Evidence map›Paper›PMID 21402876›Full record

ArticleJournal of cell science2011

Trp53 regulates Notch 4 signaling through Mdm2.

Youping Sun, Malgorzata Klauzinska, Robert J Lake, Joseph M Lee, Stefania Santopietro, Ahmed Raafat, David Salomon, Robert Callahan, Spyros Artavanis-Tsakonas

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cell science, 2011. 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
1.7field-weighted citation impact, top 16% 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, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Decoding the PTM-switchboard of Notch.Biochimica et biophysica acta. Molecular cell research · 2019
    Review
  5. Classifying tumors by supervised network propagation.Bioinformatics (Oxford, England) · 2018
    Article
  6. Article
  7. Article
  8. Article
  9. Notch Signaling in Neuroendocrine Tumors.Frontiers in oncology · 2016
    Review
  10. Article
  11. Article
  12. MDM2's social network.Oncogene · 2014
    Review
  13. Article
  14. Article
  15. Ubiquitinations in the notch signaling pathway.International journal of molecular sciences · 2013
    Article
  16. Article
  17. Hypo- and hyperactivated Notch signaling induce a glycolytic switch through distinct mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2011
    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

9 authors at 5 institutions in 2 countries.

Youping SunDepartment of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Malgorzata Klauzinska
Robert J Lake
Joseph M Lee
Stefania Santopietro
Ahmed Raafat
David Salomon
Robert Callahan
Spyros Artavanis-Tsakonas
Center for Cancer Research · USNational Institutes of Health · USHarvard University · USInstitut Curie · FRUniversity of Pennsylvania · US

Funding

Mammary Tumorigenesis in Inbred and Feral MiceZIABC005148 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CALLAHAN, ROBERT · 2009 to 2015
$7.7M
Cell Interactions Controlling Neural DifferentiationR37NS026084 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ARTAVANIS-TSAKONAS, SPYRIDON · 2004 to 2010
$4.2M
Notch Signaling in Mammary Development and TumorigenesisR01CA098402 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI ARTAVANIS-TSAKONAS, SPYRIDON · 2003 to 2013
$3.6M
CELL INTERACTIONS CONTROLLING NEURAL DIFFERENTIATIONR01NS026084 · NINDS · YALE UNIVERSITY · PI ARTAVANIS-TSAKONAS, SPYRIDON · 1988 to 2003
$839k
Intramural NIH HHSNCI NIH HHS CA098402NCI NIH HHS R01 CA098402NINDS NIH HHS NS26084NINDS NIH HHS R01 NS026084NINDS NIH HHS R37 NS026084
6 · The paper itself

Abstract

Notch receptors and their ligands have crucial roles in development and tumorigenesis. We present evidence demonstrating the existence of an antagonistic relationship between Notch 4 and Trp53, which is controlled by the Mdm2-dependent ubiquitylation and degradation of the Notch receptor. We show that this signal-controlling mechanism is mediated by physical interactions between Mdm2 and Notch 4 and suggest the existence of a trimeric complex between Trp53, Notch 4 and Mdm2, which ultimately regulates Notch activity. Functional studies indicate that Trp53 can suppress NICD4-induced anchorage-independent growth in mammary epithelial cells and present evidence showing that Trp53 has a pivotal role in the suppression of Notch-associated tumorigenesis in the mammary gland.

Indexed as

Signal TransductionAnimalsCell LineEpithelial CellsHumansMiceProtein BindingProtein Structure, TertiaryProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2Receptor, Notch4Receptors, NotchTumor Suppressor Protein p53Mdm2 protein, mouseNOTCH4 protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2Receptor, Notch4Receptors, NotchTumor Suppressor Protein p53

Identifiers

PMID21402876
PMCPMC3056605
OpenAlexW2031350022

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.