Scientific Program
Physiological and pathological processes
RESEARCH GROUP
Mitochondrial dysfunction in metabolic diseases

Eduardo Balsa Martinez
The Balsa laboratory seeks to understand the basic molecular components that regulate cellular metabolism and integrate this knowledge in the context of human physiology and disease. We focus on two central areas; First, we aim to elucidate the molecular mechanisms whereby mitochondrial dysfunction compromises cellular and organ fitness. Second, we focus on understanding the nutrient and metabolic dependencies of metastasizing cancer cells.

Research
Mitochondria are unique and complex organelles that perform essential functions in many aspects of cell biology. Once considered to be mere sites of ATP generation, it is now evident that these organelles participate in a wide range of cellular processes including calcium homeostasis, apoptosis, redox balance or cell fate. Because of this multifaceted contribution of mitochondria to key biologic and metabolic pathways it is not surprising that mitochondrial dysfunction has been linked to many human disorders including neurodegeneration, diabetes, cancer or aging. The Balsa laboratory seeks to understand the basic molecular components that regulate mitochondrial function and integrate this knowledge in the context of human physiology and disease.
We are currently exploring two central areas. First, we aim to elucidate the molecular mechanisms whereby mitochondrial dysfunction compromise cellular fitness and leads to organ failure in the context of human diseases. Second, we focus on understanding how cancer cells adapt to unfavoured tumour microenvironments by rewiring their mitochondrial metabolism to enable tumour growth and survival.
Group members

Sara Laine Menéndez
Lab.: 427 Ext.: 4740
sara.laine(at)cbm.csic.es

Eduardo Balsa Martínez
Lab.: 427 Ext.: 4739
ebalsa(at)cbm.csic.es

Lucía del Prado Montero
Lab.: 427 Ext.: 4740
ldelprado(at)cbm.csic.es

Alba Roca Portoles
Lab.: 427 Ext.: 4740
alba.roca(at)cbm.csic.es

Marcos Javier Zamora Dorta
Lab.: 427 Ext.: 4740
mzamora(at)cbm.csic.es

Raquel Losada de Paz
Lab.: 427 Ext.: 4740
rlosada(at)cbm.csic.es

Pablo Castillo Serrulla
Lab.: 427 Ext.: 4740
pcastillo(at)cbm.csic.es

Miriam Jaraíz Rodríguez
Lab.: 427 Ext.: 4739
mjaraiz(at)cbm.csic.es

Víctor Manuel Cruz Vilchez
Lab.: 427 Ext.: 4739
vmcruz(at)cbm.csic.es

Natalia del Pozo Ramos
Lab.: 427 Ext.: 4740
ndelpozo(at)cbm.csic.es

Sophie Coahen
Lab.: 427 Ext.: 4740

Natalia Brun Rubio
Lab.: 427 Ext.: 4740

Daniel Curbelo Piñero
Lab.: 427 Ext.: 4739
daniel.curbelo(at)cbm.csic.es
Selected publications
Metabolic remodeling in astrocytes: Paving the path to brain tumor development
Myriam Jaraíz-Rodríguez et al.
Defective NADPH production in mitochondrial disease complex I causes inflammation and cell death
Eduardo Balsa et al.
ER and Nutrient Stress Promote Assembly of Respiratory Chain Supercomplexes through the PERK-eIF2α Axis
Eduardo Balsa et al.
Bromodomain Inhibitors Correct Bioenergetic Deficiency Caused by Mitochondrial Disease Complex I Mutations
Joeva J Barrow et al.