Evidence map›Paper›PMID 33042133›Full record

ArticleFrontiers in immunology2020

STAT1 Isoforms Differentially Regulate NK Cell Maturation and Anti-tumor Activity.

Katrin Meissl, Natalija Simonović, Lena Amenitsch, Agnieszka Witalisz-Siepracka, Klara Klein, Caroline Lassnig, Ana Puga, Claus Vogl, Andrea Poelzl, Markus Bosmann and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

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  7. Low-dose SAHA enhances CD8Cellular oncology (Dordrecht, Netherlands) · 2025
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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

14 authors at 3 institutions in 3 countries.

Katrin MeisslInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Natalija SimonovićInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Lena AmenitschInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Agnieszka Witalisz-SieprackaInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Klara KleinInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Caroline LassnigInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Ana PugaInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Claus VoglInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Andrea PoelzlInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Markus BosmannPulmonary Center, Department of Medicine, Boston University School of Medicine, Boston, MA, United States.
Alexander DohnalTumor Immunology, St. Anna Kinderkrebsforschung, Children's Cancer Research Institute, Vienna, Austria.
Veronika SexlInstitute of Pharmacology and Toxicology, University of Veterinary Medicine Vienna, Vienna, Austria.
Mathias MüllerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Birgit StroblInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
University of Veterinary Medicine Vienna · ATSt Anna Children's Hospital · ATUniversity Medical Center of the Johannes Gutenberg University Mainz · DE

Funding

Role reversal of MAVS in bacterial sepsisR01HL141513 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOSMANN, MARKUS · 2018 to 2022
$2.4M
New genetic models for C5a receptorsR01HL139641 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BOSMANN, MARKUS · 2018 to 2022
$2.1M
Austrian Science Fund FWF DOC 32NHLBI NIH HHS R01 HL139641NHLBI NIH HHS R01 HL141513
6 · The paper itself

Abstract

Natural killer (NK) cells are important components of the innate immune defense against infections and cancers. Signal transducer and activator of transcription 1 (STAT1) is a transcription factor that is essential for NK cell maturation and NK cell-dependent tumor surveillance. Two alternatively spliced isoforms of STAT1 exist: a full-length STAT1α and a C-terminally truncated STAT1β isoform. Aberrant splicing is frequently observed in cancer cells and several anti-cancer drugs interfere with the cellular splicing machinery. To investigate whether NK cell-mediated tumor surveillance is affected by a switch in STAT1 splicing, we made use of knock-in mice expressing either only the STAT1α (

Indexed as

AnimalsBone Marrow TransplantationCell Line, TumorCytotoxicity, ImmunologicImmunologic SurveillanceInterferon gamma ReceptorInterferon-Stimulated Gene Factor 3Interleukin-15Interleukin-15 Receptor alpha SubunitKiller Cells, NaturalLymphocyte DepletionLymphoid TissueLymphomaLymphopoiesisMiceMice, Inbred C57BLgamma interferon activation factorInterferon gamma ReceptorInterferon-Stimulated Gene Factor 3Interleukin-15Interleukin-15 Receptor alpha SubunitProtein IsoformsReceptors, InterferonStat1 protein, mouseSTAT1 Transcription FactorIL-15RαinterferonisoformsMHC class INK cellssignal transduction

Identifiers

PMID33042133
PMCPMC7519029
OpenAlexW3086537988

What OpenQuestion holds

Textmetadata
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.