Evidence map›Paper›PMID 23022962›Full record

ArticleCellular signalling2013

Cripto-1 enhances the canonical Wnt/β-catenin signaling pathway by binding to LRP5 and LRP6 co-receptors.

Tadahiro Nagaoka, Hideaki Karasawa, Thomas Turbyville, Maria-Cristina Rangel, Nadia P Castro, Monica Gonzales, Alyson Baker, Masaharu Seno, Stephen Lockett, Yoshimi E Greer and 3 more

Open access · greenAbstract read
In one paragraph

Article in Cellular signalling, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

37 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. LRP5 and LRP6 in Wnt Signaling: Similarity and Divergence.Frontiers in cell and developmental biology · 2021
    Review
  7. Review
  8. CRIPTO antagonist ALK4Breast cancer research : BCR · 2020
    Article
  9. Review
  10. Review
  11. Article
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  15. Article
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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

13 authors at 3 institutions in 2 countries.

Tadahiro NagaokaTumor Growth Factor Section, Laboratory of Cancer Prevention, Frederick National Laboratory for Cancer Research, 1050 Boyles St., Bldg 560/Room 12-46, Frederick, MD 21702, USA.
Hideaki Karasawa
Thomas Turbyville
Maria-Cristina Rangel
Nadia P Castro
Monica Gonzales
Alyson Baker
Masaharu Seno
Stephen Lockett
Yoshimi E Greer
Jeffrey S Rubin
David S Salomon
Caterina Bianco
Frederick National Laboratory for Cancer Research · USCenter for Cancer Research · USOkayama University · JP

Funding

Wnt Signaling and Secreted Frizzled-Related ProteinsZIABC010251 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI RUBIN, JEFFREY · 2009 to 2014
$2.9M
CCR NIH HHS HHSN261200800001CIntramural NIH HHS Z99 CA999999NCI NIH HHS HHSN261200800001ENCI NIH HHS Y99 CA999999
6 · The paper itself

Abstract

Cripto-1 is implicated in multiple cellular events, including cell proliferation, motility and angiogenesis, through the activation of an intricate network of signaling pathways. A crosstalk between Cripto-1 and the canonical Wnt/β-catenin signaling pathway has been previously described. In fact, Cripto-1 is a downstream target gene of the canonical Wnt/β-catenin signaling pathway in the embryo and in colon cancer cells and T-cell factor (Tcf)/lymphoid enhancer factor binding sites have been identified in the promoter and the first intronic region of the mouse and human Cripto-1 genes. We now demonstrate that Cripto-1 modulates signaling through the canonical Wnt/β-catenin/Tcf pathway by binding to the Wnt co-receptors low-density lipoprotein receptor-related protein (LRP) 5 and LRP6, which facilitates Wnt3a binding to LRP5 and LRP6. Cripto-1 functionally enhances Wnt3a signaling through cytoplasmic stabilization of β-catenin and elevated β-catenin/Tcf transcriptional activation. Conversely, Wnt3a further increases Cripto-1 stimulation of migration, invasion and colony formation in soft agar of HC11 mouse mammary epithelial cells, indicating that Cripto-1 and the canonical Wnt/β-catenin signaling co-operate in regulating motility and in vitro transformation of mammary epithelial cells.

Indexed as

Wnt Signaling PathwayAnimalsbeta CateninCell LineCell MovementGPI-Linked ProteinsHEK293 CellsHumansIntercellular Signaling Peptides and ProteinsLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-6MiceNeoplasm ProteinsProtein BindingProtein Structure, TertiarySmad2 Proteinbeta CateninDkk1 protein, mouseGPI-Linked ProteinsIntercellular Signaling Peptides and ProteinsLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-6Neoplasm ProteinsSmad2 ProteinSmad3 ProteinTDGF1 protein, humanWnt3A Protein

Identifiers

PMID23022962
PMCPMC3508164
OpenAlexW2062392648

What OpenQuestion holds

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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.