Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Concepcion Santiago-Fernandez.
Journal of Translational Medicine | 2015
Eduardo García-Fuentes; Concepcion Santiago-Fernandez; Carolina Gutierrez-Repiso; María Dolores Mayas; Wilfredo Oliva-Olivera; Leticia Coín-Aragüez; Juan Alcaide; Luis Ocaña-Wilhelmi; Joan Vendrell; Francisco J. Tinahones; Lourdes Garrido-Sánchez
BackgroundA key role for HIF-1α in the promotion and maintenance of dietary obesity has been proposed. We analyzed the association between hypoxia and de novo lipogenesis in human adipose tissue.MethodsWe studied HIF-1α mRNA and protein expression in fasting status in visceral adipose tissue (VAT) from non-obese and morbidly obese subjects, and in VAT from wild-type and ob/ob C57BL6J mice in both fasting and feeding status. We also analyzed the effect of hypoxia on the VAT mRNA expression of genes involved in lipogenesis.ResultsHIF-1α was increased in VAT from morbidly obese subjects. In fasting status, C57BL6J ob/ob mice had a higher VAT HIF-1α mRNA expression than C57BL6J wild-type mice. In feeding status, VAT HIF-1α mRNA expression significantly increased in C57BL6J wild-type, but not in C57BL6J ob/ob mice. In humans, HIF-1α mRNA expression correlated positively with body mass index and insulin resistance. VAT HIF-1α mRNA expression correlated negatively with ACC1, PDHB and SIRT3 mRNA expression, and positively with PPAR-γ. VAT explants incubated in hypoxia showed reduced SIRT3 and increased PPAR-γ, SREBP-1c, ACLY, ACC1 and FASN mRNA expression.ConclusionsMorbidly obese subjects have a higher level of VAT HIF-1α. Postprandial status is associated with an increase in HIF-1α mRNA expression in C57BL6J wild-type mice. Hypoxia alters the mRNA expression of genes involved in de novo lipogenesis in human VAT.
Surgery for Obesity and Related Diseases | 2016
Juan José González-Plaza; Carolina Gutierrez-Repiso; Sara García-Serrano; Francisca Rodriguez-Pacheco; Lourdes Garrido-Sánchez; Concepcion Santiago-Fernandez; Juan Garcia-Arnes; Francisco J. Moreno-Ruiz; Alberto Rodriguez-Cañete; Eduardo García-Fuentes
BACKGROUND The changes in the transcriptomic profiling of subcutaneous adipose tissue (SAT) when weight loss stabilizes after a Roux-en-Y gastric bypass (RYGB) are still largely unknown. OBJECTIVES To investigate the changes produced in SAT gene expression of morbidly obese women when their weight loss stabilizes 2 years after RYGB. SETTING University hospital. METHODS SAT biopsies of the periumbilical area were taken before and 2 years after RYGB. Gene expression levels were assessed by microarray analysis and significant differences in gene expression were validated by real-time quantitative polymerase chain reaction. The findings were also confirmed in an independent population of morbidly obese women. RESULTS Microarray analysis revealed that the overexpressed differentially expressed genes have a prominent role in the pathways involved in biosynthetic processes, especially lipid or carboxylic ones (stearoyl-Coenzyme A desaturase-1, fatty acid desaturase-1, fatty acid elongase-6, ATP citrate lyase, fatty acid synthase, lipin-1, monoacylglycerol O-acyltransferase, patatin-like phospholipase domain containing-3, phosphate cytidylyltransferase-2, cholesteryl ester transfer protein, transmembrane 7 superfamily member 2, pyruvate carboxylase, and glycogen synthase 2). Most of the underexpressed differentially expressed genes are related with immune system and inflammation processes (immune responses, response to stress, cell death, regulation of biological quality, immune effector process, the response to endogenous stimulus, and the response to other types of stimulus). CONCLUSION An improvement of the SAT inflammatory and immune profile and an induction of genes involved in the regulation of lipid metabolism are shown when weight loss stabilizes 2 years after RYGB. Most of the genes shown are clearly linked to obesity and other metabolic disorders.
International Journal of Medical Sciences | 2017
Luis M. Pérez-Belmonte; Inmaculada Moreno-Santos; Juan José Gómez-Doblas; José Manuel García-Pinilla; Luis Morcillo-Hidalgo; Lourdes Garrido-Sánchez; Concepcion Santiago-Fernandez; María G. Crespo-Leiro; Fernando Carrasco-Chinchilla; Pedro L. Sánchez-Fernández; Eduardo de Teresa-Galván; Manuel F. Jiménez-Navarro
Epicardial adipose tissue has been proposed to participate in the pathogenesis of heart failure. The aim of our study was to assess the expression of thermogenic genes (Uncoupling protein 1 (UCP1), peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α), and PR-domain-missing 16 (PRDM16) in epicardial adipose tissue in patients with heart failure, stablishing the difference according to left ventricular ejection fraction (reduced or preserved). Among the 75 patients in our study, 42.7% (n=32) had reduced left ventricular ejection fraction. UCP1, PGC1α and PRDM16 mRNA in EAT were significantly lower in patients with reduced left ventricular ejection fraction. Multiple regression analysis showed that age, male gender, body max index, presence of obesity, type-2-diabetes mellitus, hypertension and coronary artery disease and left ventricular ejection fraction were associated with the expression levels of UCP1, PGC1α and PRDM16 mRNA. Thermogenic genes expressions in epicardial adipose tissue (UCP1: OR 0.617, 95%CI 0.103-0.989, p=0.042; PGC1α: OR 0.416, 95%CI 0.171-0.912, p=0.031; PRDM16: OR 0.643, 95%CI 0.116-0.997, p=0.044) were showed as protective factors against the presence of heart failure with reduced left ventricular ejection fraction, and age (OR 1.643, 95%CI 1.001-3.143, p=0.026), presence of coronary artery disease (OR 6.743, 95%CI 1.932-15.301, p<0.001) and type-2-diabetes mellitus (OR 4.031, 95%CI 1.099-7.231, p<0.001) were associated as risk factors. The adequate expression of thermogenic genes has been shown as possible protective factors against heart failure with reduced ejection fraction, suggesting that a loss of functional epicardial adipose tissue brown-like features would participate in a deleterious manner on heart metabolism. Thermogenic genes could represent a future novel therapeutic target in heart failure.
Surgery for Obesity and Related Diseases | 2018
Juan José González-Plaza; Concepcion Santiago-Fernandez; Carolina Gutierrez-Repiso; Sara García-Serrano; Francisca Rodriguez-Pacheco; Ailec Ho-Plagaro; Lourdes Garrido-Sánchez; Francisco J. Moreno-Ruiz; Alberto Rodriguez-Cañete; Eduardo García-Fuentes
BACKGROUND The changes that are produced in the gene expression of subcutaneous adipose tissue after Roux-en-Y gastric bypass are not yet fully known. OBJECTIVE To identify the changes in the subcutaneous adipose tissue gene expression of morbidly obese women with low insulin resistance (MO-low-IR) and high insulin resistance (MO-high-IR) to find a relationship with measured obesity-related co-morbidities. SETTING A university hospital. METHODS Subcutaneous adipose tissue samples were assessed by microarray analysis before and 2 years after Roux-en-Y gastric bypass in MO-low-IR and MO-high-IR patients. RESULTS There is a group of shared differentially expressed genes (DEG) in both MO-low-IR and MO-high-IR, also there is a group of exclusive DEG in MO-low-IR and another group in MO-high-IR. In MO-high-IR, the downexpressed DEG are related to the regulation of transcription and are involved in the pathways related to cytokine-cytokine receptor interaction, cancer, phosphatidylinositol 3-kinase-protein kinase B signaling, human T-lymphotropic virus I infection, chemokine signaling, and Janus kinase/signal transducers and activators of transcription signaling. In MO-low-IR, the overexpressed DEG are related to carbohydrate metabolic processes, the downexpressed DEG to the glycosaminoglycan metabolic process and regulation of translation, and the pathways are related to phosphatidylinositol 3-kinase-protein kinase B signaling and metabolic pathways. The fold change of DEG mainly correlates with the percentage of change (Δ) of waist, Δhip, Δglucose, and Δtriglycerides. These DEG were mainly related to cancer, inflammation/immune regulation, metabolic pathways, ribonucleic acid/deoxyribonucleic acid regulation, virus infection, and regulation of cellular proliferation. CONCLUSIONS This study suggests a potential association between high insulin resistance and the expression of genes related to cancer and chronic immune activation/inflammation.
Endocrinología, Diabetes y Nutrición (English ed.) | 2017
Concepcion Santiago-Fernandez; Sara García-Serrano; Monica Tome; Sergio Valdés; Luis Ocaña-Wilhelmi; Alberto Rodriguez-Cañete; Francisco J. Tinahones; Eduardo García-Fuentes; Lourdes Garrido-Sánchez
Background and objective Ghrelin is a gastrointestinal peptide involved in regulation of body weight and energy balance. However, its behavior after bariatric surgery and its relationship to insulin resistance are still controversial. A simultaneous assessment was made of the association between changes in ghrelin levels and different variables after three types of bariatric surgery.
PLOS ONE | 2017
José Carlos Fernández-García; Juan Alcaide; Concepcion Santiago-Fernandez; Mm. Roca-Rodriguez; Zaida Agüera; Rosa M. Baños; Cristina Botella; Rafael de la Torre; José Manuel Fernández-Real; Gema Frühbeck; Javier Gómez-Ambrosi; Susana Jiménez-Murcia; José M. Menchón; Felipe F. Casanueva; Fernando Fernández-Aranda; Francisco J. Tinahones; Lourdes Garrido-Sánchez
PLOS ONE | 2017
José Carlos Fernández-García; Juan Alcaide; Concepcion Santiago-Fernandez; Mm. Roca-Rodriguez; Zaida Agüera; Rosa M. Baños; Cristina Botella; Rafael de la Torre; José Manuel Fernández-Real; Gema Frühbeck; Javier Gómez-Ambrosi; Susana Jiménez-Murcia; José M. Menchón; Felipe F. Casanueva; Fernando Fernández-Aranda; Francisco J. Tinahones; Lourdes Garrido-Sánchez
Obesity Surgery | 2018
S. Lopez; Sara García-Serrano; Carolina Gutierrez-Repiso; Francisca Rodriguez-Pacheco; Ailec Ho-Plagaro; Concepcion Santiago-Fernandez; Gonzalo Alba; Marta Cejudo-Guillén; Alberto Rodriguez-Cañete; Sergio Valdés; Lourdes Garrido-Sánchez; David Pozo; Eduardo García-Fuentes
Atherosclerosis | 2018
Ailec Ho-Plagaro; Carolina Gutierrez-Repiso; Sara García-Serrano; Concepcion Santiago-Fernandez; Lourdes Garrido-Sánchez; Miguel A. Alaminos-Castillo; Sergio Valdés; Montserrat Gonzalo; G. Alcain-martinez; A. rodriguez-moreno; Francisco J. Moreno-Ruiz; Custodia Montiel-Casado; Eduardo García-Fuentes
Atherosclerosis | 2017
Concepcion Santiago-Fernandez; Carolina Gutierrez-Repiso; José Manuel García-Almeida; Luis Ocaña-Wilhelmi; Jose Rivas-Becerra; Alejandro Rodriguez-Morata; Monica Tome; Wilfredo Oliva-Olivera; Eduardo García-Fuentes; Lourdes Garrido-Sánchez