REENGINEERINGCANCER

Re-engineering the tumor microenvironment to alleviate mechanical stresses and improve chemotherapy

 Coordinatore UNIVERSITY OF CYPRUS 

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 Nazionalità Coordinatore Cyprus [CY]
 Totale costo 1˙440˙360 €
 EC contributo 1˙440˙360 €
 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-StG
 Funding Scheme ERC-SG
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-01-01   -   2018-12-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY OF CYPRUS

 Organization address address: KALLIPOLEOS STREET 75
city: NICOSIA
postcode: 1678

contact info
Titolo: Dr.
Nome: Triantafyllos
Cognome: Stylianopoulos
Email: send email
Telefono: 35722892238
Fax: 35722894472

CY (NICOSIA) hostInstitution 1˙440˙360.00
2    UNIVERSITY OF CYPRUS

 Organization address address: KALLIPOLEOS STREET 75
city: NICOSIA
postcode: 1678

contact info
Titolo: Mrs.
Nome: Eliza
Cognome: Archeou
Email: send email
Telefono: 35722894076

CY (NICOSIA) hostInstitution 1˙440˙360.00

Mappa


 Word cloud

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drugs    stress    chemotherapy    cells    microenvironment    cancers    cancer    tumors    agents    tumor    hypothesis    stresses   

 Obiettivo del progetto (Objective)

'Current chemotherapeutic agents are potent enough to kill cancer cells. Nonetheless, failure of chemotherapies for many cancers (e.g. breast and pancreatic cancers and various sarcomas) is primarily because these agents cannot reach cancer cells in amounts sufficient to cause complete cure. The abnormal microenvironment of these tumors drastically reduces perfusion and results in insufficient delivery of therapeutic agents. Tumor structural abnormalities is in large part an effect of mechanical stresses developed within the tumor due to unchecked cancer cell proliferation that strains the tumor microenvironment. Alleviation of these stresses has the potential to normalize the tumor, enhance delivery of drugs and improve treatment efficacy. Here, I propose to test the hypothesis that re-engineering the tumor microenvironment with stress-alleviating drugs has the potential to enhance chemotherapy. To explore this hypothesis, I will make use of a mixture of cutting-edge computational and experimental techniques. I will develop sophisticated models for the biomechanical response of tumors to analyze how stresses are generated and transmitted during tumor progression. Subsequently, I will perform animal studies to validate model predictions and indentify the drug that more effectively alleviates stress levels, normalizes the tumor microenvironment and improves chemotherapy. Successful completion of this research will reveal the mechanisms for stress generation and storage in tumors and will lead to new strategies for the use of chemotherapy.'

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