Evidence map›Paper›PMID 34424918›Full record

ArticlePloS one2021

Cell-cell adhesion regulates Merlin/NF2 interaction with the PAF complex.

Anne E Roehrig, Kristina Klupsch, Juan A Oses-Prieto, Selim Chaib, Stephen Henderson, Warren Emmett, Lucy C Young, Silvia Surinova, Andreas Blees, Anett Pfeiffer and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

18 authors at 3 institutions in 2 countries.

Anne E RoehrigUCL Cancer Institute, University College London, London, United Kingdom.
Kristina KlupschUCL Cancer Institute, University College London, London, United Kingdom.
Juan A Oses-PrietoDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
Selim ChaibUCL Cancer Institute, University College London, London, United Kingdom.
Stephen HendersonUCL Cancer Institute, University College London, London, United Kingdom.
Warren EmmettUniversity College London Genetics Institute, London, United Kingdom.
Lucy C YoungUCL Cancer Institute, University College London, London, United Kingdom.
Silvia SurinovaUCL Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0003-0442-9595
Andreas BleesUCL Cancer Institute, University College London, London, United Kingdom.
Anett PfeifferUCL Cancer Institute, University College London, London, United Kingdom.
Maha TijaniUCL Cancer Institute, University College London, London, United Kingdom.
Fabian BrunkUCL Cancer Institute, University College London, London, United Kingdom.
Nicole HartigUCL Cancer Institute, University College London, London, United Kingdom.
Marta Muñoz-AlegreUCL Cancer Institute, University College London, London, United Kingdom.
Alexander HergovichUCL Cancer Institute, University College London, London, United Kingdom.
Barbara H JenningsUCL Cancer Institute, University College London, London, United Kingdom.
Alma L BurlingameDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, California, United States of America.
Pablo Rodriguez-VicianaUCL Cancer Institute, University College London, London, United Kingdom.ORCID 0000-0002-8846-543X
CRUK Lung Cancer Centre of Excellence · GBUniversity of California, San Francisco · USUniversity College London · GB

Funding

YEAST THREONINE &SERINE KINASESP41RR001614 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JULIUS, DAVID · 1985 to 2011
$24.1M
Cancer Research UKNCRR NIH HHS P41 RR001614
6 · The paper itself

Abstract

The PAF complex (PAFC) coordinates transcription elongation and mRNA processing and its CDC73/parafibromin subunit functions as a tumour suppressor. The NF2/Merlin tumour suppressor functions both at the cell cortex and nucleus and is a key mediator of contact inhibition but the molecular mechanisms remain unclear. In this study we have used affinity proteomics to identify novel Merlin interacting proteins and show that Merlin forms a complex with multiple proteins involved in RNA processing including the PAFC and the CHD1 chromatin remodeller. Tumour-derived inactivating mutations in both Merlin and the CDC73 PAFC subunit mutually disrupt their interaction and growth suppression by Merlin requires CDC73. Merlin interacts with the PAFC in a cell density-dependent manner and we identify a role for FAT cadherins in regulating the Merlin-PAFC interaction. Our results suggest that in addition to its function within the Hippo pathway, Merlin is part of a tumour suppressor network regulated by cell-cell adhesion which coordinates post-initiation steps of the transcription cycle of genes mediating contact inhibition.

Indexed as

Cell AdhesionCell ProliferationChromatinChromatin Assembly and DisassemblyContact InhibitionDNA-Binding ProteinsDNA HelicasesGene Expression RegulationHEK293 CellsHumansNeoplasmsNeurofibromin 2Protein BindingProtein Interaction MapsSignal TransductionTumor Suppressor ProteinsCDC73 protein, humanCHD1 protein, humanChromatinDNA-Binding ProteinsDNA HelicasesNeurofibromin 2Tumor Suppressor Proteins

Identifiers

PMID34424918
PMCPMC8382200
OpenAlexW3194990461

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.