RARBETA2 IN OSCC

Understanding the functional role of Retinoic Acid Receptor Beta2 in the development of oral cancer

Coordinatore	THE UNIVERSITY OF SHEFFIELD    more  Organization address address: FIRTH COURT WESTERN BANK city: SHEFFIELD postcode: S10 2TN contact info Titolo: Mrs. Nome: Joanne Cognome: Watson Email: send email Telefono: +44 114 222 4754 Fax: +44 114 222 1455
Nazionalità Coordinatore	United Kingdom [UK]
Totale costo	309˙235 €
EC contributo	309˙235 €
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-2012-IIF
Funding Scheme	MC-IIF
Anno di inizio	2013
Periodo (anno-mese-giorno)	2013-10-15   -   2015-10-14

 Partecipanti

#	participant	country	role	EC contrib. [€]
1	THE UNIVERSITY OF SHEFFIELD  Organization address address: FIRTH COURT WESTERN BANK city: SHEFFIELD postcode: S10 2TN contact info Titolo: Mrs. Nome: Joanne Cognome: Watson Email: send email Telefono: +44 114 222 4754 Fax: +44 114 222 1455	UK (SHEFFIELD)	coordinator	309˙235.20

Mappa

 Word cloud

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

 Obiettivo del progetto (Objective)

'The most common cancer in India is oral squamous cell carcinoma (OSCC), a tumour with poor survival whose incidence has also markedly increased in the UK over the past 30 years. There has been much interest in chemoprevention of OSCC, but large clinical trials of agents such as Vitamin A analogues (retinoids) have proved disappointing. One reason is that the function of retinoids in precancerous/cancerous oral tissues is poorly understood and this is a hindrance to individualisation of therapy. It is known that expression of the retinoid receptor RARbeta2 is lost as OSCC develops and we have compelling evidence that this is due to a novel role in replicative senescence, an in-built cell division limit, which functions as an anticancer system. We have a unique panel of cells from all stages of OSCC development, some which undergo replicative senescence and others which are immortal. These cells differ in their expression of RARbeta2 and are the ideal system in which to investigate the function of this receptor. We will manipulate expression of RARbeta2 in these cells and assess the effects on senescence, proliferation, apoptosis and differentiation and generate a transcriptional network. To assess these changes in a more physiological environment we will label these manipulated cells and use them in to construct tissue engineered oral mucosa, with real time quantification of the effects of retinoids and alterations in receptor expression. We will compare these results with the pattern of RARbeta2 expression in a panel of precancerous oral lesions which may allow us to identify retinoid-sensitive lesions which are amenable to retinoid therapy. This is a timely and exciting project at the basic science/clinical interface, bringing together a rising star of Indian Oral Pathology and an international centre of excellence in OSCC research. The mobility offered by this fellowship will facilitate key collaborations and knowledge transfer between India and the EU.'