miR-769-5p/KMT2A axis may be a promising therapeutic target for glioma treatment.

Indexed as

apoptosisgliomaKMT2AmiR-769-5ptumor growth

Identifiers

PMID31807002
PMCPMC6842300
OpenAlexW2987161714

What OpenQuestion holds

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Registered trials

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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.