Evidence map›Paper›PMID 28978137›Full record

ArticleOncotarget2017

The histone methyltransferase EZH2 as a druggable target in SHH medulloblastoma cancer stem cells.

Evelina Miele, Sergio Valente, Vincenzo Alfano, Marianna Silvano, Paolo Mellini, Diana Borovika, Biagina Marrocco, Agnese Po, Zein Mersini Besharat, Giuseppina Catanzaro and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 51 citations in OpenAlex.

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  13. EHMT2/G9a as an Epigenetic Target in Pediatric and Adult Brain Tumors.International journal of molecular sciences · 2021
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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

20 authors at 5 institutions in 2 countries.

Evelina Miele *Center for Life NanoScience@Sapienza, Istituto Italiano di Tecnologia, Rome 00161, Italy.
Sergio Valente *Department of Chemistry and Technologies of Drugs, Sapienza University of Rome, Rome 00185, Italy.
Vincenzo AlfanoDepartment of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Marianna SilvanoDepartment of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Paolo MelliniDepartment of Chemistry and Technologies of Drugs, Sapienza University of Rome, Rome 00185, Italy.
Diana BorovikaLatvian Institute of Organic Synthesis, Riga LV-1006, Latvia.
Biagina MarroccoDepartment of Chemistry and Technologies of Drugs, Sapienza University of Rome, Rome 00185, Italy.
Agnese PoDepartment of Molecular Medicine, Sapienza University of Rome, Rome 00161, Italy.
Zein Mersini BesharatDepartment of Molecular Medicine, Sapienza University of Rome, Rome 00161, Italy.
Giuseppina CatanzaroDepartment of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Giuseppe BattagliaNeuromed Institute, Località Camerelle, Pozzilli 86077, Italy.
Luana AbballeDepartment of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Clemens ZwergelDepartment of Chemistry and Technologies of Drugs, Sapienza University of Rome, Rome 00185, Italy.
Giulia StaziDepartment of Chemistry and Technologies of Drugs, Sapienza University of Rome, Rome 00185, Italy.
Ciro MiliteDepartment of Pharmacy, University of Salerno, Fisciano 84084, Italy.
Sabrina CastellanoDepartment of Pharmacy, University of Salerno, Fisciano 84084, Italy.
Marco TafaniDepartment of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Peteris TrapencierisLatvian Institute of Organic Synthesis, Riga LV-1006, Latvia.
Antonello MaiDepartment of Chemistry and Technologies of Drugs, Sapienza University of Rome, Rome 00185, Italy.
Elisabetta FerrettiDepartment of Experimental Medicine, Sapienza University of Rome, Rome 00161, Italy.
Sapienza University of Rome · ITIstituto Neurologico Mediterraneo · ITLatvijas Organiskās Sintēzes Institūts · LVUniversity of Salerno · ITIstituti di Ricovero e Cura a Carattere Scientifico · IT

Funding

Histone Lysine deMethylation: Structures, Inhibitions and MechanismsR01GM114306 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CHENG, XIAODONG · 2015 to 2018
$1.2M
NIGMS NIH HHS R01 GM114306
6 · The paper itself

Abstract

The histone methyltransferase EZH2 plays a role in maintenance of the stem component of cancer, and its overexpression and/or mutation typically drives tumor aggressiveness, drug resistance and patients' poor prognosis. In this study, we use mouse and human medulloblastoma stem-like cells belonging to the Sonic Hedgehog subgroup (SHH MB-SLCs) and demonstrate that genetic suppression of EZH2 reduces the level of its histone mark H3K27me3 and lowers proliferation and self-renewal. We designed an EZH2 inhibitor (EZH2i) as a simplified analog of EPZ005687 and GSK2816126, MC3629, and we tested its biological activity in SHH MB-SLCs. Pharmacological inhibition of EZH2 impairs SHH MB cells proliferation and self-renewal, and induces apoptosis

Indexed as

EZH2 inhibitorshedgehog pathwayhistone methyltransferasemedulloblastoma stem-like cellsself-renewal

Identifiers

PMID28978137
PMCPMC5620277
OpenAlexW2741344135

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.