Evidence map›Paper›PMID 28174424›Full record

ReviewImmunology and cell biology2017

Targeting A2 adenosine receptors in cancer.

David Allard, Martin Turcotte, John Stagg

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Immunology and cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
10.7field-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

62 citing papers in PubMed, 106 citations in OpenAlex.

  1. The Randomized Phase II ARC-9 Study of Etrumadenant-Based Therapy versus Regorafenib in Patients with Previously Treated Metastatic Colorectal Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Trial
  2. Clinical significance of CD73 in triple-negative breast cancer: multiplex analysis of a phase III clinical trial.Annals of oncology : official journal of the European Society for Medical Oncology · 2018
    Trial
  3. Exercise as a modulator of purinergic signaling and inflammation in cancer-associated sarcopenia: a narrative review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  4. Review
  5. Article
  6. Adenosine APharmaceuticals (Basel, Switzerland) · 2026
    Article
  7. Review
  8. Review
  9. Review
  10. Insights from Clinical Trials on AACS pharmacology & translational science · 2025
    Review
  11. APurinergic signalling · 2025
    Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Pioneering biomimetic biomaterial for leukemia therapy enhancement: a review.Frontiers in bioengineering and biotechnology · 2025
    Review
  17. Review
  18. Review
  19. Review
  20. AInternational journal of molecular sciences · 2023
    Article

2 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

3 authors at 2 institutions in 1 country.

David AllardCentre de Recherche du, Centre Hospitalier de l'Université de Montréal, et Institut du Cancer de Montréal, Montréal, Québec, Canada.
Martin TurcotteCentre de Recherche du, Centre Hospitalier de l'Université de Montréal, et Institut du Cancer de Montréal, Montréal, Québec, Canada.
John StaggCentre de Recherche du, Centre Hospitalier de l'Université de Montréal, et Institut du Cancer de Montréal, Montréal, Québec, Canada.
Université de Montréal · CACentre Hospitalier de l’Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor cells use various ways to evade anti-tumor immune responses. Adenosine, a potent immunosuppressive metabolite, is often found elevated in the extracellular tumor microenvironment. Therefore, targeting adenosine-generating enzymes (CD39 and CD73) or adenosine receptors has emerged as a novel means to stimulate anti-tumor immunity. In particular, the A2 (A2a and A2b) adenosine receptors exhibit similar immunosuppressive and pro-angiogenic functions, yet have distinct biological roles in cancer. In this review, we describe the common and distinct biological consequences of A2a and A2b adenosine receptor signaling in cancer. We discuss recent pre-clinical studies and summarize the different mechanisms-of-action of adenosine-targeting drugs. We also review the rationale for combining inhibitors of the adenosine pathway with other anticancer therapies such immune checkpoint inhibitors, tumor vaccines, chemotherapy and adoptive T cell therapy.

Indexed as

5'-NucleotidaseAdenosine A2 Receptor AntagonistsAnimalsAntibodies, MonoclonalAntigens, CDAntineoplastic AgentsApyraseCancer VaccinesCombined Modality TherapyCostimulatory and Inhibitory T-Cell ReceptorsHumansImmunityImmunotherapy, AdoptiveMolecular Targeted TherapyNeoplasmsNeovascularization, Pathologic5'-NucleotidaseAdenosine A2 Receptor AntagonistsAntibodies, MonoclonalAntigens, CDAntineoplastic AgentsApyraseCancer VaccinesCD39 antigenCostimulatory and Inhibitory T-Cell ReceptorsReceptors, Adenosine A2

Identifiers

PMID28174424
OpenAlexW2586318013

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.