ECAP

Genetic/epigenetic basis of ethnic differences in cancer predisposition

 Coordinatore UNIVERSITE DE LAUSANNE 

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 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 2˙495˙425 €
 EC contributo 2˙495˙425 €
 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-2013-ADG
 Funding Scheme ERC-AG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-02-01   -   2019-01-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE LAUSANNE

 Organization address city: LAUSANNE
postcode: 1015

contact info
Titolo: Ms.
Nome: Natasa
Cognome: Jovanovic
Email: send email
Telefono: +41 21 6925708
Fax: +41 21 6925705

CH (LAUSANNE) hostInstitution 2˙495˙425.00
2    UNIVERSITE DE LAUSANNE

 Organization address city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Gian-Paolo
Cognome: Dotto
Email: send email
Telefono: +41 21 6925714
Fax: +41 21 6925705

CH (LAUSANNE) hostInstitution 2˙495˙425.00

Mappa


 Word cloud

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network    genes    caucasian    epithelial    compartments    scc    clinical    fibroblasts    hypothesis       notch    skin    populations    differences    keratinocytes    differ    asian    epigenetic    capability    fibroblast    genetic    goals    basic    versus    cancer    keratinocyte    predisposition    dermal   

 Obiettivo del progetto (Objective)

'Integration of large scale genetic and epigenetic analysis needs to be coupled with well defined biological hypotheses that can be experimentally tested. This project is aimed at developing a novel integrated approach to understand genetic and epigenetic predisposition to cancer with skin as model system. The Caucasian (West European) and Asian (East Asian) populations differ substantially in their predisposition to skin cancer, specifically Squamous Cell Carcinoma (SCC). The underlying mechanisms are poorly understood. As in other organs, skin SCC results from changes in both epithelial and mesenchymal compartments. We will be focusing on two key gene regulatory networks of cells of the two compartments (keratinocytes and dermal fibroblasts), with a key role in skin SCC. The 'keratinocyte network' has Notch/p53/p63 as key nodes, while the 'dermal fibroblast network' had Notch and AP1 family members. We will pursue two main goals : 1) We will test the hypothesis that a linkage can be established between specific genetic and epigenetic marks in the Caucasian versus Asian populations and differences in expression and function of 'keratinocyte and/or dermal fibroblast network genes'. 2) We will test the hypothesis that keratinocytes and/or dermal fibroblasts of Caucasian versus Asian individuals differ in their tumor yielding capability, and that these differences in cancer forming capability are due to differences in either 'keratinocyte or dermal fibroblast network genes'. The applicant is a world leader in epithelial signaling and cancer biology, and is heading interdisciplinary research efforts that bridge the basic and clinical sciences. Together with his bioinformatician and clinician collaborators, he is in an excellent position to attain the high goals of the proposal. The approach has not been attempted before, is only possible within the frame of an advanced ERC grant, and has substantial basic as well as translational/clinical implications.'

Altri progetti dello stesso programma (FP7-IDEAS-ERC)

BIOMOF (2010)

Biomineral-inspired growth and processing of metal-organic frameworks

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PROCON (2013)

PROduction and CONsumption: Textile Economy and Urbanisation in Mediterranean Europe 1000-500 BCE

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HAMPDES (2012)

Hamiltonian PDE's and small divisor problems: a dynamical systems approach

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