Evidence map›Paper›PMID 29480405›Full record

ArticleJournal of molecular histology2018

miR-484/MAP2/c-Myc-positive regulatory loop in glioma promotes tumor-initiating properties through ERK1/2 signaling.

Renhui Yi, Jiugeng Feng, Shaochun Yang, Xiaoyu Huang, Yuanyuan Liao, Zheng Hu, Muyun Luo

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular histology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed, 37 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Renhui YiGannan Medical University, Ganzhou, 341000, Jiangxi, People's Republic of China.
Jiugeng FengDepartment of Neurosurgery, the First Affiliated Hospital of Nanchang University, Nanchang, 330006, Jiangxi, People's Republic of China.
Shaochun YangDepartment of Neurosurgery, the First Affiliated Hospital of Gannan Medical University, No. 23 Youth Road, Ganzhou, 341000, Jiangxi, People's Republic of China. yangshch680709@hotmail.com.ORCID http://orcid.org/0000-0003-2172-8626
Xiaoyu HuangGannan Medical University, Ganzhou, 341000, Jiangxi, People's Republic of China.
Yuanyuan LiaoDepartment of Ultrasonography, the First Affiliated Hospital of Gannan Medical University, Ganzhou, 341000, Jiangxi, People's Republic of China.
Zheng HuDepartment of Neurosurgery, the First Affiliated Hospital of Gannan Medical University, No. 23 Youth Road, Ganzhou, 341000, Jiangxi, People's Republic of China.
Muyun LuoDepartment of Neurosurgery, the First Affiliated Hospital of Gannan Medical University, No. 23 Youth Road, Ganzhou, 341000, Jiangxi, People's Republic of China.
First Affiliated Hospital of Gannan Medical University · CNGannan Medical University · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioma is the most common intracranial malignant tumor. Cancer stem cells (CSCs) are resistant to chemotherapy and radiotherapy, and are closely related to cancer metastasis and recurrence. In this study, we aimed to explore the effect of miR-484 on glioma stemness and the underlying mechanism involved. miR-484 enhanced glioma tumor-initiating properties in vitro and in vivo. Moreover, miR-484 was shown to directly target MAP2, resulting in activation of ERK1/2 signaling and promotion of stemness in glioma. The ERK1/2 signaling facilitated the formation of a miR-484/MAP2/c-Myc positive feedback loop in glioma. High miR-484 expression predicted a poor prognosis for glioma patients, and high MAP2 expression predicted a good prognosis for glioma patients. Low miR-484 expression and high MAP2 expression was associated with the best prognosis in glioma. Our study suggests that miR-484 and MAP2 can be utilized as predictors for the clinical diagnosis and prognosis of glioma, and miR-484 and MAP2 are potential targets for the treatment of glioma.

Indexed as

MAP Kinase Signaling SystemCell Transformation, NeoplasticFeedback, PhysiologicalGliomaHumansMicroRNAsMicrotubule-Associated ProteinsPrognosisProto-Oncogene Proteins c-mycSignal TransductionTumor Cells, CulturedMAP2 protein, humanMicroRNAsMicrotubule-Associated ProteinsMIRN484 microRNA, humanMYC protein, humanProto-Oncogene Proteins c-mycc-MycGliomaMAP2MicroRNAsmiR-484Stemness

Identifiers

PMID29480405
OpenAlexW2790206514

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.