TGF-BETA AND BCSCS

A study of TGF-beta effects on breast cancer stem cells

 Coordinatore CANCER RESEARCH UK 

 Organization address address: ST JOHN STREET 407 ANGEL BUILDING
city: LONDON
postcode: EC1V 4AD

contact info
Titolo: Dr.
Nome: Emma
Cognome: Ryley
Email: send email
Telefono: +44 (0) 1223 404262
Fax: +44 (0) 1223 404199

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 0 €
 EC contributo 180˙783 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-IEF-2008
 Funding Scheme MC-IEF
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-01-01   -   2011-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    CANCER RESEARCH UK

 Organization address address: ST JOHN STREET 407 ANGEL BUILDING
city: LONDON
postcode: EC1V 4AD

contact info
Titolo: Dr.
Nome: Emma
Cognome: Ryley
Email: send email
Telefono: +44 (0) 1223 404262
Fax: +44 (0) 1223 404199

UK (LONDON) coordinator 180˙783.75

Mappa

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 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

beta    mechanisms    molecular    yet    initiating    stem    capacity    cell    cscs    tumourigenic    self    cancer    tumour    progenitor    cells    tgf    breast    primary    tumours    regulation    pathway   

 Obiettivo del progetto (Objective)

'A highly tumourigenic subpopulation of cancer cells has recently been identified in primary and metastastatic breast cancer. This minority of cells termed tumour-initiating cells or “cancer stem cells“ (CSC) has been shown in several solid tumours to bear stem cell features such as the capacity to self-renew and to cause the heterogeneous lineages of cancer cells that comprise the tumour. Correlating with this, several pathways and genes required for normal stem-cell function are activated in cancer cells and play essential roles in tumourigenesis. However, the specific molecular mechanisms through which CSCs exert their tumourigenic effects remain unknown. The TGF-beta pathway is a key player in mammalian biology, and its misregulation can result in tumour development. Increasing evidences are starting to elucidate the mechanistic basis and clinical relevance of TGF-beta’s role in cancer, yet its complex and pleiotropic nature requires still a much profound understanding of the pathway. The proposed project aims to study a yet unidentified role of TGF-beta in breast cancer stem cell regulation by analyzing human breast cancer cell lines as well as fresh breast tissue samples derived from primary tumours and malignant pleural effusions from patients with breast cancer of diverse grade and stage. TGF-beta regulation of the different subtypes of breast progenitor cells will be assess by colony forming cell and mammosphere-initiating cells assays as well as by an innovative xenotransplantation assay in vitro and in vivo respectively. Moreover, a transcriptomic approach will be designed to discern the mechanisms and molecular determinants of TGF-beta's role in breast stem cell regulation. By developing this project, we will decipher how TGF-beta regulates breast stem/progenitor cell functions, paving the way for a better understanding of its complexity and therapeutic potential.'

Introduzione (Teaser)

Cancer stem cells (CSCs) are tumour cells that exhibit unique features, such as the capacity to self-renewal, differentiate, and develop resistance to anti-cancer agents, all of which have been proposed to be the cause of the overall aggressiveness of cancer metastasis. The development of specific therapies targeting specifically CSCs holds hope for improvement of survival.

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