Evidence map›Paper›PMID 18591254›Full record

ArticleMolecular and cellular biology2008

MicroRNA 21 promotes glioma invasion by targeting matrix metalloproteinase regulators.

Galina Gabriely, Thomas Wurdinger, Santosh Kesari, Christine C Esau, Julja Burchard, Peter S Linsley, Anna M Krichevsky

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 449 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
449citing papers in PubMed, 5 pooled it
24.3field-weighted citation impact, top 1% 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

449 citing papers in PubMed, 5 syntheses or guidelines pooled it, 884 citations in OpenAlex.

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  18. Nuclear Roles of Spliceosome-Associated microRNAs in Neuronal Cancer Cells.International journal of molecular sciences · 2025
    Article
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389 more citing papers are in PubMed but not listed here.

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 6 institutions in 2 countries.

Galina GabrielyCenter of Neurologic Diseases, Brigham and Women's Hospital, 4 Blackfan Circle, HIM 758, Boston, MA 02115, USA.
Thomas Wurdinger
Santosh Kesari
Christine C Esau
Julja Burchard
Peter S Linsley
Anna M Krichevsky
Rosetta Stone (United States) · USAmsterdam UMC Location VUmc · NLBrigham and Women's Hospital · USCenter for Neuro-Oncology · USHarvard University · USMassachusetts General Hospital · US

Funding

StatisticsP50CA086355 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI WEISSLEDER, MD, PHD, RALPH · 2000 to 2015
$27.8M
Targeting miRNA in brain tumors.R21CA116141 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI KRICHEVSKY, ANNA M. · 2005 to 2006
$297k
NCI NIH HHS P50 CA086355NCI NIH HHS P50 CA86355-04NCI NIH HHS R21 CA116141NCI NIH HHS R21CA116141
6 · The paper itself

Abstract

Substantial data indicate that microRNA 21 (miR-21) is significantly elevated in glioblastoma (GBM) and in many other tumors of various origins. This microRNA has been implicated in various aspects of carcinogenesis, including cellular proliferation, apoptosis, and migration. We demonstrate that miR-21 regulates multiple genes associated with glioma cell apoptosis, migration, and invasiveness, including the RECK and TIMP3 genes, which are suppressors of malignancy and inhibitors of matrix metalloproteinases (MMPs). Specific inhibition of miR-21 with antisense oligonucleotides leads to elevated levels of RECK and TIMP3 and therefore reduces MMP activities in vitro and in a human model of gliomas in nude mice. Moreover, downregulation of miR-21 in glioma cells leads to decreases of their migratory and invasion abilities. Our data suggest that miR-21 contributes to glioma malignancy by downregulation of MMP inhibitors, which leads to activation of MMPs, thus promoting invasiveness of cancer cells. Our results also indicate that inhibition of a single oncomir, like miR-21, with specific antisense molecules can provide a novel therapeutic approach for "physiological" modulation of multiple proteins whose expression is deregulated in cancer.

Indexed as

AnimalsApoptosisBase SequenceCell Line, TumorCell MovementDisease ProgressionDown-RegulationEnzyme InhibitorsExtracellular MatrixGene Expression ProfilingGene Expression Regulation, NeoplasticGenes, NeoplasmGliomaHumansMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesEnzyme InhibitorsMatrix Metalloproteinase InhibitorsMatrix MetalloproteinasesMicroRNAsMIRN21 microRNA, humanRNA, Messenger

Identifiers

PMID18591254
PMCPMC2519720
OpenAlexW2163655902

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.