CANCER SIGNALOSOMES

Spatially and temporally regulated membrane complexes in cancer cell invasion and cytokinesis

 Coordinatore TEKNOLOGIAN TUTKIMUSKESKUS VTT 

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 Nazionalità Coordinatore Finland [FI]
 Totale costo 1˙529˙369 €
 EC contributo 1˙529˙369 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2007-StG
 Funding Scheme ERC-SG
 Anno di inizio 2008
 Periodo (anno-mese-giorno) 2008-08-01   -   2013-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TURUN YLIOPISTO

 Organization address address: YLIOPISTONMAKI
city: TURUN YLIOPISTO
postcode: 20014

contact info
Titolo: Dr.
Nome: Eliisa
Cognome: Särkilahti
Email: send email
Telefono: -3335799
Fax: -3336090

FI (TURUN YLIOPISTO) beneficiary 0.00
2    TEKNOLOGIAN TUTKIMUSKESKUS VTT

 Organization address address: TEKNIIKANTIE 4 A
city: ESPOO
postcode: 02044 VTT

contact info
Titolo: Dr.
Nome: Johanna
Cognome: Ivaska
Email: send email
Telefono: +358 40 720 3971
Fax: +358 20 722 2840

FI (ESPOO) hostInstitution 0.00
3    TEKNOLOGIAN TUTKIMUSKESKUS VTT

 Organization address address: TEKNIIKANTIE 4 A
city: ESPOO
postcode: 02044 VTT

contact info
Titolo: Ms.
Nome: Jaana
Cognome: Heino
Email: send email
Telefono: -7222963
Fax: -7223161

FI (ESPOO) hostInstitution 0.00

Mappa


 Word cloud

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regulate    cells    division    cell    motility    complexes    cytoplasmic    integrin    cancer    proliferation    protein    transmembrane    signalling    progression    proteins    integrins    functions   

 Obiettivo del progetto (Objective)

'Cancer progression, characterized by uncontrolled proliferation and motility of cells, is a complex and deadly process. Integrins, a major cell surface adhesion receptor family, are transmembrane proteins known to regulate cell behaviour by transducing extracellular signals to cytoplasmic protein complexes. We and others have shown that recruitment of specific protein complexes by the cytoplasmic domains of integrins is important in tumorigenesis. Here our aim is to study three interrelated processes in cancer progression which involve integrin signalling, but which have not been elucidated earlier at all. 1) Integrins in cell division (cytokinesis). Since coordinated action of the cytoskeleton and membranes is needed both for cell division and motility, shared integrin functions can regulate both events. 2) Dynamic integrin signalosomes at the leading edge of invading cells. Spatially and temporally regulated, integrin-protein complexes at the front of infiltrating cells are likely to dictate the movement of cancer cells in tissues. 3) Transmembrane segments of integrins as scaffolds for integrin signalling. In addition to cytosolic proteins, integrins most likely interact with proteins within the membrane resulting into new signalling modalities. In this proposal we will use innovative, modern and even unconventional techniques (such as RNAi and live-cell arrays detecting integrin traffic, cell motility and multiplication, laser-microdissection, proteomics and bacterial-two-hybrid screens) to unravel these new integrin functions, for which we have preliminary evidence. Each project will give fundamentally novel mechanistic insight into the role of integrins in cancer. Moreover, these interdisciplinary new openings will increase our understanding in cancer progression in general and will open new possibilities for therapeutic intervention targeting both cancer proliferation and dissemination in the body.'

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