Evidence map›Paper›PMID 28912531›Full record

ArticleScientific reports2017

TGF-â1-induced miR-503 controls cell growth and apoptosis by targeting PDCD4 in glioblastoma cells.

Pin Guo, Yanan Yu, Huanting Li, Daoxiang Zhang, Anjing Gong, Shifang Li, Wei Liu, Lei Cheng, Yongming Qiu, Weicheng Yao and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.4field-weighted citation impact, top 40% 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, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Pin GuoDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Yanan YuDepartment of Gastroenterology, the Affiliated Hospital of Qingdao University, Qingdao, China.
Huanting LiDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Daoxiang ZhangDivision of Oncology, Department of Internal Medicine, Washington University School of Medicine, Saint Louis, MO, 63110, USA.
Anjing GongDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Shifang LiDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Wei LiuDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Lei ChengDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Yongming QiuDepartment of Neurosurgery, South Campus, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Weicheng YaoDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China.
Luo LiDepartment of Neurology, Qingdao Municipal Hospital, Qingdao University, Qingdao, China. liluodoctor@163.com.
Yugong FengDepartment of Neurosurgery, the Affiliated Hospital of Qingdao University, Qingdao, China. fengyugong001@163.com.
Affiliated Hospital of Qingdao University · CNQingdao University · CNRenji Hospital · CNWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of microRNAs hae been shown to be closely associated with glioblastoma cell proliferation, apoptosis and drug resistance. However, mechanisms underlying the role of mcroRNAs in glioblastoma cell growth and apoptosis are not fully understood. In this study, we report that miR-503 is overexpressed in glioblastoma tissue compared with normal human brain tissue. Mechanistically, miR-503 can be induced by TGF-â1 at the transcriptional level by binding the smad2/3 binding elements in the promoter. Ectopic overexpression of miR-503 promotes cell growth and inhibits apoptosis by targeting PDCD4. In contrast, inhibition of miR-503 reduces cell growth. Furthermore, miR-503 inhibitor augments the growth inhibitory effect of temozolomide in glioblastoma cells. These results establish miR-503 as a promising molecular target for glioblastoma therapy.

Indexed as

Gene Expression Regulation, Neoplastic3' Untranslated RegionsApoptosisApoptosis Regulatory ProteinsCell Line, TumorCell ProliferationGene ExpressionGenes, ReporterGlioblastomaHumansMicroRNAsRNA-Binding ProteinsRNA InterferenceTransforming Growth Factor alpha3' Untranslated RegionsApoptosis Regulatory ProteinsMicroRNAsMIRN503 microRNA, humanPDCD4 protein, humanRNA-Binding ProteinsTransforming Growth Factor alpha

Identifiers

PMID28912531
PMCPMC5599596
OpenAlexW2755130672

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.