DINURU

The Synthesis and Evaluation of Organometallic Dinuclear Ruthenium Complexes as Anti-Cancer Drugs

 Coordinatore ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE 

 Organization address address: BATIMENT CE 3316 STATION 1
city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Paul Joseph
Cognome: Dyson
Email: send email
Telefono: +41 21 693 98 54
Fax: +41 21 693 97 80

 Nazionalità Coordinatore Switzerland [CH]
 Totale costo 178˙601 €
 EC contributo 178˙601 €
 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-2010-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-07-01   -   2013-06-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE

 Organization address address: BATIMENT CE 3316 STATION 1
city: LAUSANNE
postcode: 1015

contact info
Titolo: Prof.
Nome: Paul Joseph
Cognome: Dyson
Email: send email
Telefono: +41 21 693 98 54
Fax: +41 21 693 97 80

CH (LAUSANNE) coordinator 178˙601.60

Mappa


 Word cloud

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

expertise    cancer    anti    complexes    candidate    influence    skills    drugs    he    gain    analytical    ruthenium    interactions    independent    biomolecular    resistance    toxicity   

 Obiettivo del progetto (Objective)

'Current platinum-based anti-cancer drugs, such as cisplatin, are well established in the successful treatment of various forms of cancer, however, the use of these drugs is significantly limited by associated side effects and drug resistance. Ruthenium-based alternatives, some of which are in clinical testing, have shown considerable promise, exhibiting low general toxicity alongside selectivity and high activity toward cancerous tissue.

This proposal takes advantage of these remarkable properties in the design, synthesis and evaluation of novel dinuclear ruthenium-based anti-cancer drugs. These complexes will contain two ruthenium moieties linked by an organic tether – the structure of which will have a major influence on the conformation of the complexes and will therefore influence their interactions with biomolecular targets. The relationship between complex structures and their anti-cancer properties will be studied and their biomolecular targets identified, allowing the rational development of more potent anti-cancer drugs that express their activity by non-DNA damaging modes of action – essential in overcoming the toxicity and resistance problems of established metal complexes.

To achieve these objectives the candidate will build upon his experience in synthetic and analytical chemistry to isolate and characterize the complexes; he will develop expertise in bio-analytical techniques to allow him to identify their biomolecular targets and evaluate complex-biomolecule interactions/reactivity to probe their biological mode of anti-cancer activity.

Through this project the candidate will gain substantial new expertise in biochemistry, proteomics and advanced mass spectrometry. He will gain experience in the management and coordination of an independent project whilst developing scientific and complementary skills, such as leadership qualities and teaching skills - essential in his development as a promising independent researcher.'

Altri progetti dello stesso programma (FP7-PEOPLE)

ENGCABRA (2011)

Biomedical engineering for cancer and brain disease diagnosis and therapy development

Read More  

CHEMPROT-HLMS (2013)

Chemical proteomics for universal profiling of histone lysine malonylation and succinylation

Read More  

POLYPTERUS EVO-DEVO (2008)

Polypterids – development and evolution of a ’living fossil’

Read More