Evidence map›Paper›PMID 10698525›Full record

ArticleOncogene2000

Neoplastic transformation by Notch is independent of transcriptional activation by RBP-J signalling.

E Dumont, K P Fuchs, G Bommer, B Christoph, E Kremmer, B Kempkes

Abstract read
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In one paragraph

Article in Oncogene, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

26 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Review
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  11. Non-canonical activation of Notch signaling/target genes in vertebrates.Cellular and molecular life sciences : CMLS · 2010
    Review
  12. Article
  13. Article
  14. Article
  15. Article
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  17. Article
  18. Article
  19. Review
  20. Notch signaling in mammary development and oncogenesis.Journal of mammary gland biology and neoplasia · 2004
    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

6 authors at 2 institutions in 2 countries.

E DumontInstitut für Klinische Molekularbiologie und Tumorgenetik, GSF-Forschungszentrum für Umwelt und Gesundheit, München, Germany.
K P Fuchs
G Bommer
B Christoph
E Kremmer
B Kempkes
Urologische Klinik München · DEAmt für Umwelt · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signalling through the transmembrane receptor Notch is triggered by ligand binding, which induces the proteolytic cleavage of the Notch protein. This cleavage generates an intracellular fragment of the Notch protein (Notch-IC), which translocates into the nucleus and modifies transcription of target genes through its association with the RBP-J protein. Thus, the isolated Notch-IC protein represents the constitutively activated receptor. We have performed a deletion analysis of Notch IC in order to identify the transferable transactivation domain of Notch-IC and the minimal domain of Notch-IC required for RBP-J dependent transactivational activation. Functionally, Notch-IC has been linked to cell fate decision in development and oncogenesis in vivo. In vitro, Notch-IC can cooperate in neoplastic transformation of baby rat kidney cells with the adenoviral E1A protein. We have defined the minimal domain of Notch-IC required for E1A cotransformation. This domain, consisting of the ankyrin repeats of Notch-IC only, can neither activate RBP-J dependent transcription nor does it carry a transactivation domain. Therefore, the ankyrin repeat domain of Notch-IC might trigger novel pathways relevant for transformation but unrelated to RBP-J signalling.

Indexed as

Nuclear ProteinsTranscriptional ActivationAdenovirus E1A ProteinsAnimalsCell Transformation, NeoplasticChlorocebus aethiopsCocarcinogenesisCOS CellsDNA-Binding ProteinsGene Expression RegulationGenes, SyntheticHeLa CellsHumansImmunoglobulin J Recombination Signal Sequence-Binding ProteinMembrane ProteinsMiceAdenovirus E1A ProteinsDNA-Binding ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinMembrane ProteinsNuclear ProteinsRbpjl2 protein, ratRBPJ protein, humanRbpj protein, mouseReceptors, NotchRecombinant Fusion Proteins

Identifiers

PMID10698525
OpenAlexW2023071161

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.