Evidence map›Paper›PMID 29152664›Full record

ArticleMolecular medicine reports2017

Tumor suppressive role of miR-194-5p in glioblastoma multiforme.

Zhao Zhang, Bo Lei, Honggang Wu, Xiaoli Zhang, Niandong Zheng

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2017. 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
1.1field-weighted citation impact, top 26% 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, 24 citations in OpenAlex.

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  6. Recent advances of the regulation roles of MicroRNA in glioblastoma.International journal of clinical oncology · 2020
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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

5 authors at 1 institution in 1 country.

Zhao ZhangDepartment of Neurosurgery, The People's Hospital of Leshan City, Leshan, Sichuan 614000, P.R. China.
Bo LeiDepartment of Neurosurgery, The People's Hospital of Leshan City, Leshan, Sichuan 614000, P.R. China.
Honggang WuDepartment of Neurosurgery, The People's Hospital of Leshan City, Leshan, Sichuan 614000, P.R. China.
Xiaoli ZhangDepartment of Neurosurgery, The People's Hospital of Leshan City, Leshan, Sichuan 614000, P.R. China.
Niandong ZhengDepartment of Neurosurgery, The People's Hospital of Leshan City, Leshan, Sichuan 614000, P.R. China.
People's Hospital of Bishan District · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is defined by the World Health Organization as the most aggressive form of grade IV glioma, characterized by unrestrained cellular proliferation. microRNAs (miRs) serve important roles in the pathogenesis of GBM. However, the function of miR‑194‑5p in GBM remains unknown. In the present study, the miR‑194‑5p levels in GBM tissues and cells were evaluated using the reverse transcription‑quantitative polymerase chain reaction. Cellular proliferation was tested by MTT analysis. Cellular apoptosis was analyzed by fluorescence‑activated cell sorting. The protein level of insulin‑like growth factor 1 receptor, the target gene of miR‑194‑5p, was evaluated by western blotting. The interaction between miR‑194‑5p and the target gene was confirmed by the dual‑luciferase reporter assay. It was demonstrated that miR‑194‑5p inhibited cell growth and promoted apoptosis. In conclusion, the results of the present study indicated the tumor suppressive role of miR‑194‑5p.

Indexed as

ApoptosisCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorGlioblastomaHumansMaleMicroRNAsMicroRNAsMIRN194 microRNA, human

Identifiers

PMID29152664
PMCPMC5779985
OpenAlexW2765678916

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.