Evidence map›Paper›PMID 32098295›Full record

ArticleInternational journal of molecular sciences2020

Peptidylarginine Deiminase Isozyme-Specific PAD2, PAD3 and PAD4 Inhibitors Differentially Modulate Extracellular Vesicle Signatures and Cell Invasion in Two Glioblastoma Multiforme Cell Lines.

Pinar Uysal-Onganer, Amy MacLatchy, Rayan Mahmoud, Igor Kraev, Paul R Thompson, Jameel M Inal, Sigrun Lange

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
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  5. Citrullination in tumor immunity and therapy.The Journal of clinical investigation · 2025
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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

7 authors at 4 institutions in 2 countries.

Pinar Uysal-OnganerCancer Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK.ORCID 0000-0003-3190-8831
Amy MacLatchySchool of Life Sciences, University of Westminster, London W1W 6UW, UK.
Rayan MahmoudSchool of Life Sciences, University of Westminster, London W1W 6UW, UK.
Igor KraevElectron Microscopy Suite, Faculty of Science, Technology, Engineering and Mathematics, Open University, Milton Keynes MK7 6AA, UK.ORCID 0000-0003-1822-278X
Paul R ThompsonDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Jameel M InalSchool of Life and Medical Sciences, University of Hertfordshire, Hatfield AL10 9AB, UK.
Sigrun LangeTissue Architecture and Regeneration Research Group, School of Life Sciences, University of Westminster, London W1W 6UW, UK.ORCID 0000-0002-7193-3102
University of Westminster · GBLondon Metropolitan University · GBThe Open University · GBUniversity of Massachusetts Chan Medical School · US

Funding

Chemical probes to decipher PAD biologyR35GM118112 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Paul R Thompson · 2016 to 2026
$9.5M
NIGMS NIH HHS R35 GM118112
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM) is an aggressive adult brain tumour with poor prognosis. Roles for peptidylarginine deiminases (PADs) in GBM have recently been highlighted. Here, two GBM cell lines were treated with PAD2, PAD3 and PAD4 isozyme-specific inhibitors. Effects were assessed on extracellular vesicle (EV) signatures, including EV-microRNA cargo (miR21, miR126 and miR210), and on changes in cellular protein expression relevant for mitochondrial housekeeping (prohibitin (PHB)) and cancer progression (stromal interaction molecule 1 (STIM-1) and moesin), as well as assessing cell invasion. Overall, GBM cell-line specific differences for the three PAD isozyme-specific inhibitors were observed on modulation of EV-signatures, PHB, STIM-1 and moesin protein levels, as well as on cell invasion. The PAD3 inhibitor was most effective in modulating EVs to anti-oncogenic signatures (reduced miR21 and miR210, and elevated miR126), to reduce cell invasion and to modulate protein expression of pro-GBM proteins in LN229 cells, while the PAD2 and PAD4 inhibitors were more effective in LN18 cells. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways for deiminated proteins relating to cancer, metabolism and inflammation differed between the two GBM cell lines. Our findings highlight roles for the different PAD isozymes in the heterogeneity of GBM tumours and the potential for tailored PAD-isozyme specific treatment.

Indexed as

Cell Line, TumorCell MovementEnzyme InhibitorsExtracellular VesiclesGene Expression Regulation, NeoplasticHumansMicrofilament ProteinsMicroRNAsNeoplasm InvasivenessNeoplasm ProteinsProhibitinsProtein-Arginine Deiminase Type 2Protein-Arginine Deiminase Type 3Protein-Arginine Deiminase Type 4Repressor ProteinsStromal Interaction Molecule 1Enzyme InhibitorsMicrofilament ProteinsMicroRNAsmoesinNeoplasm ProteinsPHB protein, humanProhibitinsProtein-Arginine Deiminase Type 2Protein-Arginine Deiminase Type 3Protein-Arginine Deiminase Type 4Repressor ProteinsSTIM1 protein, humanStromal Interaction Molecule 1extracellular vesicles (EVs)glioblastoma multiforme (GBM)HIF-1microRNA (miR21, miR126, miR210)moesinpeptidylarginine deiminases (PADs)prohibitin (PHB)protein deiminationStromal interaction molecule 1 (STIM-1)

Identifiers

PMID32098295
PMCPMC7073130
OpenAlexW3008697461

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.