Evidence map›Paper›PMID 28277190›Full record

ArticleOncology research2017

miR-422a Inhibits Glioma Proliferation and Invasion by Targeting IGF1 and IGF1R.

Haiyang Wang, Chongyang Tang, Meng Na, Wei Ma, Zhenfeng Jiang, Yifei Gu, Guizhen Ma, Haitao Ge, Hong Shen, Zhiguo Lin

Open access · hybridAbstract read
In one paragraph

Article in Oncology research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.8field-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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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  20. Circular RNAs and human glioma.Cancer biology & medicine · 2019
    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

10 authors at 2 institutions in 1 country.

Haiyang WangDepartment of Neurosurgery, The First Affiliated Hospital of Harbin Medical University, Harbin, P.R. China.
Chongyang Tang
Meng Na
Wei Ma
Zhenfeng Jiang
Yifei Gu
Guizhen Ma
Haitao Ge
Hong Shen
Zhiguo Lin
First Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is a common type of malignant brain tumor characterized by aggressive metastasis capability. Recent evidence has suggested that noncoding RNAs, including microRNAs, have important functions in the pathophysiology of glioma development. In this study, we investigated the biological function of miR-422a in human glioma. We found that miR-422a was downregulated in glioma tissues. We also demonstrated that expression of miR-422a in glioma cells markedly suppressed cell proliferation, migration, and invasion. In addition, we identified insulin-like growth factor 1 (IGF1) and IGF1 receptor (IGF1R) as inhibitory targets of miR-422a in glioma cells. We established that the expression levels of miR-422a were negatively correlated with the expression levels of IGF1/IGF1R and the clinical parameters in glioma patients. An IGFR inhibitor, AG1024, completely blocked the activity of miR-442a on glioma cell proliferation and invasion, which further confirmed that miR-422a functions through IGF1 and IGF1R.

Indexed as

Gene TargetingBrain NeoplasmsCell Line, TumorCell ProliferationGliomaHumansInsulin-Like Growth Factor IMicroRNAsNeoplasm InvasivenessReceptor, IGF Type 1Receptors, SomatomedinIGF1 protein, humanIGF1R protein, humanInsulin-Like Growth Factor IMicroRNAsMIRN422 microRNA, humanReceptor, IGF Type 1Receptors, Somatomedin

Identifiers

PMID28277190
PMCPMC7840806
OpenAlexW2592451187

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.