Evidence map›Paper›PMID 32280303›Full record

ArticleCancer cell international2020

CREB1-induced miR-1204 promoted malignant phenotype of glioblastoma through targeting NR3C2.

Xinli Zhao, Fazheng Shen, Jiwei Ma, Shupeng Zhao, Lei Meng, Xiangyang Wang, Shufeng Liang, Jianing Liang, Chaoshuai Hu, Xinzhong Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2020. 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
1.0field-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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
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  4. Protein and peptide letters · 2024
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  8. Mechanism of CREB1 in cardiac function of rats with heart failure via regulating the microRNA-376a-3p/TRAF6 axis.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Article
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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

10 authors at 1 institution in 1 country.

Xinli Zhao *Department of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Fazheng Shen *Department of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Jiwei MaDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Shupeng ZhaoDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Lei MengDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Xiangyang WangDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Shufeng LiangDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Jianing LiangDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Chaoshuai HuDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
Xinzhong ZhangDepartment of Neurosurgery, The First Affiliated Hospital of Xinxiang Medical University, 88 Health Road, Weihui, 453100 Henan China.
First Affiliated Hospital of Xinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioblastoma (GBM) is a subclass of brain malignancy with unsatisfactory prognosis. MicroRNAs (miRNAs) are a group of non-coding RNAs (ncRNAs) that exert key function on tumorigenesis and tumor development. PURPOSES: The purpose of this work was to unravel the biological behavior and mechanism of miR-1204 in GBM.

methodsExpressions of miR-1204, NR3C2 and CREB1 were detected by RT-qPCR and western blot. Proliferation and apoptosis of GBM cells were detected by CCK-8, colony formation, caspase-3 activity and TUNEL assays. Molecular interplays were examined by ChIP, RIP, and luciferase reporter assays.

resultsMiR-1204 level was elevated in GBM cell lines. Functionally, miR-1204 aggravated cell proliferation whereas suppressed cell apoptosis in GBM cells. Mechanistically, cAMP Responsive Element Binding Protein 1 (CREB1) bound to the promoter of miR-1204 and activated the transcription of miR-1204. Furthermore, miR-1204 targeted and inhibited Nuclear receptor subfamily 3 group C member 2 (NR3C2), a tumor suppressor gene in GBM cells. Rescue assays indicated that NR3C2 participated in the regulation of miR-1204 on the malignant phenotype of GBM cells.

conclusionsWe observed for the first time that CREB1-induced miR-1204 promoted malignant phenotype of GBM through targeting NR3C2, indicating that miR-1204 acted as a novel oncogenic miRNA in GBM.

Indexed as

CREB1GlioblastomamiR-1204NR3C2

Identifiers

PMID32280303
PMCPMC7137285
OpenAlexW3015330461

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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.