Evidence map›Paper›PMID 21610251›Full record

ArticleScience signaling2011

α-catenin is a tumor suppressor that controls cell accumulation by regulating the localization and activity of the transcriptional coactivator Yap1.

Mark R Silvis, Bridget T Kreger, Wen-Hui Lien, Olga Klezovitch, G Marianna Rudakova, Fernando D Camargo, Dan M Lantz, John T Seykora, Valeri Vasioukhin

Abstract read
In one paragraph

Article in Science signaling, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 196 papers.

0numbers the graph read from it
0cells of the map it votes in
196citing papers in PubMed
15.8field-weighted citation impact, top 1% 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

196 citing papers in PubMed, 340 citations in OpenAlex.

  1. Yorkie/YAP Interactors: Fine-Tuning the Hippo Pathway Output.Cold Spring Harbor perspectives in biology · 2026
    Article
  2. Mechanobiology of the Hippo-YAP Signaling Network.Cold Spring Harbor perspectives in biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate.International journal of molecular sciences · 2024
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. MaternalFrontiers in cell and developmental biology · 2024
    Article
  18. Article
  19. Review
  20. Review

136 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

9 authors at 3 institutions in 1 country.

Mark R SilvisDivision of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Bridget T Kreger
Wen-Hui Lien
Olga Klezovitch
G Marianna Rudakova
Fernando D Camargo
Dan M Lantz
John T Seykora
Valeri Vasioukhin
Fred Hutch Cancer Center · USHarvard University · USUniversity of Washington · US

Funding

Chromosome Metabolism and Cancer Training GrantT32CA009657 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1991 to 2020
$7.6M
Cell-cell Adhesion and Signal TransductionR01CA098161 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI VASIOUKHIN, VALERI · 2003 to 2012
$3.3M
The role of srcasm in keratinocyte biologyR01AR051380 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI SEYKORA, JOHN T. · 2005 to 2009
$1.6M
Cell Polarity in Self-renewal and Differentiation of Stem/Progenitor CellsR01CA131047 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI VASIOUKHIN, VALERI · 2009 to 2012
$1.4M
NCI NIH HHS R01 CA098161NCI NIH HHS R01 CA131047NCI NIH HHS T32 CA009657NIAMS NIH HHS R01 AR051380
6 · The paper itself

Abstract

The Hippo pathway regulates contact inhibition of cell proliferation and, ultimately, organ size in diverse multicellular organisms. Inactivation of the Hippo pathway promotes nuclear localization of the transcriptional coactivator Yap1, a Hippo pathway effector, and can cause cancer. Here, we show that deletion of αE (α epithelial) catenin in the hair follicle stem cell compartment resulted in the development of skin squamous cell carcinoma in mice. Tumor formation was accelerated by simultaneous deletion of αE-catenin and the tumor suppressor-encoding gene p53. A small interfering RNA screen revealed a functional connection between αE-catenin and Yap1. By interacting with Yap1, αE-catenin promoted its cytoplasmic localization, and Yap1 showed constitutive nuclear localization in αE-catenin-null cells. We also found an inverse correlation between αE-catenin abundance and Yap1 activation in human squamous cell carcinoma tumors. These findings identify αE-catenin as a tumor suppressor that inhibits Yap1 activity and sequesters it in the cytoplasm.

Indexed as

Active Transport, Cell NucleusAdaptor Proteins, Signal Transducingalpha CateninAnimalsCarcinoma, Squamous CellCell Cycle ProteinsCell Line, TumorCell NucleusCell ProliferationHEK293 CellsHumansMiceMice, NudeMice, TransgenicPhosphoproteinsTranscription FactorsAdaptor Proteins, Signal Transducingalpha CateninCell Cycle ProteinsPhosphoproteinsTP53 protein, humanTranscription FactorsTumor Suppressor Protein p53YAP1 protein, humanYap1 protein, mouseYAP-Signaling Proteins

Identifiers

PMID21610251
PMCPMC3366274
OpenAlexW2009597834

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.