Evidence map›Paper›PMID 37762206›Full record

ReviewInternational journal of molecular sciences2023

The P2X7 Receptor in Oncogenesis and Metastatic Dissemination: New Insights on Vesicular Release and Adenosinergic Crosstalk.

Elena Adinolfi, Elena De Marchi, Marianna Grignolo, Bartosz Szymczak, Anna Pegoraro

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

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  10. P2X7 Variants in Pathophysiology.International journal of molecular sciences · 2024
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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

5 authors at 2 institutions in 2 countries.

Elena AdinolfiSection of Experimental Medicine, Department of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Elena De MarchiSection of Experimental Medicine, Department of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.ORCID 0000-0003-0064-4335
Marianna GrignoloSection of Experimental Medicine, Department of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Bartosz SzymczakDepartment of Biochemistry, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Torun, 87-100 Torun, Poland.ORCID 0000-0001-7597-4238
Anna PegoraroSection of Experimental Medicine, Department of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
University of Ferrara · ITNicolaus Copernicus University · PL

Funding

European Cooperation in Science and Technology CA21130Italian Association for Cancer Research IG22837TRANSCAN-3 JTC2021 PUR-THER, TRANSCAN3_00094
6 · The paper itself

Abstract

The tumor niche is an environment rich in extracellular ATP (eATP) where purinergic receptors have essential roles in different cell subtypes, including cancer, immune, and stromal cells. Here, we give an overview of recent discoveries regarding the role of probably the best-characterized purinergic receptor in the tumor microenvironment: P2X7. We cover the activities of the P2X7 receptor and its human splice variants in solid and liquid cancer proliferation, dissemination, and crosstalk with immune and endothelial cells. Particular attention is paid to the P2X7-dependent release of microvesicles and exosomes, their content, including ATP and miRNAs, and, in general, P2X7-activated mechanisms favoring metastatic spread and niche conditioning. Moreover, the emerging role of P2X7 in influencing the adenosinergic axis, formed by the ectonucleotidases CD39 and CD73 and the adenosine receptor A2A in cancer, is analyzed. Finally, we cover how antitumor therapy responses can be influenced by or can change P2X7 expression and function. This converging evidence suggests that P2X7 is an attractive therapeutic target for oncological conditions.

Indexed as

AdenosineCarcinogenesisNeoplasmsReceptors, Purinergic P2X7Adenosine TriphosphateAnimalsApyraseExosomesHumansNeoplasm MetastasisTumor MicroenvironmentAdenosineAdenosine TriphosphateApyraseReceptors, Purinergic P2X7ATPcancerexosomesmetastasismicrovesiclesP2X7

Identifiers

PMID37762206
PMCPMC10531279
OpenAlexW4386602010

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.