Evidence map›Paper›PMID 16395399›Full record

ArticleThe Journal of clinical investigation2006

Delving deeper into MALT lymphoma biology.

Francesco Bertoni, Emanuele Zucca

Abstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. A Phase II Trial of the Bruton Tyrosine-Kinase Inhibitor Zanubrutinib (BGB-3111) in Patients with Relapsed/Refractory Waldenström Macroglobulinemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
  2. Review
  3. [Characteristics of Gastric Mucosa-associated Lymphoid Tissue Lymphoma in Korea].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2024
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Frontiers in microbiology · 2022
    Review
  9. Lessons to cancer from studies of leukemia and hematopoiesis.Frontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Review
  12. Clinical aspects of malt lymphomas.Current hematologic malignancy reports · 2014
    Review
  13. Article
  14. Gastric MALT lymphoma: old and new insights.Annals of gastroenterology · 2014
    Review
  15. Lymphoproliferative lung disorders: clinicopathological aspects.European respiratory review : an official journal of the European Respiratory Society · 2013
    Review
  16. The costimulatory immunogen LPS induces the B-Cell clones that infiltrate transplanted human kidneys.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  17. Article
  18. Ectopic B-cell clusters that infiltrate transplanted human kidneys are clonal.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Francesco BertoniLaboratory of Experimental Oncology and Lymphoma Unit, Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Emanuele Zucca

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucosa-associated lymphoid tissue (MALT) lymphomas can arise in a variety of extranodal sites. Interestingly, at least 3 different, apparently site-specific, chromosomal translocations, all affecting the NF-kappaB pathway, have been implicated in the development and progression of MALT lymphoma. The most common is the translocation t(11;18)(q21;q21), which results in a fusion of the cIAP2 region on chromosome 11q21 with the MALT1 gene on chromosome 18q21 and is present in more than one-third of cases. The frequency of this translocation is site-related: common in the gastrointestinal tract and lung, rare in conjunctiva and orbit, and almost absent in salivary glands, thyroid, liver, and skin. In this issue of the JCI, Hu et al. add to our understanding of the molecular consequences of this translocation, showing that its fusion product, cIAP2-MALT1, may concomitantly contribute to lymphomagenesis both as a tumor suppressor gene and as an oncogene.

Indexed as

Chromosomes, Human, Pair 11Chromosomes, Human, Pair 18Genes, Tumor SuppressorOncogenesTranslocation, GeneticCaspasesDigestive System Physiological PhenomenaGene Expression Regulation, NeoplasticGene FrequencyGene FusionHumansInhibitor of Apoptosis ProteinsLymphoma, B-Cell, Marginal ZoneMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinNeoplasm ProteinsOrgan SpecificityCaspasesInhibitor of Apoptosis ProteinsMALT1 protein, humanMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinNeoplasm Proteins

Identifiers

PMID16395399
PMCPMC1323273

What OpenQuestion holds

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Registered trials

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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.