Evidence map›Paper›PMID 22608498›Full record

ArticleImmunity2012

Gene deregulation and chronic activation in natural killer cells deficient in the transcription factor ETS1.

Kevin Ramirez, Katherine J Chandler, Christina Spaulding, Sasan Zandi, Mikael Sigvardsson, Barbara J Graves, Barbara L Kee

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

86 citing papers in PubMed, 131 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. ETS1 Function in Leukemia and Lymphoma.Advances in experimental medicine and biology · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Temporal Expression of Transcription FactorACS synthetic biology · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review

26 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

7 authors at 3 institutions in 2 countries.

Kevin RamirezCommittee on Immunology, The University of Chicago, Chicago, IL 60615, USA.
Katherine J Chandler
Christina Spaulding
Sasan Zandi
Mikael Sigvardsson
Barbara J Graves
Barbara L Kee
University of Chicago · USLinköping University · SEUniversity of Utah · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007090 · NIAID · UNIVERSITY OF CHICAGO · PI Peter Aidan Savage · 1985 to 2026
$11.7M
Transcriptional Control Mechanisms by ETS FactorsR01GM038663 · NIGMS · UNIVERSITY OF UTAH · PI GRAVES, BARBARA J · 1992 to 2015
$3.9M
Regulation of Lymphocyte Development by HLH ProteinsR01CA099978 · NCI · UNIVERSITY OF CHICAGO · PI KEE, BARBARA L. · 2003 to 2012
$3.2M
RETROVIRAL TRANSCRIPTIONAL CONTROL MECHANISMSR29GM038663 · NIGMS · UNIVERSITY OF UTAH · PI GRAVES, BARBARA J · 1987 to 1991
–
NCI NIH HHS CA099978NCI NIH HHS CA099978-SNCI NIH HHS CA42014NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA099978NIAID NIH HHS T32 AI007090NIAID NIH HHS T32AI007090NIGMS NIH HHS GM38663NIGMS NIH HHS R01 GM038663
6 · The paper itself

Abstract

Multiple transcription factors guide the development of mature functional natural killer (NK) cells, yet little is known about their function. We used global gene expression and genome-wide binding analyses combined with developmental and functional studies to unveil three roles for the ETS1 transcription factor in NK cells. ETS1 functions at the earliest stages of NK cell development to promote expression of critical transcriptional regulators including T-BET and ID2, NK cell receptors (NKRs) including NKp46, Ly49H, and Ly49D, and signaling molecules essential for NKR function. As a consequence, Ets1(-/-) NK cells fail to degranulate after stimulation through activating NKRs. Nonetheless, these cells are hyperresponsive to cytokines and have characteristics of chronic stimulation including increased expression of inhibitory NKRs and multiple activation-associated genes. Therefore, ETS1 regulates a broad gene expression program in NK cells that promotes target cell recognition while limiting cytokine-driven activation.

Indexed as

Amino Acid MotifsAnimalsBinding SitesCD4-Positive T-LymphocytesCells, CulturedGene Expression RegulationInhibitor of Differentiation Protein 2Interleukin-15Intracellular Signaling Peptides and ProteinsKiller Cells, NaturalLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMolecular Sequence DataProto-Oncogene Protein c-ets-1Ets1 protein, mouseIdb2 protein, mouseInhibitor of Differentiation Protein 2Interleukin-15Intracellular Signaling Peptides and ProteinsProto-Oncogene Protein c-ets-1Receptors, Natural Killer CellT-bet Transcription FactorT-Box Domain ProteinsTranscription Factors

Identifiers

PMID22608498
PMCPMC3389314
OpenAlexW2065201368

What OpenQuestion holds

Textmetadata
LicenceTDM
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.