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Contact-dependent inhibition of EGFR signaling by Nf2/Merlin

The neurofibromatosis type 2 (NF2) tumor suppressor, Merlin, is a membrane/cytoskeleton-associated protein that mediates contact-dependent inhibition of proliferation. Here we show that upon cell–cell contact Merlin coordinates the processes of adherens junction stabilization and negative regulation...

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Autores principales: Curto, Marcello, Cole, Banumathi K., Lallemand, Dominique, Liu, Ching-Hui, McClatchey, Andrea I.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064288/
https://www.ncbi.nlm.nih.gov/pubmed/17548515
http://dx.doi.org/10.1083/jcb.200703010
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author Curto, Marcello
Cole, Banumathi K.
Lallemand, Dominique
Liu, Ching-Hui
McClatchey, Andrea I.
author_facet Curto, Marcello
Cole, Banumathi K.
Lallemand, Dominique
Liu, Ching-Hui
McClatchey, Andrea I.
author_sort Curto, Marcello
collection PubMed
description The neurofibromatosis type 2 (NF2) tumor suppressor, Merlin, is a membrane/cytoskeleton-associated protein that mediates contact-dependent inhibition of proliferation. Here we show that upon cell–cell contact Merlin coordinates the processes of adherens junction stabilization and negative regulation of epidermal growth factor receptor (EGFR) signaling by restraining the EGFR into a membrane compartment from which it can neither signal nor be internalized. In confluent Nf2 (−/−) cells, EGFR activation persists, driving continued proliferation that is halted by specific EGFR inhibitors. These studies define a new mechanism of tumor suppression, provide mechanistic insight into the poorly understood phenomenon of contact-dependent inhibition of proliferation, and suggest a therapeutic strategy for NF2-mutant tumors.
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spelling pubmed-20642882007-12-04 Contact-dependent inhibition of EGFR signaling by Nf2/Merlin Curto, Marcello Cole, Banumathi K. Lallemand, Dominique Liu, Ching-Hui McClatchey, Andrea I. J Cell Biol Research Articles The neurofibromatosis type 2 (NF2) tumor suppressor, Merlin, is a membrane/cytoskeleton-associated protein that mediates contact-dependent inhibition of proliferation. Here we show that upon cell–cell contact Merlin coordinates the processes of adherens junction stabilization and negative regulation of epidermal growth factor receptor (EGFR) signaling by restraining the EGFR into a membrane compartment from which it can neither signal nor be internalized. In confluent Nf2 (−/−) cells, EGFR activation persists, driving continued proliferation that is halted by specific EGFR inhibitors. These studies define a new mechanism of tumor suppression, provide mechanistic insight into the poorly understood phenomenon of contact-dependent inhibition of proliferation, and suggest a therapeutic strategy for NF2-mutant tumors. The Rockefeller University Press 2007-06-04 /pmc/articles/PMC2064288/ /pubmed/17548515 http://dx.doi.org/10.1083/jcb.200703010 Text en Copyright © 2007, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Curto, Marcello
Cole, Banumathi K.
Lallemand, Dominique
Liu, Ching-Hui
McClatchey, Andrea I.
Contact-dependent inhibition of EGFR signaling by Nf2/Merlin
title Contact-dependent inhibition of EGFR signaling by Nf2/Merlin
title_full Contact-dependent inhibition of EGFR signaling by Nf2/Merlin
title_fullStr Contact-dependent inhibition of EGFR signaling by Nf2/Merlin
title_full_unstemmed Contact-dependent inhibition of EGFR signaling by Nf2/Merlin
title_short Contact-dependent inhibition of EGFR signaling by Nf2/Merlin
title_sort contact-dependent inhibition of egfr signaling by nf2/merlin
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064288/
https://www.ncbi.nlm.nih.gov/pubmed/17548515
http://dx.doi.org/10.1083/jcb.200703010
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