Evidence map›Paper›PMID 24681961›Full record

ArticleBlood cancer journal2014

5-Azacytidine treatment sensitizes tumor cells to T-cell mediated cytotoxicity and modulates NK cells in patients with myeloid malignancies.

A O Gang, T M Frøsig, M K Brimnes, R Lyngaa, M B Treppendahl, K Grønbæk, I H Dufva, P Thor Straten, S R Hadrup

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

52 citing papers in PubMed, 82 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

A O GangDepartment of Hematology, Center for Cancer Immune Therapy, University Hospital Herlev, Herlev, Denmark.
T M Frøsig1] Department of Hematology, Center for Cancer Immune Therapy, University Hospital Herlev, Herlev, Denmark [2] Department of Drug Design and Pharmacology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
M K BrimnesDepartment of Hematology, Center for Cancer Immune Therapy, University Hospital Herlev, Herlev, Denmark.
R LyngaaDepartment of Hematology, Center for Cancer Immune Therapy, University Hospital Herlev, Herlev, Denmark.
M B TreppendahlDepartment of Hematology, Rigshospitalet, Copenhagen, Denmark.
K GrønbækDepartment of Hematology, Rigshospitalet, Copenhagen, Denmark.
I H DufvaDepartment of Hematology, University Hospital Herlev, Herlev, Denmark.
P Thor StratenDepartment of Hematology, Center for Cancer Immune Therapy, University Hospital Herlev, Herlev, Denmark.
S R HadrupDepartment of Hematology, Center for Cancer Immune Therapy, University Hospital Herlev, Herlev, Denmark.
Herlev Hospital · DKRigshospitalet · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment with the demethylating agent 5-Azacytidine leads to prolonged survival for patients with myelodysplastic syndrome, and the demethylation induces upregulation of cancer-testis antigens. Cancer-testis antigens are well-known targets for immune recognition in cancer, and the immune system may have a role in this treatment regimen. We show here that 5-Azacytidine treatment leads to increased T-cell recognition of tumor cells. T-cell responses against a large panel of cancer-testis antigens were detected before treatment, and these responses were further induced upon initiation of treatment. These characteristics point to an ideal combination of 5-Azacytidine and immune therapy to preferentially boost T-cell responses against cancer-testis antigens. To initiate such combination therapy, essential knowledge is required about the general immune modulatory effect of 5-Azacytidine. We therefore examined potential treatment effects on both immune stimulatory (CD8 and CD4 T cells and Natural Killer (NK) cells) and immune inhibitory cell subsets (myeloid-derived suppressor cells and regulatory T cells). We observed a minor decrease and modulation of NK cells, but for all other populations no effects could be detected. Together, these data support a strategy for combining 5-Azacytidine treatment with immune therapy for potential clinical benefit.

Identifiers

PMID24681961
PMCPMC3972700
OpenAlexW1979859887

What OpenQuestion holds

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LicenceCC BY
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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.