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.

Latest publications

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