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Programa de Medicina Molecular | Cardiovascular

Cardiovascular Area

José Ramón González Juanatey
Group Leader | Full Professor
jose.ramon.gonzalez.juanatey@sergas.es
 
Lab: P2L1
Área de conocimiento

The aim of the group is to contribute to identifying epigenetic modulators associated with the pathophysiology of cardiovascular diseases and their risk factors, with the aim of identifying new biomarkers and therapeutic targets that contribute to better stratification and a better approach to cardiovascular patients.

Líneas de investigación

Chemotherapy cardiotoxicity 

Breast cancer is the most prevalent in women globally. Advances in screening, early diagnosis, and therapeutic approaches in recent decades have led to a gradual increase in survival rates and life expectancy. This has highlighted the deleterious effect of long-term chemotherapy. We now know that cardiotoxicity is one of the most common complications associated with chemotherapy treatment and that cardiovascular disease is the leading cause of death among cancer survivors. Our objective is focused on the identification of new biological markers, which, together with the established echocardiographic parameters, allow a subclinical diagnosis of cardiac toxicity and a better stratification of the cancer patient, in addition to the identification of possible prevention and treatment routes in preclinical models. 

Epigenetic modulators in cardiovascular disease

MicroRNAs are small non-coding ribonucleic acid sequences (18-25nt) that play an essential role in gene expression at the post-transcriptional level. In recent years, the role of microRNAs in cardiovascular pathophysiology has attracted great interest. For this reason, in our group we have focused on studying its role in the pathophysiology of different cardiovascular diseases (heart failure, atrial fibrillation, amyloidosis, Brugada syndrome, etc.).

Miembros

Isabel Moscoso Galán
Postdoctoral researcher
imosgal@gmail.com
María Cebro Márquez
Posdoctoral researcher
mariacebrom@gmail.com
Ezequiel Álvarez Castro
Assistant professor
ezequiel.alvarez@usc.es
Ricardo Lage Fernández
Assistant professor
rlagef@gmail.com

 

Laura Vázquez Vázquez
PhD student
Nuria Chantada López
PhD student
Javier Martínez Fernández
Research collaborator
Simón Rodriguez Moar
Research collaborator
Marta Trillo Domínguez
Research Specialist Technician
Valentina Serrano Cruz
PhD student
Marta Esther Vilar Sánchez
PhD student
Iria Vidal Abeijón
Research Specialist Technician

Resultados seleccionados

Proposed mechanism of docetaxel induced cardiotoxicity: Involvement of ER stress. DTX induces BIP, CHOP, ATF6 expression and reduces GADD34 expression increasing phosphorylated eIF2a levels. Unresolved ER stress will eventually lead to cell death (caspase-mediated apoptosis). Rounded ends indicate inhibitory pathways; arrows indicate stimulatory pathways.

Spin-Offs

BFlow

B-Flow offers exclusive technology in a personalized way to build Organ-on-a-chip models which that reproduce the in vivo conditions.

FlowReverse

The innovative product is a digital report with personalized medicine indicators in cardiology to support diagnosis and treatment decision-making for patients with ischemic heart disease.

Alianzas

Centro de Investigación Biomédica en Red: Enfermedades Cardiovasculares