Evidence map›Paper›PMID 23770847›Full record

ArticleOncogene2014

The API2-MALT1 fusion exploits TNFR pathway-associated RIP1 ubiquitination to promote oncogenic NF-κB signaling.

S Rosebeck, A O Rehman, I J Apel, D Kohrt, A Appert, M A O'Donnell, A T Ting, M-Q Du, M Baens, P C Lucas and 1 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. RIPK1 binds to vitamin D receptor and decreases vitamin D-induced growth suppression.The Journal of steroid biochemistry and molecular biology · 2017
    Article
  11. Article
  12. Review
  13. Review
  14. Radical surgery may be not an optimal treatment approach for pulmonary MALT lymphoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  15. Review
  16. Review
  17. 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 4 institutions in 2 countries.

S RosebeckDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI, USA.
A O RehmanDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI, USA.
I J ApelDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
D KohrtDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI, USA.
A AppertDivision of Molecular Histopathology, Department of Pathology, University of Cambridge, Laboratory Block, Addenbrooke's Hospital, Cambridge, UK.
M A O'DonnellImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
A T TingImmunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
M-Q DuDivision of Molecular Histopathology, Department of Pathology, University of Cambridge, Laboratory Block, Addenbrooke's Hospital, Cambridge, UK.
M Baens1] Human Genome Laboratory, Molecular Genetics, Center for Human Genetics, Catholic University Leuven, Leuven, Belgium [2] Human Genome Laboratory, Department of Molecular and Developmental Genetics, Flanders Institute for Biotechnology (VIB), Leuven, Belgium.
P C LucasDepartment of Pathology, University of Michigan Medical School, Ann Arbor, MI, USA.
L M McAllister-LucasDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical School, Ann Arbor, MI, USA.
University of Michigan–Ann Arbor · USIcahn School of Medicine at Mount Sinai · USAddenbrooke's Hospital · GBUniversity of Cambridge · GB

Funding

Training Program in Molecular HematologyT32HL007622 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SUNG WON CHOI, Jordan A. Shavit · 1986 to 2026
$9.2M
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
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 T32 HL007622NHLBI NIH HHS T32-HL007622-21A2
6 · The paper itself

Abstract

The API2-MALT1 fusion oncoprotein is created by the recurrent t(11;18)(q21;q21) chromosomal translocation in mucosa-associated lymphoid tissue (MALT) lymphoma. We identified receptor interacting protein-1 (RIP1) as a novel API2-MALT1-associated protein, and demonstrate that RIP1 is required for API2-MALT1 to stimulate canonical nuclear factor kappa B (NF-κB). API2-MALT1 promotes ubiquitination of RIP1 at lysine (K) 377, which is necessary for full NF-κB activation. Furthermore, we found that TNF receptor-associated factor 2 (TRAF2) recruitment is required for API2-MALT1 to induce RIP1 ubiquitination, NF-κB activation and cellular transformation. Although both TRAF2 and RIP1 interact with the API2 moiety of API2-MALT1, this moiety alone is insufficient to induce RIP1 ubiquitination or activate NF-κB, indicating that API2-MALT1-dependent RIP1 ubiquitination represents a gain of function requiring the concerted actions of both the API2 and MALT1 moieties of the fusion. Intriguingly, constitutive RIP1 ubiquitination was recently demonstrated in several solid tumors, and now our study implicates RIP1 ubiquitination as a critical component of API2-MALT1-dependent lymphomagenesis.

Indexed as

Blotting, WesternCell Line, TumorHEK293 CellsHumansImmunoprecipitationLymphoma, B-Cell, Marginal ZoneNF-kappa BNuclear Pore Complex ProteinsOncogene Proteins, FusionOncogenesRNA-Binding ProteinsSignal TransductionTNF Receptor-Associated Factor 2TransfectionUbiquitinationAGFG1 protein, humanAPI2-MALT1 fusion protein, humanNF-kappa BNuclear Pore Complex ProteinsOncogene Proteins, FusionRNA-Binding ProteinsTNF Receptor-Associated Factor 2

Identifiers

PMID23770847
PMCPMC4237018
OpenAlexW1996738870

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.