Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2000-8-2
pubmed:abstractText
Loss of the tumour-suppressor gene TSC1 is responsible for hamartoma development in tuberous sclerosis complex (TSC), which renders several organs susceptible to benign tumours. Hamartin, the protein encoded by TSC1, contains a coiled-coil domain and is expressed in most adult tissues, although its function is unknown. Here we show that hamartin interacts with the ezrin-radixin-moesin (ERM) family of actin-binding proteins. Inhibition of hamartin function in cells containing focal adhesions results in loss of adhesion to the cell substrate, whereas overexpression of hamartin in cells lacking focal adhesions results in activation of the small GTP-binding protein Rho, assembly of actin stress fibres and formation of focal adhesions. Interaction of endogenous hamartin with ERM-family proteins is required for activation of Rho by serum or by lysophosphatidic acid (LPA). Our data indicate that disruption of adhesion to the cell matrix through loss of hamartin may initiate the development of TSC hamartomas and that a Rho-mediated signalling pathway regulating cell adhesion may constitute a rate-limiting step in tumour formation.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Actins, http://linkedlifedata.com/resource/pubmed/chemical/Blood Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lysophospholipids, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Microfilament Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/ezrin, http://linkedlifedata.com/resource/pubmed/chemical/moesin, http://linkedlifedata.com/resource/pubmed/chemical/radixin, http://linkedlifedata.com/resource/pubmed/chemical/rho GTP-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/tuberous sclerosis complex 1 protein
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1465-7392
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
281-7
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:10806479-3T3 Cells, pubmed-meshheading:10806479-Actins, pubmed-meshheading:10806479-Animals, pubmed-meshheading:10806479-Blood Proteins, pubmed-meshheading:10806479-Cell Adhesion, pubmed-meshheading:10806479-Cytoskeletal Proteins, pubmed-meshheading:10806479-Endothelium, Vascular, pubmed-meshheading:10806479-Enzyme Activation, pubmed-meshheading:10806479-Genes, Tumor Suppressor, pubmed-meshheading:10806479-Humans, pubmed-meshheading:10806479-Lysophospholipids, pubmed-meshheading:10806479-Membrane Proteins, pubmed-meshheading:10806479-Mice, pubmed-meshheading:10806479-Microfilament Proteins, pubmed-meshheading:10806479-Peptide Fragments, pubmed-meshheading:10806479-Phosphoproteins, pubmed-meshheading:10806479-Proteins, pubmed-meshheading:10806479-Signal Transduction, pubmed-meshheading:10806479-Stress, Mechanical, pubmed-meshheading:10806479-Tumor Suppressor Proteins, pubmed-meshheading:10806479-Two-Hybrid System Techniques, pubmed-meshheading:10806479-Umbilical Veins, pubmed-meshheading:10806479-rho GTP-Binding Proteins
pubmed:year
2000
pubmed:articleTitle
The TSC1 tumour suppressor hamartin regulates cell adhesion through ERM proteins and the GTPase Rho.
pubmed:affiliation
MRC Laboratory for Molecular Cell Biology and Department of Biochemistry, University College London, UK. r.lamb@ucl.ac.uk
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't