Evidence map›Paper›PMID 21868762›Full record

ReviewClinical cancer research : an official journal of the American Association for Cancer Research2011

MALT1 protease: a new therapeutic target in B lymphoma and beyond?

Linda M McAllister-Lucas, Mathijs Baens, Peter C Lucas

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical cancer research : an official journal of the American Association for Cancer Research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  7. Review
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  11. Targeted deep sequencing of gastric marginal zone lymphoma identified alterations of TRAF3 and TNFAIP3 that were mutually exclusive for MALT1 rearrangement.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2018
    Article
  12. Article
  13. Review
  14. Article
  15. Molecular Pathogenesis of MALT Lymphoma.Gastroenterology research and practice · 2015
    Review
  16. Review
  17. Review
  18. Review
  19. Review
  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

3 authors at 3 institutions in 2 countries.

Linda M McAllister-LucasDepartment of Pediatrics and Communicable Diseases, University of Michigan, Ann Arbor, Michigan 48109, USA. lindaluc@umich.edu
Mathijs Baens
Peter C Lucas
Center for Human Genetics · USUniversity of Michigan–Ann Arbor · USVlaams Instituut voor Biotechnologie · BE

Funding

GPCR Signaling Through a Novel NF-kB PathwayR01HL082914 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LUCAS, PETER C, MCALLISTER-LUCAS, LINDA M · 2008 to 2017
$3.6M
Novel signal pathway mediating Hypertension/Obesity-dependent Insulin ResistanceR01DK079973 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LUCAS, PETER C · 2009 to 2013
$1.6M
Multiple Roles of the API2 Moiety in API2-MALT1-Mediated LymphomagenesisR01CA124540 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MCALLISTER-LUCAS, LINDA M · 2008 to 2012
$1.6M
NCI NIH HHS R01 CA124540NCI NIH HHS R01CA124540NHLBI NIH HHS R01 HL082914NHLBI NIH HHS R01HL082914NIDDK NIH HHS R01 DK079973NIDDK NIH HHS R01DK079973
6 · The paper itself

Abstract

The identification of mucosa-associated lymphoid tissue lymphoma translocation 1 (MALT1) as a gene that is perturbed in the B-cell neoplasm MALT lymphoma, already more than a decade ago, was the starting point for an intense area of research. The fascination with MALT1 was fueled further by the observation that it contains a domain homologous to the catalytic domain of caspases and thus, potentially, could function as a protease. Discoveries since then initially revealed that MALT1 is a key adaptor molecule in antigen receptor signaling to the transcription factor NF-κB, which is crucial for lymphocyte function. However, recent discoveries show that this function of MALT1 is not restricted to lymphocytes, witnessed by the ever-increasing list of receptors from cells within and outside of the immune system that require MALT1 for NF-κB activation. Yet, a role for MALT1 protease activity was shown only recently in immune signaling, and its importance was then further strengthened by the dependency of NF-κB-addicted B-cell lymphomas on this proteolytic activity. Therapeutic targeting of MALT1 protease activity might, therefore, become a useful approach for the treatment of these lymphomas and, additionally, an effective strategy for treating other neoplastic and inflammatory disorders associated with deregulated NF-κB signaling.

Indexed as

Caspase InhibitorsAnimalsCaspasesGene Knockout TechniquesHumansLymphoma, B-Cell, Marginal ZoneMolecular Targeted TherapyMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinNeoplasm ProteinsProtease InhibitorsCaspase InhibitorsCaspasesMALT1 protein, humanMucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 ProteinNeoplasm ProteinsProtease Inhibitors

Identifiers

PMID21868762
PMCPMC3207008
OpenAlexW2054451394

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.