Evidence map›Paper›PMID 23299888›Full record

ArticleNature communications2013

Germinal centre protein HGAL promotes lymphoid hyperplasia and amyloidosis via BCR-mediated Syk activation.

Isabel Romero-Camarero, Xiaoyu Jiang, Yasodha Natkunam, Xiaoqing Lu, Carolina Vicente-Dueñas, Ines Gonzalez-Herrero, Teresa Flores, Juan Luis Garcia, George McNamara, Christian Kunder and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.3field-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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  5. Article
  6. Article
  7. Article
  8. Protein Palmitoylation in Leukocyte Signaling and Function.Frontiers in cell and developmental biology · 2020
    Review
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  10. Article
  11. The Making of Leukemia.International journal of molecular sciences · 2018
    Review
  12. Article
  13. Could Vitamin D Analogues Be Used to Target Leukemia Stem Cells?International journal of molecular sciences · 2016
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

23 authors at 8 institutions in 2 countries.

Isabel Romero-CamareroExperimental Therapeutics and Translational Oncology Program, Instituto de Biología Molecular y Celular del Cáncer, CSIC/Universidad de Salamanca, 37007 Salamanca, Spain.
Xiaoyu Jiang
Yasodha Natkunam
Xiaoqing Lu
Carolina Vicente-Dueñas
Ines Gonzalez-Herrero
Teresa Flores
Juan Luis Garcia
George McNamara
Christian Kunder
Shuchun Zhao
Victor Segura
Lorena Fontan
Jose A Martínez-Climent
Francisco Javier García-Criado
Jason D Theis
Ahmet Dogan
Elena Campos-Sánchez
Michael R Green
Ash A Alizadeh
Cesar Cobaleda
Isidro Sánchez-García
Izidore S Lossos
Stanford University · USCentro de Investigación del Cáncer · ESUniversidad de Navarra · ESUniversidad de Salamanca · ESUniversity of Miami · USCentro de Biología Molecular Severo Ochoa · ESMayo Clinic · USSylvester Comprehensive Cancer Center · US

Funding

TRIGGERING CELL DEATH IN B CELL LYMPHOMAP01CA034233 · NCI · STANFORD UNIVERSITY · PI FELSHER, DEAN W · 1985 to 2010
$19.5M
Significance and Function of HGAL in LymphomaR01CA109335 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LOSSOS, IZIDORE S · 2005 to 2013
$2.1M
Prognostic Models in Diffuse Large B-Cell LymphomaR01CA122105 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI LOSSOS, IZIDORE S · 2007 to 2010
$1.3M
NCI NIH HHS CA109335NCI NIH HHS CA122105NCI NIH HHS P01 CA034233NCI NIH HHS P01 CA34233NCI NIH HHS R01 CA109335NCI NIH HHS R01 CA122105
6 · The paper itself

Abstract

The human germinal centre-associated lymphoma gene is specifically expressed in germinal centre B-lymphocytes and germinal centre-derived B-cell lymphomas, but its function is largely unknown. Here we demonstrate that human germinal centre-associated lymphoma directly binds to Syk in B cells, increases its kinase activity on B-cell receptor stimulation and leads to enhanced activation of Syk downstream effectors. To further investigate these findings in vivo, human germinal centre-associated lymphoma transgenic mice were generated. Starting from 12 months of age these mice developed polyclonal B-cell lymphoid hyperplasia, hypergammaglobulinemia and systemic reactive amyloid A (AA) amyloidosis, leading to shortened survival. The lymphoid hyperplasia in the human germinal centre-associated lymphoma transgenic mice are likely attributable to enhanced B-cell receptor signalling as shown by increased Syk phosphorylation, ex vivo B-cell proliferation and increased RhoA activation. Overall, our study shows for the first time that the germinal centre protein human germinal centre-associated lymphoma regulates B-cell receptor signalling in B-lymphocytes which, without appropriate control, may lead to B-cell lymphoproliferation.

Indexed as

Amino Acid SequenceAmyloidosisAnimalsAntigens, LyCell ExtractsDisease Models, AnimalEnzyme ActivationGerminal CenterHumansHypergammaglobulinemiaHyperplasiaIntracellular Signaling Peptides and ProteinsIntracellular SpaceKaplan-Meier EstimateLymphoma, B-CellMembrane ProteinsAntigens, LyCell ExtractsGCSAM protein, humanIntracellular Signaling Peptides and ProteinsLy6a protein, mouseMembrane ProteinsMicrofilament ProteinsNeoplasm ProteinsProtein-Tyrosine KinasesReceptors, Antigen, B-CellrhoA GTP-Binding ProteinRNA, Small InterferingSaa2 protein, mouseSerum Amyloid A ProteinSyk KinaseSYK protein, humanSyk protein, mouse

Identifiers

PMID23299888
PMCPMC3545406
OpenAlexW1965066460

What OpenQuestion holds

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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.