Evidence map›Paper›PMID 29749399›Full record

ArticleLeukemia2018

Autocrine Tnf signaling favors malignant cells in myelofibrosis in a Tnfr2-dependent fashion.

William L Heaton, Anna V Senina, Anthony D Pomicter, Mohamed E Salama, Phillip M Clair, Dongqing Yan, Russell N Bell, Jeremy M Gililland, Josef T Prchal, Thomas O'Hare and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Monocyte Involvement in the Pathogenesis of Myeloproliferative Neoplasms.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. CHIP: a clonal odyssey of the bone marrow niche.The Journal of clinical investigation · 2024
    Review
  11. ANKRD22 promotes resolution of psoriasiform skin inflammation by antagonizing NIK-mediated IL-23 production.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  12. Article
  13. Article
  14. Article
  15. Haematologica · 2023
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

11 authors at 3 institutions in 1 country.

William L HeatonHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Anna V SeninaHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Anthony D PomicterHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Mohamed E SalamaARUP Laboratories, University of Utah, Salt Lake City, UT, USA.
Phillip M ClairHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Dongqing YanHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Russell N BellHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Jeremy M GilillandDepartment of Orthopaedics, University of Utah, Salt Lake City, UT, USA.
Josef T PrchalDivision of Hematology and Hematologic Malignancies, University of Utah, Salt Lake City, UT, USA.
Thomas O'HareHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.
Michael W DeiningerHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA. michael.deininger@hci.utah.edu.
University of Utah · USARUP Laboratories (United States) · USHuntsman Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor necrosis factor alpha (TNF) is increased in myelofibrosis (MF) and promotes survival of malignant over normal cells. The mechanisms altering TNF responsiveness in MF cells are unknown. We show that the proportion of marrow (BM) cells expressing TNF is increased in MF compared to controls, with the largest differential in primitive cells. Blockade of TNF receptor 2 (TNFR2), but not TNFR1, selectively inhibited colony formation by MF CD34

Indexed as

AnimalsAntigens, CDApoptosisAutocrine CommunicationHumansJanus Kinase 2MiceMice, Inbred BALB CNF-kappa BReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IISignal TransductionTumor Necrosis Factor-alphaAntigens, CDJanus Kinase 2NF-kappa BReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IITumor Necrosis Factor-alpha

Identifiers

PMID29749399
PMCPMC6224399
OpenAlexW2800519927

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.