Evidence map›Paper›PMID 21242969›Full record

ArticleOncogene2011

P2X(7) receptor activation enhances SK3 channels- and cystein cathepsin-dependent cancer cells invasiveness.

B Jelassi, A Chantôme, F Alcaraz-Pérez, A Baroja-Mazo, M L Cayuela, P Pelegrin, A Surprenant, S Roger

Abstract read
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In one paragraph

Article in Oncogene, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
11.4field-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

119 citing papers in PubMed, 206 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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  6. Review
  7. Article
  8. P2X7 Variants in Pathophysiology.International journal of molecular sciences · 2024
    Review
  9. Article
  10. Differential contribution of THIK-1 KJournal of neuroinflammation · 2024
    Article
  11. Article
  12. Review
  13. Review
  14. Animal Models for the Investigation of P2X7 Receptors.International journal of molecular sciences · 2023
    Review
  15. Research Progress in the Relationship Between P2X7R and Cervical Cancer.Reproductive sciences (Thousand Oaks, Calif.) · 2023
    Review
  16. Review
  17. Spotlight on P2X7 Receptor PET Imaging: A Bright Target or a Failing Star?International journal of molecular sciences · 2023
    Review
  18. Review
  19. Review
  20. Review

59 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

8 authors at 4 institutions in 3 countries.

B JelassiUniversité François Rabelais de Tours, France.
A Chantôme
F Alcaraz-Pérez
A Baroja-Mazo
M L Cayuela
P Pelegrin
A Surprenant
S Roger
Hospital Universitario Virgen de la Arrixaca · ESInserm · FRUniversity of Manchester · GBUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ATP-gated P2X(7) receptors (P2X(7)R) are unusual plasma membrane ion channels that have been extensively studied in immune cells. More recently, P2X(7)R have been described as potential cancer cell biomarkers. However, mechanistic links between P2X(7)R and cancer cell processes are unknown. Here, we show, in the highly aggressive human breast cancer cell line MDA-MB-435s, that P2X(7) receptor is highly expressed and fully functional. Its activation is responsible for the extension of neurite-like cellular prolongations, of the increase in cell migration by 35% and in cell invasion through extracellular matrix by 150%. The change in cancer cell morphology and the increased migration appeared to be due to the activation of Ca(2+)-activated SK3 potassium channels. The enhanced invasion through the extracellular matrix was related to the increase of mature forms of cysteine cathepsins in the extracellular medium, which was independent of SK3 channel activity and not associated with cell death. Pharmacological targeting of P2X(7)R in vivo was crucial for cell invasiveness in a zebrafish model of metastases. Our results demonstrate a novel mechanistic link between P2X(7)R functionality in cancer cells and invasiveness, a key parameter in tumour growth and in the development of metastases. They also suggest a potential therapeutic role for the newly developed P2X(7)R antagonists.

Indexed as

Neoplasm InvasivenessCathepsinsCell Line, TumorHumansPurinergic AgonistsReceptors, Purinergic P2X7Small-Conductance Calcium-Activated Potassium ChannelsCathepsinsKCNN3 protein, humanPurinergic AgonistsReceptors, Purinergic P2X7Small-Conductance Calcium-Activated Potassium Channels

Identifiers

PMID21242969
OpenAlexW2000988880

What OpenQuestion holds

Textmetadata
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.