Evidence map›Paper›PMID 23371553›Full record

ArticleScience (New York, N.Y.)2013

Phosphorylation of Dishevelled by protein kinase RIPK4 regulates Wnt signaling.

XiaoDong Huang, James C McGann, Bob Y Liu, Rami N Hannoush, Jennie R Lill, Victoria Pham, Kim Newton, Michael Kakunda, Jinfeng Liu, Christine Yu and 6 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Functions of the RIP kinase family members in the skin.Cellular and molecular life sciences : CMLS · 2023
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Deciphering the Functional Role of RIPK4 in Melanoma.International journal of molecular sciences · 2021
    Article
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

16 authors at 4 institutions in 2 countries.

XiaoDong HuangDepartment of Physiological Chemistry, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
James C McGann
Bob Y Liu
Rami N Hannoush
Jennie R Lill
Victoria Pham
Kim Newton
Michael Kakunda
Jinfeng Liu
Christine Yu
Sarah G Hymowitz
Jo-Anne Hongo
Anthony Wynshaw-Boris
Paul Polakis
Richard M Harland
Vishva M Dixit
Genesys (United States) · USInnovative Genomics Institute · USTarget (United States) · USUniversity of California, San Francisco · US

Funding

Gene Expression in Amphibian DevlopementR01GM042341 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HARLAND, RICHARD M · 1988 to 2016
$5.7M
Dishevelled-Mediated Control of Wnt/PCP PathwaysR01NS073159 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WYNSHAW-BORIS, ANTHONY J. · 2010 to 2014
$1.9M
NIGMS NIH HHS R01 GM042341NINDS NIH HHS R01 NS073159
6 · The paper itself

Abstract

Receptor-interacting protein kinase 4 (RIPK4) is required for epidermal differentiation and is mutated in Bartsocas-Papas syndrome. RIPK4 binds to protein kinase C, but its signaling mechanisms are largely unknown. Ectopic RIPK4, but not catalytically inactive or Bartsocas-Papas RIPK4 mutants, induced accumulation of cytosolic β-catenin and a transcriptional program similar to that caused by Wnt3a. In Xenopus embryos, Ripk4 synergized with coexpressed Xwnt8, whereas Ripk4 morpholinos or catalytic inactive Ripk4 antagonized Wnt signaling. RIPK4 interacted constitutively with the adaptor protein DVL2 and, after Wnt3a stimulation, with the co-receptor LRP6. Phosphorylation of DVL2 by RIPK4 favored canonical Wnt signaling. Wnt-dependent growth of xenografted human tumor cells was suppressed by RIPK4 knockdown, suggesting that RIPK4 overexpression may contribute to the growth of certain tumor types.

Indexed as

Wnt Signaling PathwayAdaptor Proteins, Signal TransducingAnimalsbeta CateninCell LineCell Line, TumorCytosolDishevelled ProteinsFemaleGene Knockdown TechniquesHEK293 CellsHumansLow Density Lipoprotein Receptor-Related Protein-6NeoplasmsNeoplasm TransplantationOvarian NeoplasmsAdaptor Proteins, Signal Transducingbeta CateninDishevelled ProteinsDVL2 protein, humanLow Density Lipoprotein Receptor-Related Protein-6LRP6 protein, humanPhosphoproteinsProtein Serine-Threonine KinasesRIPK4 protein, humanWnt3A ProteinXenopus Proteins

Identifiers

PMID23371553
PMCPMC4094295
OpenAlexW2067704394

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.