welcome
research groups
genetic services
job opportunities
seminars
contact us
   
Angiogenesis, or the formation of new blood vessels from pre-existing vasculature, is essential for tumour growth, progression and metastasis. For all these reasons, anti-angiogenic therapies have recently become a focus for research on cancer treatment. More than 50 pharmacological angiogenesis inhibitors are now at various stages of clinical investigation. Most of the targets for these compounds are factors that induce angiogenesis. One of the most important and specific is vascular endothelial growth factor (VEGF), which stimulates endothelial cell proliferation and migration, and the formation of new blood vessels. Indeed, the first selective angiogenesis inhibitor to have been approved for use in patients is Bevacizumab (Avastin), a neutralizing antibody against VEGF.

In contrast, other angiogenic factors such as transforming growth factor ß (TGFbeta) and angiopoietins induce angiogenesis through stabilization of the vasculature. Key issues in this field are to identify new molecular targets of the angiogenic cascade and to determine the exact effect of anti-angiogenic molecules in different tumour models.
To address these questions our Group of Angiogenesis in the Translational Research Laboratory, in the Institut Català d’Oncologia (ICO), Hospital Duran i Reynals are taking advantage of the joint presence of basic and clinical research in our institution. We combine basic research, designed to identify new angiogenic and anti-angiogenic pathways, with translational studies, directed toward the analysis of the clinical impact of angiogenesis inhibitors.

Basic studies:
Studies focus on the mechanisms involved in the pro-angiogenic effect of VEGF and in the stabilization of vessels by TGFbeta, looking for new genes involved in these processes in endothelial cells.
Role of the EGF receptors in angiogenesis combining endothelial cell culture and germinal tumor studies.
Angiogenic phenotype in subcutaneous tumours caused by mutations of the Ras oncogene.
Tumor invasion in transgenic mouse models of cancer.

Our translational studies are aimed at improving angiogenic therapies:
Relationship between angiogenesis and invasion in human gliomas.
Anti-angiogenesis in an orthotopic mouse model of human pancreatic tumours: Metronomic dosing of chemotherapeutic agents.
Mechanisms of resistance to anti-angiogenic therapies in animal models and human tumors.
Surrogate markers in anti-angiogenic trials.

All these studies are performed in collaboration with our clinical staff with the objective of transferring the benefits of our research to the patients with as little delay as possible.