Evidence map›Paper›PMID 22709411›Full record

ArticleCNS neuroscience & therapeutics2012

MiR-21 modulates hTERT through a STAT3-dependent manner on glioblastoma cell growth.

Ying-Yi Wang, Guan Sun, Hui Luo, Xie-Feng Wang, Feng-Ming Lan, Xiao Yue, Lin-Shan Fu, Pei-Yu Pu, Chun-Sheng Kang, Ning Liu and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 9% 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

52 citing papers in PubMed, 2 syntheses or guidelines pooled it, 78 citations in OpenAlex.

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  10. CRISPR-Cas knockout of miR21 reduces glioma growth.Molecular therapy oncolytics · 2022
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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

11 authors at 3 institutions in 1 country.

Ying-Yi WangDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, China.
Guan Sun
Hui Luo
Xie-Feng Wang
Feng-Ming Lan
Xiao Yue
Lin-Shan Fu
Pei-Yu Pu
Chun-Sheng Kang
Ning Liu
Yong-Ping You
Jiangsu Province Hospital · CNTianjin Medical University General Hospital · CNNantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeAs an important oncogenic miRNA, miR-21 has been reported to play crucial roles in glioblastoma (GBM) carcinogenesis. However, the precise biological function and molecular mechanism of miR-21 in GBM remain elusive. This study is designed to explore the mechanism of miR-21 involved in the control of GBM cell growth. METHODS AND

resultsMTT assay, cell cycle analysis, and apoptosis analysis showed that reduction of miR-21 inhibited cell growth in U87 and LN229 GBM cells. Further, reduction of miR-21 decreased the expression of human telomerase reverse transcriptase (hTERT) and repressed STAT3 expression and STAT3 phosphorylation. STAT3 inhibition led to a remarkable depletion of hTERT at both mRNA and protein levels by binding to the hTERT gene promoter by performing luciferase reporter assay and chromatin Immunoprecipitation PCR. Finally, knockdown of miR-21 considerably inhibited tumor growth and diminished the expression of STAT3 and hTERT in xenograft model.

conclusionOur findings indicate that miR-21 regulates hTERT expression mediated by STAT3, therefore controlling GBM cell growth.

Indexed as

Brain NeoplasmsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticGlioblastomaHumansMicroRNAsSTAT3 Transcription FactorTelomeraseMicroRNAsMIRN21 microRNA, humanSTAT3 protein, humanSTAT3 Transcription FactorTelomerase

Identifiers

PMID22709411
PMCPMC6493453
OpenAlexW1991892635

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.