Evidence map›Paper›PMID 31455353›Full record

ArticleCell communication and signaling : CCS2019

Giuseppina D'Alessandro, Deborah Quaglio, Lucia Monaco, Clotilde Lauro, Francesca Ghirga, Cinzia Ingallina, Michela De Martino, Sergio Fucile, Alessandra Porzia, Maria Amalia Di Castro and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

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  13. Precision Oncology via NMR-Based Metabolomics: A Review on Breast Cancer.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

21 authors at 8 institutions in 1 country.

Giuseppina D'AlessandroDepartment of Physiology and Pharmacology, Sapienza University, Rome, Italy.
Deborah QuaglioDepartment of Chemistry and Technology of Drugs, "Department of Excellence 2018-2022", Sapienza University of Rome, P.le Aldo Moro 5, 00185, Rome, Italy. deborah.quaglio@uniroma1.it.ORCID 0000-0001-7762-8283
Lucia MonacoDepartment of Physiology and Pharmacology, Sapienza University, Rome, Italy.
Clotilde LauroDepartment of Physiology and Pharmacology, Sapienza University, Rome, Italy.
Francesca GhirgaCenter For Life Nano Science@Sapienza, Istituto Italiano di Tecnologia, Rome, Italy.
Cinzia IngallinaDepartment of Chemistry and Technology of Drugs, "Department of Excellence 2018-2022", Sapienza University of Rome, P.le Aldo Moro 5, 00185, Rome, Italy.
Michela De MartinoDepartment of Chemistry and Technology of Drugs, "Department of Excellence 2018-2022", Sapienza University of Rome, P.le Aldo Moro 5, 00185, Rome, Italy.
Sergio FucileDepartment of Physiology and Pharmacology, Sapienza University, Rome, Italy.
Alessandra PorziaDepartment of Molecular Medicine, Laboratory affiliated to Istituto Pasteur Italia Fondazione Cenci Bolognetti, Sapienza University of Rome, Rome, Italy.
Maria Amalia Di CastroDepartment of Physiology and Pharmacology, Sapienza University, Rome, Italy.
Federica BellatoDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.
Francesca MastrottoDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.
Mattia MoriDepartment of Biotechnology, Chemistry and Pharmacy, "Department of Excellence 2018-2022", University of Siena, via Aldo Moro 2, 53100, Siena, Italy.
Paola InfanteCenter For Life Nano Science@Sapienza, Istituto Italiano di Tecnologia, Rome, Italy.
Paola TuranoCERM and Department of Chemistry, University of Florence, Via Luigi Sacconi 6, 50019, Sesto Fiorentino, Florence, Italy.
Stefano SalmasoDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.
Paolo CalicetiDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.
Lucia Di MarcotullioDepartment of Molecular Medicine, Laboratory affiliated to Istituto Pasteur Italia Fondazione Cenci Bolognetti, Sapienza University of Rome, Rome, Italy.
Bruno BottaDepartment of Chemistry and Technology of Drugs, "Department of Excellence 2018-2022", Sapienza University of Rome, P.le Aldo Moro 5, 00185, Rome, Italy.
Veronica GhiniCIRMMP, Via Luigi Sacconi 6, 50019, Sesto Fiorentino, Florence, Italy.
Cristina LimatolaIRCCS Neuromed, Pozzilli, IS, Italy.
Sapienza University of Rome · ITUniversity of Padua · ITIstituto Neurologico Mediterraneo · ITIstituto Pasteur · ITItalian Institute of Technology · ITInteruniversity Consortium for Magnetic Resonance · ITUniversity of Florence · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGlioma is the most common and primary brain tumors in adults. Despite the available multimodal therapies, glioma patients appear to have a poor prognosis. The Hedgehog (Hh) signaling is involved in tumorigenesis and emerged as a promising target for brain tumors. Glabrescione B (GlaB) has been recently identified as the first direct inhibitor of Gli1, the downstream effector of the pathway.

methodsWe established the overexpression of Gli1 in murine glioma cells (GL261) and GlaB effect on cell viability. We used

resultsWe found that GlaB affected the growth of murine glioma cells both in vitro and in vivo animal model. Using an untargeted

conclusionsOur results indicate that GlaB inhibits glioma cell growth and exacerbates Warburg effect, increasing lactate production. In addition, the simultaneous blockade of Gli1 and lactate efflux amplifies the anti-tumor effect in vivo, providing new potential therapeutic strategy for this brain tumor.

Indexed as

MetabolomicsAnimalsCell ProliferationChromonesGliomaGlycolysisHumansMaleMiceNeoplasms, ExperimentalProton Magnetic Resonance SpectroscopySignal TransductionTumor Cells, CulturedChromonesglabrescione B1H-NMR spectroscopyGliomaHh pathwayIsoflavonesMetabolomics

Identifiers

PMID31455353
PMCPMC6712882
OpenAlexW2970633661

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.