Evidence map›Paper›PMID 34768902›Full record

ArticleInternational journal of molecular sciences2021

Expression Pattern of Purinergic Signaling Components in Colorectal Cancer Cells and Differential Cellular Outcomes Induced by Extracellular ATP and Adenosine.

Clémentine Dillard, Chloé Borde, Ammara Mohammad, Virginie Puchois, Laurent Jourdren, Annette K Larsen, Michèle Sabbah, Vincent Maréchal, Alexandre E Escargueil, Elodie Pramil

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. P2YJournal of immunology research · 2026
    Article
  6. Review
  7. World journal of clinical oncology · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Amplified CaInternational journal of cancer · 2022
    Article
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

10 authors at 2 institutions in 1 country.

Clémentine DillardCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.
Chloé BordeCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.
Ammara MohammadGenomics Core Facility, Institut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France.
Virginie PuchoisCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.
Laurent JourdrenGenomics Core Facility, Institut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, Université PSL, CNRS, INSERM, F-75005 Paris, France.ORCID 0000-0003-4253-1048
Annette K LarsenCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.
Michèle SabbahCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.ORCID 0000-0001-5368-9022
Vincent MaréchalCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.
Alexandre E EscargueilCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.ORCID 0000-0002-7419-7518
Elodie PramilCentre de Recherche Saint-Antoine, Sorbonne Université, INSERM U938, F-75012 Paris, France.
Inserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purine nucleotide adenosine triphosphate (ATP) is known for its fundamental role in cellular bioenergetics. However, in the last decades, different works have described emerging functions for ATP, such as that of a danger signaling molecule acting in the extracellular space on both tumor and stromal compartments. Beside its role in immune cell signaling, several studies have shown that high concentrations of extracellular ATP can directly or indirectly act on cancer cells. Accordingly, it has been reported that purinergic receptors are widely expressed in tumor cells. However, their expression pattern is often associated with contradictory cellular outcomes. In this work, we first investigated gene expression profiles through "RNA-Sequencing" (RNA Seq) technology in four colorectal cancer (CRC) cell lines (HT29, LS513, LS174T, HCT116). Our results demonstrate that CRC cells mostly express the A2B, P2X4, P2Y1, P2Y2 and P2Y11 purinergic receptors. Among these, the P2Y1 and P2Y2 coding genes are markedly overexpressed in all CRC cells compared to the HCEC-1CT normal-like colonic cells. We then explored the cellular outcomes induced by extracellular ATP and adenosine. Our results show that in terms of cell death induction extracellular ATP is consistently more active than adenosine against CRC, while neither compound affected normal-like colonic cell survival. Intriguingly, while for the P2Y2 receptor pharmacological inhibition completely abolished the rise in cytoplasmic Ca

Indexed as

AdenosineAdenosine TriphosphateApoptosisBiomarkers, TumorCalciumCalcium SignalingCell CycleCell ProliferationColorectal NeoplasmsExtracellular SpaceGene Expression Regulation, NeoplasticHumansReceptors, PurinergicTranscriptomeTumor Cells, CulturedAdenosineAdenosine TriphosphateBiomarkers, TumorCalciumReceptors, Purinergic2D/3D cell cultureCa2+ mobilizationcell cycle arrestcell death inductioncyclic nucleotides modulationextracellular ATPpurinergic receptors

Identifiers

PMID34768902
PMCPMC8583864
OpenAlexW3211013249

What OpenQuestion holds

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LicenceCC BY
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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.