About the VHIR
Here at the Vall d'Hebron Research Institute (VHIR) we promote biomedical research, innovation and teaching. Over 1,800 people are seeking to understand diseases today so the treatment can be improved tomorrow.
Research
We are working to understand diseases, to find out how they operate and to create better treatments for patients. Get to know about our groups and their lines of research.
People
People are the centre of the Vall d'Hebron Research Institute (VHIR). This is why we are bound by the principles of freedom of research, gender equality and professional attitudes that HRS4R promotes.
Clinical trials
Our work is not just basic or translational; we are leaders in clinical research. Enter and find about the clinical trials we are conducting and why we are a world reference in this field.
Progress
Our aim is to make the research carried out at the Vall d’Hebron Research Institute (VHIR) a driving force for transformation. How? By identifying new channels and solutions for the promotion of people's health and well-being.
Core facilities
We offer specialist support for researchers, internal and external alike, ranging from specific services to preparing complete projects. All this, from a perspective of quality and speed of response.
News
We offer you a gateway for staying up to date on everything going on at the Vall d’Hebron Research Institute (VHIR), from the latest news to future solidarity activities and initiatives that we are organising.
Speaker: Marta Barber Servera, predoctoral Researcher, Cancer Laboratory/Biomedical Research Group in Urology (VHIR).
Aurora Borealis (BORA) is the major activator of the mitotic kinase polo-like kinase 1 (PLK1). Both proteins are known to have an oncogenic role in the tumorigenesis and progression of ovarian cancer (OC). OC is a very aggressive tumor type usually diagnosed at advanced stages where the survival is very low and there are not targeted therapies. Our project aims to decipher the mechanisms by which BORA enhances OC aggressiveness, and also to validate BORA as a potential therapeutic target for OC. Our results indicate that BORA overexpression increases, through PLK1 activation, the expression of genes involved in epithelial-mesenchymal transition (EMT), resulting in higher migration and invasive capacities in vitro and faster metastasis formation in vivo. By contrast, BORA downregulation reduces OC cell viability in vitro and ex vivo, both as a single treatment and in combination with the standard of care (cisplatin/paclitaxel). Altogether, our results uncovered a potential new role of BORA in OC metastasis through the induction of EMT. Moreover, we demonstrated that targeting BORA with RNA-based nanotherapies reduces OC cell viability, providing a potential therapeutic opportunity for OC management.
Marta Barber Servera, predoctoral Researcher in Cell Cycle and Cancer Laboratory/Biomedical Research Group in Urology (VHIR), led by Dr. Juan Morote and Dra. Anna Santamaria (thesis supervisor). Graduated in Biomedical Science by the Universitat Autonoma de Barcelona and in the Translational Biomedical Research Master (VHIR).
Host: Dr. Olga Méndez Fernández, Postdoctoral researcher Biomedical Research in Urology (VHIR)