Evidence map›Paper›PMID 17405906›Full record

ArticleBlood2007

NF-kappaB2 mutation targets TRAF1 to induce lymphomagenesis.

Baochun Zhang, Zhe Wang, Tai Li, Erdyni N Tsitsikov, Han-Fei Ding

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Origin of the Functional Distinctiveness of NF-κB/p52.Frontiers in cell and developmental biology · 2021
    Review
  6. Review
  7. Article
  8. Gene regulation and suppression of type I interferon signaling by STAT3 in diffuse large B cell lymphoma.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  9. TRAF1 Signaling in Human Health and Disease.Frontiers in immunology · 2018
    Review
  10. Review
  11. Review
  12. Prognostic Significance of TNFR-Associated Factor 1 and 2 (TRAF1 and TRAF2) in Glioblastoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

5 authors at 2 institutions in 1 country.

Baochun ZhangDepartment of Biochemistry and Cancer Biology, University of Toledo Health Science Campus, Toledo, OH 43614, USA.
Zhe Wang
Tai Li
Erdyni N Tsitsikov
Han-Fei Ding
University of Toledo · USHarvard University · US

Funding

The Tumor Suppression Potential of NF-kappaB2 p100R01CA106550 · NCI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI DING, HAN-FEI · 2005 to 2008
$907k
NCI NIH HHS CA106550NCI NIH HHS R01 CA106550
6 · The paper itself

Abstract

The NF-kappaB2 gene is recurrently mutated in human lymphoid malignancies. However, a causal relationship between NF-kappaB2 mutation and lymphomagenesis has not been established. It is also unclear how the mutation may lead to lymphoid malignancies. We report the generation of transgenic mice with targeted expression of p80HT, a lymphoma-associated NF-kappaB2 mutant, in lymphocytes. The transgenic mice display a marked expansion of peripheral B cell populations and develop predominantly small B cell lymphomas. p80HT expression has no apparent effect on the proliferation of B cells, but renders them specifically resistant to apoptosis induced by cytokine deprivation and mitogenic stimulation. Lymphocytes and lymphoma cells from p80HT mice express high levels of TRAF1, an antiapoptotic protein also implicated in lymphoid malignancies. p80HT binds the TRAF1 promoter in vivo and activates TRAF1 transcription. Moreover, TRAF1 knockdown abrogates the antiapoptotic activity of p80HT and TRAF1 deficiency reestablishes B cell homeostasis in p80HT mice. These findings demonstrate NF-kappaB2 mutation as an oncogenic event in vivo and suggest a molecular pathway for TRAF1 activation in the pathogenesis of lymphomas.

Indexed as

Mutagenesis, Site-DirectedAnimalsApoptosisCell Line, TumorCell NucleusCell SurvivalFlow CytometryHumansLymphocyte ActivationLymphocytesLymphomaMiceMice, TransgenicNF-kappa B p52 SubunitPolymerase Chain ReactionTNF Receptor-Associated Factor 2NF-kappa B p52 SubunitTNF Receptor-Associated Factor 2

Identifiers

PMID17405906
PMCPMC1924489
OpenAlexW2026387078

What OpenQuestion holds

Textmetadata
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.