Evidence map›Paper›PMID 24156018›Full record

ArticleCancer medicine2013

Inhibition of MMP14 potentiates the therapeutic effect of temozolomide and radiation in gliomas.

Ilya Ulasov, Bart Thaci, Purvaba Sarvaiya, Ruiyang Yi, Donna Guo, Brenda Auffinger, Peter Pytel, Lingjiao Zhang, Chung Kwon Kim, Anton Borovjagin and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. MMP14-Dependent Activation of TGF-β Signaling Enhances Malignancies via Promoting Necroptosis in Glioblastoma.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  18. Plasma Proteins As Biodosimetric Markers of Low-Dose Radiation in Mice.Dose-response : a publication of International Hormesis Society
    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

14 authors at 4 institutions in 2 countries.

Ilya UlasovThe Brain Tumor Center, The University of Chicago Chicago, Illinois, 60637.
Bart Thaci
Purvaba Sarvaiya
Ruiyang Yi
Donna Guo
Brenda Auffinger
Peter Pytel
Lingjiao Zhang
Chung Kwon Kim
Anton Borovjagin
Mahua Dey
Yu Han
Anatoly Y Baryshnikov
Maciej S Lesniak
University of Chicago · USCentral Brain Tumor Registry of the United States · USRussian Cancer Research Center NN Blokhin · RUUniversity of Alabama · US

Funding

Regulatory T Cells and Oncolytic Virotherapy of GliomaR01CA122930 · NCI · UNIVERSITY OF CHICAGO · PI LESNIAK, MACIEJ S · 2008 to 2015
$2.5M
NCI NIH HHS R01 CA122930NCI NIH HHS R01-CA122930
6 · The paper itself

Abstract

Metalloproteinases are membrane-bound proteins that play a role in the cellular responses to antiglioma therapy. Previously, it has been shown that treatment of glioma cells with temozolomide (TMZ) and radiation (XRT) induces the expression of metalloproteinase 14 (MMP14). To investigate the role of MMP14 in gliomagenesis, we used several chemical inhibitors which affect MMP14 expression. Of all the inhibitors tested, we found that Marimastat not only inhibits the expression of MMP14 in U87 and U251 glioma cells, but also induces cell cycle arrest. To determine the relationship between MMP14 inhibition and alteration of the cell cycle, we used an RNAi technique. Genetic knockdown of MMP14 in U87 and U251 glioma cells induced G2/M arrest and decreased proliferation. Mechanistically, we show that TMZ and XRT regulated expression of MMP14 in clinical samples and in vitro models through downregulation of microRNA374. In vivo genetic knockdown of MMP14 significantly decreased tumor growth of glioma xenografts and improved survival of glioma-bearing mice. Moreover, the combination of MMP14 silencing with TMZ and XRT significantly improved the survival of glioma-bearing mice compared to a single modality treatment group. Therefore, we show that the inhibition of MMP14 sensitizes tumor cells to TMZ and XRT and could be used as a future strategy for antiglioma therapy.

Indexed as

RadiationAnimalsAntineoplastic Agents, AlkylatingBrain NeoplasmsCell DivisionCell Line, TumorCell ProliferationCell SurvivalDacarbazineDisease Models, AnimalFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGene SilencingGliomaHumansAntineoplastic Agents, AlkylatingDacarbazineMatrix Metalloproteinase 14MicroRNAsMIRN374 microRNA 374, humanTemozolomideBrain cancergliomaMMP14radiationtemozolomide

Identifiers

PMID24156018
PMCPMC3799280
OpenAlexW2040830156

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.