Targeting stromal cells to modify tumor mechanical microenvironment and optimize...
Targeting stromal cells to modify tumor mechanical microenvironment and optimize drug delivery
Current chemotherapeutic agents are potent enough to kill cancer cells. Nonetheless, failure of standard chemotherapies for many cancer types (e.g., pancreatic and breast cancers) is primarily attributed to these agents never reac...
ver más
¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video
Proyectos interesantes
CAFTECH
Unraveling the therapeutic potential of cancer associated fi...
50K€
Cerrado
MYO-DESMOPLASIA
Modulating the behaviour of cancer myofibroblasts to control...
164K€
Cerrado
antiCAFing
Harnessing Stromal Fibroblasts to Reduce Resistance and Impr...
2M€
Cerrado
ReEngineeringCancer
Re engineering the tumor microenvironment to alleviate mecha...
1M€
Cerrado
MetCAF
Uncovering the Role of Cancer Associated Fibroblasts in Faci...
1M€
Cerrado
De-CAF
Decoding local crosstalk in tumor formation
184K€
Cerrado
Información proyecto STROMAMECH
Duración del proyecto: 25 meses
Fecha Inicio: 2015-03-03
Fecha Fin: 2017-04-30
Líder del proyecto
UNIVERSITY OF CYPRUS
No se ha especificado una descripción o un objeto social para esta compañía.
TRL
4-5
Presupuesto del proyecto
152K€
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
Current chemotherapeutic agents are potent enough to kill cancer cells. Nonetheless, failure of standard chemotherapies for many cancer types (e.g., pancreatic and breast cancers) is primarily attributed to these agents never reaching cancer cells in amounts sufficient for complete cure. In solid tumours, blood vessels are often compressed, drastically reducing perfusion, thus resulting in insufficient drug delivery. Vessel compression is a consequence of mechanical stresses accumulated within the tumour during progression. Alleviation of these stresses has the potential to reopen compressed vessels and improve tumour perfusion. Here, the applicant proposes to test the hypothesis that judicious depletion of stromal cells, namely the cancer-associated fibroblasts (CAFs), has the potential to alleviate stress levels in highly desmoplastic and hypoperfused tumours and, thus, enhance chemotherapy. To explore this hypothesis, a combination of cutting-edge computational and experimental techniques will be employed. Specifically, a structure-based biomechanical model will be developed to analyse the contribution of CAFs to the generation and transmission of forces within a tumour. Subsequently, in vivo studies will be performed in mice to validate model predictions and identify the degree of CAF depletion that optimizes the efficacy of treatment. Successful completion of the proposed research will reveal the role of CAFs on the biomechanical behaviour of tumours and contribute to developing a therapeutic strategy for treatment of hypovascular tumours. Therefore, the proposal negotiates a subject of considerable importance for European society and beyond. Furthermore, the proposed research and training will establish a bidirectional transfer of skills where the applicant’s expertise in cell mechanics will be complemented by the Host’s in cancer biophysics, thus enhancing the applicant’s scientific potential and professional maturity, and promoting European research.