Evidence map›Paper›PMID 21074722›Full record

ArticleDevelopmental cell2010

The NF2 tumor suppressor, Merlin, regulates epidermal development through the establishment of a junctional polarity complex.

Andrew B Gladden, Alan M Hebert, Eveline E Schneeberger, Andrea I McClatchey

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

117 citing papers in PubMed, 169 citations in OpenAlex.

  1. Nf2 orchestrates β-arrestin2-biased PTH1R signaling to couple bone mass with skeletal integrity.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Cell proliferation and differentiation during epidermis renewal.Journal of Zhejiang University. Science. B · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. The molecular biology of NF2/Merlin on tumorigenesis and development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review

57 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

4 authors at 2 institutions in 1 country.

Andrew B GladdenMassachusetts General Hospital Cancer Center, Charlestown, MA 02129, USA.
Alan M Hebert
Eveline E Schneeberger
Andrea I McClatchey
Harvard University · USMassachusetts General Hospital · US

Funding

IMMUNE FUNCTIONS OF ACCESSORY CELLS IN THE LUNGR01HL036781 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SCHNEEBERGER, EVELINE ELSA · 1986 to 2011
$4.5M
Molecular Function of the Nf2 Tumor Suppressor, MerlinR01CA113733 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI MCCLATCHEY, ANDREA I · 2005 to 2014
$3.1M
Functional analysis of ERM proteins in epithelial morphogenesisR01GM087558 · NIGMS · UNIVERSITY OF CHICAGO · PI FEHON, RICHARD G, MCCLATCHEY, ANDREA I · 2010 to 2013
$1.9M
Stem Cell Regulation by the NF2 Tumor Suppressor MerlinF32CA124030 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI GLADDEN, ANDREW B. · 2006 to 2008
$139k
NCI NIH HHS 5F32CA124030NCI NIH HHS F32 CA124030NCI NIH HHS R01 CA113733NCI NIH HHS R01CA113733NHLBI NIH HHS R01 HL036781NIGMS NIH HHS R01 GM087558
6 · The paper itself

Abstract

The neurofibromatosis type 2 (NF2) tumor suppressor, Merlin, is a FERM (Four point one, Ezrin, Radixin, Moesin) domain-containing protein whose loss results in defective morphogenesis and tumorigenesis in multiple tissues. Like the closely related ERM proteins (Ezrin, Radixin, and Moesin), Merlin may organize the plasma membrane by assembling membrane protein complexes and linking them to the cortical actin cytoskeleton. We previously found that Merlin is a critical mediator of contact-dependent inhibition of proliferation and is required for the establishment of stable adherens junctions (AJs) in cultured cells. Here, we delineate the molecular function of Merlin in AJ establishment in epidermal keratinocytes in vitro and confirm that a role in AJ establishment is an essential function of Merlin in vivo. Our studies reveal that Merlin can associate directly with α-catenin and link it to Par3, thereby providing an essential link between the AJ and the Par3 polarity complex during junctional maturation.

Indexed as

Cell PolarityAdaptor Proteins, Signal TransducingAdherens Junctionsalpha CateninAnimalsCell Adhesion MoleculesCell Cycle ProteinsEpidermal CellsEpidermisKeratinocytesMiceMice, TransgenicNeurofibromatosis 2Neurofibromin 2Recombinant Fusion ProteinsAdaptor Proteins, Signal Transducingalpha CateninCell Adhesion MoleculesCell Cycle ProteinsNeurofibromin 2Pard3 protein, mouseRecombinant Fusion Proteins

Identifiers

PMID21074722
PMCPMC3033574
OpenAlexW2015155360

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.