Evidence map›Paper›PMID 36212741›Full record

ArticleNeuro-oncology advances

Targeting extracellular matrix remodeling sensitizes glioblastoma to ionizing radiation.

Varsha Thakur, Vijay S Thakur, Brittany Aguila, Tatiana I Slepak, Man Wang, Wei Song, Mohini Konai, Shahriar Mobashery, Mayland Chang, Ayush B Rana and 6 more

Open access · goldAbstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 6 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

16 authors at 2 institutions in 1 country.

Varsha ThakurPhillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.
Vijay S ThakurSylvester Comprehensive Cancer Center, Miami, Florida, USA.
Brittany AguilaSylvester Comprehensive Cancer Center, Miami, Florida, USA.
Tatiana I SlepakDepartment of Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.
Man WangDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
Wei SongDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
Mohini KonaiDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
Shahriar MobasheryDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
Mayland ChangDepartment of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana, USA.
Ayush B RanaSylvester Comprehensive Cancer Center, Miami, Florida, USA.
Dazhi WangSylvester Comprehensive Cancer Center, Miami, Florida, USA.
Juliano Tiburcio de FreitasPhillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.
Sakir Humayun GultekinNeuropathology, Division of Anatomic Pathology, University of Miami Miller School of Medicine, Miami, Florida, USA.
Scott M WelfordSylvester Comprehensive Cancer Center, Miami, Florida, USA.
Michael E IvanDepartment of Neurological Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID https://orcid.org/0000-0002-4798-4989
Barbara BedogniPhillip Frost Department of Dermatology and Cutaneous Surgery, University of Miami Miller School of Medicine, Miami, Florida, USA.ORCID https://orcid.org/0000-0002-1539-9064
University of Miami · USUniversity of Notre Dame · US

Funding

Polyamine Catabolism and Therapeutic Resistance in Glioblastoma MultiformeR01CA187053 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WELFORD, SCOTT MICHAEL · 2015 to 2025
$3.5M
NCI NIH HHS R01 CA187053
6 · The paper itself

Abstract

Background: The median survival of Glioblastoma multiforme (GBM) patients is 14+ months due to poor responses to surgery and chemoradiation. Means to counteract radiation resistance are therefore highly desirable. We demonstrate the membrane bound matrix metalloproteinase MT1-MMP promotes resistance of GBM to radiation, and that using a selective and brain permeable MT1-MMP inhibitor, Methods: Public microarray and RNA-sequencing data were used to determine MT1-MMP relevance in GBM patient survival. Glioma stem-like neurospheres (GSCs) were used for both in vitro and in vivo assays. An affinity resin coupled with proteomics was used to quantify active MT1-MMP in brain tissue of GBM patients. Short hairpin RNA (shRNA)-mediated knockdown of MT1-MMP and inhibition via the MT1-MMP inhibitor Results: MT1-MMP expression inversely correlated with patient survival. Active MT1-MMP was present in brain tissue of GBM patients but not in normal brain. shRNA- or Conclusions: MT1-MMP is pivotal in maintaining replication fork stability. Disruption of MT1-MMP sensitizes cells to radiation and can counteract invasion.

Indexed as

GBMMT1-MMPradiation resistanceradio-sensitization(R)-ND336

Identifiers

PMID36212741
PMCPMC9536293
OpenAlexW4295874972

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.