Evidence map›Paper›PMID 30655604›Full record

ArticleOncogene2019

The P2X7 receptor modulates immune cells infiltration, ectonucleotidases expression and extracellular ATP levels in the tumor microenvironment.

Elena De Marchi, Elisa Orioli, Anna Pegoraro, Sabina Sangaletti, Paola Portararo, Antonio Curti, Mario Paolo Colombo, Francesco Di Virgilio, Elena Adinolfi

Open access · hybridAbstract read
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed, 1 pooled it
18.0field-weighted citation impact, top 1% 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

133 citing papers in PubMed, 1 synthesis or guideline pooled it, 188 citations in OpenAlex.

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  11. Targeting CD39 as a Therapeutic for Cancer Immunotherapy.Expert reviews in molecular medicine · 2026
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73 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Elena De MarchiDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, University of Ferrara, Via Luigi Borsari, 46, 44121, Ferrara, Italy.
Elisa OrioliDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, University of Ferrara, Via Luigi Borsari, 46, 44121, Ferrara, Italy.
Anna PegoraroDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, University of Ferrara, Via Luigi Borsari, 46, 44121, Ferrara, Italy.
Sabina SangalettiDepartment of Experimental Oncology, Molecular Immunology Unit, Istituto Nazionale dei Tumori (IRCCS), Via Amadeo, 42, 20133, Milan, Italy.
Paola PortararoDepartment of Experimental Oncology, Molecular Immunology Unit, Istituto Nazionale dei Tumori (IRCCS), Via Amadeo, 42, 20133, Milan, Italy.
Antonio CurtiDepartment of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology L. and A. Seràgnoli, S. Orsola-Malpighi Hospital, University of Bologna, via Massarenti, 9, 40138, Bologna, Italy.
Mario Paolo ColomboDepartment of Experimental Oncology, Molecular Immunology Unit, Istituto Nazionale dei Tumori (IRCCS), Via Amadeo, 42, 20133, Milan, Italy.
Francesco Di VirgilioDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, University of Ferrara, Via Luigi Borsari, 46, 44121, Ferrara, Italy.ORCID http://orcid.org/0000-0003-3566-1362
Elena AdinolfiDepartment of Morphology, Surgery and Experimental Medicine, Section of Pathology, Oncology and Experimental Biology, University of Ferrara, Via Luigi Borsari, 46, 44121, Ferrara, Italy. elena.adinolfi@unife.it.ORCID http://orcid.org/0000-0001-8129-9929
University of Ferrara · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the tumor microenvironment (TME) ATP and its receptor P2X7 exert a pivotal influence on cancer growth and tumor-host interactions. Here we analyzed the different effect of P2X7 genetic deficiency versus its antagonism on response against P2X7-expressing implanted tumors. We focused on immune cell expression of ATP degrading enzymes CD39 and CD73 and in vivo measured TME's ATP. The immune infiltrate of tumors growing in P2X7 null mice shows a decrease in CD8

Indexed as

5'-NucleotidaseAdenosine TriphosphateAnimalsAntigens, DifferentiationCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell Line, TumorLymphocytes, Tumor-InfiltratingMice, Inbred BALB CMice, Inbred C57BLMice, Mutant StrainsProgrammed Cell Death 1 ReceptorPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7T-Lymphocytes, RegulatoryTumor Microenvironment5'-NucleotidaseAdenosine TriphosphateAntigens, DifferentiationOX40IgP2rx7 protein, mousePdcd1 protein, mouseProgrammed Cell Death 1 ReceptorPurinergic P2X Receptor AntagonistsReceptors, Purinergic P2X7

Identifiers

PMID30655604
PMCPMC6756114
OpenAlexW2909260710

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.