Elena García

ORCID: 0000-0003-2638-2425
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About
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Research Areas
  • Cancer Treatment and Pharmacology
  • HIV/AIDS Research and Interventions
  • HIV/AIDS drug development and treatment
  • Colorectal Cancer Treatments and Studies
  • Pancreatic and Hepatic Oncology Research
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Cancer Cells and Metastasis
  • HIV Research and Treatment
  • Lung Cancer Treatments and Mutations
  • Cancer, Hypoxia, and Metabolism
  • Circadian rhythm and melatonin
  • Ubiquitin and proteasome pathways
  • Pregnancy and Medication Impact
  • Monoclonal and Polyclonal Antibodies Research
  • DNA Repair Mechanisms
  • Cancer, Lipids, and Metabolism
  • HER2/EGFR in Cancer Research
  • Social Sciences and Policies
  • Chronic Lymphocytic Leukemia Research
  • Genetics, Aging, and Longevity in Model Organisms
  • Telomeres, Telomerase, and Senescence
  • Ferroptosis and cancer prognosis
  • Cancer Genomics and Diagnostics
  • Hedgehog Signaling Pathway Studies
  • Peptidase Inhibition and Analysis

Spanish National Cancer Research Centre
2011-2024

Universidad Europea
2020-2022

Hospital Universitario Infanta Sofía
2022

Instituto de Salud Carlos III
2011-2022

Centro de Investigación Biomédica en Red
2022

Hospital Universitario Fundación Alcorcón
2014-2015

Centro de Investigación del Cáncer
2013

Azienda Ospedaliera Universitaria Pisana
2012

Centro Nacional de Investigaciones Científicas
2012

Institute of Oncology Ljubljana
2012

<h3>Objectives</h3> The tumour stroma/microenvironment not only provides structural support for development, but more importantly it cues to cancer stem cells (CSCs) that regulate their self-renewal and metastatic potential. This is certainly true pancreatic ductal adenocarcinomas (PDAC), where tumour-associated fibroblasts, stellate immune create an abundant paracrine niche CSCs via microenvironment-secreted factors. Thus understanding the role stroma play in PDAC development CSC biology of...

10.1136/gutjnl-2014-308935 article EN Gut 2015-04-03

Abstract The mechanistic target of rapamycin complex 1 controls cellular anabolism in response to growth factor signaling and nutrient sufficiency signaled through the Rag GTPases. Inhibition mTOR reproducibly extends longevity across eukaryotes. Here we report that mice endogenously express active mutant variants RagC exhibit multiple features parenchymal damage include senescence, expression inflammatory molecules, increased myeloid inflammation with extensive inflammaging a ~30% reduction...

10.1038/s43587-024-00635-x article EN cc-by Nature Aging 2024-06-07

Human epidermal growth factor receptor 2 (HER2) amplification is frequent in ductal carcinoma situ (DCIS) of the breast and associated with poorly differentiated tumors adverse prognosis features. This study aimed to determine molecular effects HER2 inhibitor lapatinib patients positive DCIS. Patients DCIS received 1,500 mg daily for four consecutive weeks prior surgical resection. Magnetic resonance imaging (MRI) was used changes tumor volume. The on signaling (PI3K/AKT RAS/MAPK pathways),...

10.1186/bcr3695 article EN cc-by Breast Cancer Research 2014-08-01
Marta Ruiz‐Algueró Belén Alejos Cristina García Yubero Melchor Riera Jaume José Antonio Iribarren and 95 more Víctor Asensi Francisco Pasquau Carlos Galera Mario Carrasco Adolfo Muñoz Carrero Inmaculada Jarrín Inés Suárez‐García Santiago Moreno Inmaculada Jarrín David Dalmau María Luisa Navarro Maria Gonzalez José Luís Blanco Féderico García Rafael Rubio José Antonio Iribarren Félix Gutiérrez Francesc Vidal Juan Berenguer Juan González Belén Alejos Víctoria Hernando Cristina Moreno Carlos Iniesta Luis Miguel Garcia Sousa Nieves Sanz Perez María Ángeles Muñoz‐Fernández Isabel García-Merino Irene Consuegra Fernández Coral Gómez Rico Jorge Gallego de la Fuente Paula Palau Concejo Joaquín Portilla Esperanza Merino Sergio Reus Vicente Boix Livia Giner Carmen Gadea Irene Portilla M. Pampliega Marcos Díez Juan Carlos Rodrı́guez José Sánchez‐Payá Juan Luís Gómez Jehovana Hernández María Remedios Alemán Valls María del Mar Alonso María Inmaculada Hernández Felícitas Díaz-Flores Dácil García Ricardo Pelazas Ana López Lirola José Sanz Moreno Alberto Arranz Caso Cristina Hernández Gutiérrez María Novella Mena Rafael Rubio Federico Pulido Otilia Bisbal Asunción Hernando Lourdes Domínguez David Rial‐Crestelo Laura Muñoz Bermejo Mireia Santacreu José Antonio Iribarren Julio Arrizabalaga María José Aramburu Xabier Camino Francisco Rodríguez-Arrondo Miguel Ángel von Wichmann Lidia Pascual Tomé Miguel Ángel Goenaga Ma Jesús Bustinduy Harkaitz Azkune Maialen Ibarguren Aitziber Lizardi Xabier Kortajarena Félix Gutiérrez Mar Masiá Sergio Padilla Andrés Navarro‐Ruiz Fernando Montolio Catalina Robledano Joan Gregori Colomé Araceli Adsuar Rafael J. Pascual Marta Fernández‐González Elena García José Alberto García Xavier Barber Roberto Muga Arantza Sanvisens Daniel Fuster Juan Berenguer Juan Carlos López Bernaldo de Quirós

The present study sought to describe the use of generic drugs and single-tablet regimen (STR) de-simplification for treatment human immunodeficiency virus (HIV) infection among 41 hospitals from cohort Spanish HIV/AIDS Research Network (CoRIS). In June 2018, we collected information on when antiretroviral (ARVs) were introduced in different hospitals, how decisions them made, was provided patients. Most nine available ARVs Spain by 2018 had been at least 85% participating except zidovudine...

10.1089/aid.2021.0122 article EN AIDS Research and Human Retroviruses 2022-03-31
Inés Suárez‐García Cristina Moreno Marta Ruiz‐Algueró Marı́a Jesús Pérez-Elı́as Marta Navarro and 95 more Marcos Díez Martínez Pompeyo Viciana Laura Pérez‐Martínez Miguel Górgolas Concha Amador Miguel Alberto de Zárraga Inmaculada Jarrín Santiago Moreno Inmaculada Jarrín David Dalmau Marı́a Luisa Navarro María Isabel González Féderico García Eva Poveda José Antonio Iribarren Félix Gutiérrez Rafael Rubio Francesc Vidal Juan Berenguer Juan González María Ángeles Muñoz‐Fernández Inmaculada Jarrín Belén Alejos Cristina Moreno Carlos Iniesta Luis Miguel Garcia Sousa Nieves Sanz Perez Marta Rava María Ángeles Muñoz‐Fernández Irene Consuegra Fernández Esperanza Merino Gema García Irene Portilla Iván Agea Joaquín Portilla José Sánchez‐Payá Juan Carlos Rodrı́guez L. Gimeno Livia Giner Marcos Díez Melissa Carreres Sergio Reus Vicente Boix Diego Torrús Ana López Lirola Dácil García Felícitas Díaz-Flores Juan Luís Gómez María del Mar Alonso Ricardo Pelazas Jehovana Hernández María Remedios Alemán Valls María Inmaculada Hernández Víctor Asensi Eulalia Valle-Garay María Eugenia Rivas Carmenado Tomás Suárez-Zarracina Secades Laura Pérez‐Martínez Rafael Rubio Federico Pulido Otilia Bisbal Asunción Hernando Lourdes Domínguez David Rial‐Crestelo Laura Muñoz Bermejo Mireia Santacreu José Antonio Iribarren Julio Arrizabalaga María José Aramburu Xabier Camino Francisco Rodríguez-Arrondo Miguel Ángel von Wichmann Lidia Pascual Tomé Miguel Ángel Goenaga Ma Jesús Bustinduy Harkaitz Azkune Maialen Ibarguren Aitziber Lizardi Xabier Kortajarena Ma Pilar Carmona Oyaga Maitane Umérez Igartua Félix Gutiérrez Mar Masiá Sergio Padilla Andrés Navarro‐Ruiz Fernando Montolio Catalina Robledano Joan Gregori Colomé Araceli Adsuar Rafael J. Pascual Marta Fernández Elena García José Alberto García Xavier Barber Roberto Muga

Abstract Background The aim of this study was to investigate the effectiveness and tolerability combination elvitegravir/cobicistat/tenofovir/emtricitabine plus darunavir (EVG/COB/TFV/FTC + DRV) in treatment-experienced patients from cohort Spanish HIV/AIDS Research Network (CoRIS). Methods Treatment-experienced starting treatment with EVG/COB/TFV/FTC DRV during years 2014–2018 more than 24 weeks follow-up were included. TFV could be administered either as tenofovir disoproxil fumarate or...

10.1186/s12981-020-00302-2 article EN cc-by AIDS Research and Therapy 2020-07-20

3543 Background: Chemotherapy (Ch) options for patients (pts) with colorectal cancer (CRC) have increased in the last years. However, there are no validated prospective molecular markers CRC to select which agents better treat any individual case. The aim of this study was determine efficacy terms progression free survival (PFS) a biomarker panel guide treatment selection setting. Methods: Treatment naive, ECOG 0-1, metastatic pts were accrued. Pts prospectively analyzed predefined set 10...

10.1200/jco.2013.31.15_suppl.3543 article EN Journal of Clinical Oncology 2013-05-20

11033 Background: FVB MMTV PyMT is a great mouse model for studying LBC due to its stochastic nature, immune system preservation, natural growth kinetics and ER/HER2 status. We approached the transcriptomic (T), proteomic (P), phospho-proteomic (P-P) metabonomic (M) layers of regulation tumor phenotype attempting unravel mechanisms resistance antiangiogenic drugs (ADs) find new targets. Methods: Treatments started when tumors measured 0,1cm 3 ; with VEGFR/PDGFR inhibitor BIBF 85mg/kg/day;...

10.1200/jco.2013.31.15_suppl.11033 article EN Journal of Clinical Oncology 2013-05-20
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