Evidence map›Paper›PMID 34359950›Full record

ReviewCells2021

Cancer Metabostemness and Metabolic Reprogramming via P2X7 Receptor.

Izadora Lorrany Alves Rabelo, Vanessa Fernandes Arnaud-Sampaio, Elena Adinolfi, Henning Ulrich, Claudiana Lameu

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Purinergic system in cancer stem cells.Purinergic signalling · 2025
    Review
  4. Article
  5. Article
  6. P2X7 Variants in Pathophysiology.International journal of molecular sciences · 2024
    Review
  7. Review
  8. The P2 purinoceptors in prostate cancer.Purinergic signalling · 2023
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Emerging roles of purinergic signaling in anti-cancer therapy resistance.Frontiers in cell and developmental biology · 2022
    Review
  14. Review
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.

Izadora Lorrany Alves RabeloDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo 05508-000, Brazil.
Vanessa Fernandes Arnaud-SampaioDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo 05508-000, Brazil.
Elena AdinolfiDepartment of Medical Sciences, Section of Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy.
Henning UlrichDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo 05508-000, Brazil.ORCID 0000-0002-2114-3815
Claudiana LameuDepartamento de Bioquímica, Instituto de Química, Universidade de São Paulo, São Paulo 05508-000, Brazil.ORCID 0000-0002-6874-5864
Universidade de São Paulo · BRUniversity of Ferrara · IT

Funding

Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/19128-2Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/07366-4
6 · The paper itself

Abstract

The heterogeneity of tumor cell mass and the plasticity of cancer cell phenotypes in solid tumors allow for the insurgence of resistant and metastatic cells, responsible for cancer patients' clinical management's main challenges. Among several factors that are responsible for increased cancer aggression, metabolic reprogramming is recently emerging as an ultimate cancer hallmark, as it is central for cancer cell survival and self-renewal, metastasis and chemoresistance. The P2X7 receptor, whose expression is upregulated in many solid and hematological malignancies, is also emerging as a good candidate in cancer metabolic reprogramming and the regulation of stem cell proliferation and differentiation. Metabostemness refers to the metabolic reprogramming of cancer cells toward less differentiated (CSCs) cellular states, and we believe that there is a strong correlation between metabostemness and P2X7 receptor functions in oncogenic processes. Here, we summarize important aspects of P2X7 receptor functions in normal and tumor tissues as well as essential aspects of its structure, regulation, pharmacology and its clinical use. Finally, we review current knowledge implicating P2X7 receptor functions in cancer-related molecular pathways, in metabolic reprogramming and in metabostemness.

Indexed as

CarcinogenesisCell DifferentiationHumansNeoplasmsNeoplastic Stem CellsOncogenesReceptors, Purinergic P2X7Receptors, Purinergic P2X7cancer stem cellschemotherapy and chemoresistancemetabolic reprogrammingmetabolismmetastasisP2X7AP2X7BP2X7 receptorpurinergic signalingstemness

Identifiers

PMID34359950
PMCPMC8305434
OpenAlexW3181603106

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.