Evidence map›Paper›PMID 27980223›Full record

ArticleOncotarget2017

Extracellular ATP induces apoptosis through P2X7R activation in acute myeloid leukemia cells but not in normal hematopoietic stem cells.

Valentina Salvestrini, Stefania Orecchioni, Giovanna Talarico, Francesca Reggiani, Cristina Mazzetti, Francesco Bertolini, Elisa Orioli, Elena Adinolfi, Francesco Di Virgilio, Annalisa Pezzi and 3 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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  8. Purinergic system in cancer stem cells.Purinergic signalling · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. Animal Models for the Investigation of P2X7 Receptors.International journal of molecular sciences · 2023
    Review
  13. Review
  14. Article
  15. Article
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  17. Review
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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

13 authors at 4 institutions in 1 country.

Valentina SalvestriniDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Stefania OrecchioniEuropean Institute of Oncology, Milan, Italy.
Giovanna TalaricoEuropean Institute of Oncology, Milan, Italy.
Francesca ReggianiEuropean Institute of Oncology, Milan, Italy.
Cristina MazzettiDepartment Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Francesco BertoliniEuropean Institute of Oncology, Milan, Italy.
Elisa OrioliDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Elena AdinolfiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Francesco Di VirgilioDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
Annalisa PezziDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Michele CavoDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
Roberto M LemoliClinic of Hematology, Department of Internal Medicine (DiMI), University of Genoa, Genoa, Italy.
Antonio CurtiDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.
University of Bologna · ITEuropean Institute of Oncology · ITUniversity of Ferrara · ITUniversity of Genoa · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have shown that high ATP levels exhibit direct cytotoxic effects on several cancer cells types. Among the receptors engaged by ATP, P2X7R is the most consistently expressed by tumors. P2X7R is an ATP-gated ion channel that could drive the opening of a non-selective pore, triggering cell-death signal. We previously demonstrated that acute myeloid leukemia (AML) cells express high level of P2X7R. Here, we show that P2X7R activation with high dose ATP induces AML blast cells apoptosis. Moreover, P2X7R is also expressed on leukemic stem/progenitor cells (LSCs) which are sensitive to ATP-mediated cytotoxicity. Conversely, this cytotoxic effect was not observed on normal hematopoietic stem/progenitor cells (HSCs). Notably, the antileukemic activity of ATP was also observed in presence of bone marrow stromal cells and its addition to the culture medium enhanced cytosine arabinoside cytotoxicity despite stroma-induced chemoresistance. Xenotransplant experiments confirmed ATP antineoplastic activity in vivo.Overall, our results demonstrate that P2X7R stimulation by ATP induced a therapeutic response in AML at the LSC level while the normal stem cell compartment was not affected. These results provide evidence that ATP would be promising for developing innovative therapy for AML.

Indexed as

Transcriptional ActivationAdenosine TriphosphateAnimalsAntineoplastic AgentsApoptosisCell Line, TumorGene Expression Regulation, LeukemicHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteMiceReceptors, Purinergic P2X7Up-RegulationXenograft Model Antitumor AssaysAdenosine TriphosphateAntineoplastic AgentsP2RX7 protein, humanReceptors, Purinergic P2X7acute myeloid leukemia (AML)apoptosisATPleukemic stem cell (LSC)P2X7R

Identifiers

PMID27980223
PMCPMC5351599
OpenAlexW2566472201

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.