Evidence map›Paper›PMID 19825957›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2009

Increased ectonucleotidase expression and activity in regulatory T cells of patients with head and neck cancer.

Magis Mandapathil, Miroslaw J Szczepanski, Marta Szajnik, Jin Ren, Diana E Lenzner, Edwin K Jackson, Elieser Gorelik, Stephan Lang, Jonas T Johnson, Theresa L Whiteside

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

107 citing papers in PubMed, 182 citations in OpenAlex.

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  18. An overview of current therapeutic strategies for glioblastoma and the role of CD73 as an alternative curative approach.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
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47 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

10 authors at 2 institutions in 2 countries.

Magis MandapathilUniversity of Pittsburgh Cancer Institute and Department of Pathology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Miroslaw J Szczepanski
Marta Szajnik
Jin Ren
Diana E Lenzner
Edwin K Jackson
Elieser Gorelik
Stephan Lang
Jonas T Johnson
Theresa L Whiteside
UPMC Hillman Cancer Center · USUniversity of Duisburg-Essen · DE

Funding

Tissue Procurement / ImmunohistologyP01CA109688 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BECICH, MICHAEL JOHN · 2006 to 2010
$5.9M
NCI NIH HHS P01 CA109688NHLBI NIH HHS N01 HB037165
6 · The paper itself

Abstract

purposeRegulatory T cell (Treg) frequency and activity are increased in cancer patients and play a major role in tumor escape. Although disease progression is favored by the presence of Treg, mechanisms used by Treg to suppress antitumor immunity are unknown. The ectonucleotidases CD39 and CD73 are expressed in Treg and convert ATP into immunosuppressive adenosine. In this study, the involvement of the adenosinergic pathway in Treg-mediated suppression in head and neck squamous cell carcinoma (HNSCC) patients was evaluated. EXPERIMENTAL

designHNSCC patients with an active disease (n = 19) and patients with no evident disease after therapy (n = 14) were studied. Ectonucleotidase expression on CD4(+) T cells and CD4(+)CD25(high) Treg was evaluated by flow cytometry and compared with normal controls. Ectonucleotidase activity was also compared within these three groups. The data were analyzed for associations of ectonucleotidase expression/function with disease stage.

resultsThe percentages and expression levels of CD39 and CD73 in CD4(+) T cells and Treg were greater in HNSCC than in normal controls and highest in patients with no evident disease. Patients' Treg hydrolyzed ATP at higher rates and produced higher levels of adenosine than normal controls' Treg. The increased frequency and enzymatic activity of CD4(+)CD39(+) cells corresponded to increased adenosine-mediated suppression of effector T cells, which was partly inhibited by ARL67156, an ectonucleotidase inhibitor, and by ZM241385, a selective A(2a)/A(2b) receptor antagonist.

conclusionsCD39(+) Treg frequency and adenosine-mediated suppression are significantly increased in HNSCC patients. The adenosinergic pathway is involved in Treg-mediated immunosuppression in cancer and its attenuation could be a promising immunotherapeutic strategy for patients with HNSCC.

Indexed as

5'-NucleotidaseAdenosine TriphosphateAdultAgedAntigens, CDApyraseCarcinoma, Squamous CellCD4-Positive T-LymphocytesFemaleHead and Neck NeoplasmsHumansImmunosuppression TherapyMaleMiddle AgedN-Glycosyl HydrolasesT-Lymphocytes, Regulatory5'-Nucleotidaseadenosine nucleosidaseAdenosine TriphosphateAntigens, CDApyraseCD39 antigenN-Glycosyl Hydrolases

Identifiers

PMID19825957
PMCPMC2763335
OpenAlexW2111585885

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Registered trials

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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.