Evidence map›Paper›PMID 30425720›Full record

ArticleFrontiers in immunology2018

Adenosinergic Signaling Alters Natural Killer Cell Functional Responses.

Andrea M Chambers, Jiao Wang, Kyle B Lupo, Hao Yu, Nadia M Atallah Lanman, Sandro Matosevic

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

75 citing papers in PubMed, 116 citations in OpenAlex.

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  10. Therapeutic potential of CD73Histology and histopathology · 2025
    Review
  11. Rendering NK Cells Antigen-Specific for the Therapy of Solid Tumours.International journal of molecular sciences · 2025
    Review
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15 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

6 authors at 2 institutions in 1 country.

Andrea M ChambersDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN, United States.
Jiao WangDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN, United States.
Kyle B LupoDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN, United States.
Hao YuCenter for Cancer Research, Purdue University, West Lafayette, IN, United States.
Nadia M Atallah LanmanCenter for Cancer Research, Purdue University, West Lafayette, IN, United States.
Sandro MatosevicDepartment of Industrial and Physical Pharmacy, Purdue University, West Lafayette, IN, United States.
Purdue University West Lafayette · USCenter for Cancer Research · US

Funding

Transgenic Mouse Core Facility Shared Resource (TMCF-SR)P30CA023168 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI John Tesmer · 1985 to 2026
$43.4M
Indiana Clinical and Translational Sciences InstituteUL1TR001108 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$23.3M
Indiana Clinical and Translational Sciences InstituteTL1TR001107 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI DENNE, SCOTT C., SHEKHAR, ANANTHA · 2013 to 2017
$2.0M
NCATS NIH HHS TL1 TR001107NCATS NIH HHS UL1 TR001108NCI NIH HHS P30 CA023168
6 · The paper itself

Abstract

Adenosine is a potent immunosuppressive purine metabolite contributing to the pathogenesis of solid tumors. Extracellular adenosine signals on tumor-infiltrating NK cells to inhibit their proliferation, maturation, and cytotoxic function. Cytokine priming imparts upon NK cells distinct activation statuses, which modulate NK anti-tumor immunity and responses to purinergic metabolism. Here, for the first time, we investigated human NK cell responses to adenosinergic signaling in the context of distinct cytokine priming programs. NK cells were shown to be hyper-responsive to adenosine when primed with IL-12 and IL-15 compared to IL-2, exhibiting enhanced IFN-γ expression from CD56

Indexed as

AdenosineCD56 AntigenCell DifferentiationCell ProliferationCells, CulturedCytokinesCytotoxicity, ImmunologicHumansImmunotherapy, AdoptiveKiller Cells, NaturalLymphocyte ActivationNeoplasmsNK Cell Lectin-Like Receptor Subfamily KSignal TransductionTOR Serine-Threonine KinasesAdenosineCD56 AntigenCytokinesKLRK1 protein, humanNK Cell Lectin-Like Receptor Subfamily KTOR Serine-Threonine KinasesadenosineimmunometabolismimmunotherapyNK cellspurinergic signaling

Identifiers

PMID30425720
PMCPMC6218627
OpenAlexW2899022735

What OpenQuestion holds

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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.