Vanesa García-Barberán

Dr. Vanesa García-Barberán

Molecular Oncology Laboratory, Medical Oncology Department, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 April 2014 in Genes, Chromosomes and Cancer
Verified
Journal Article
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MRMarta Rodríguez
Marta Rodríguez
JSJavier Silva
Javier Silva
ALAna López‐Alfonso
Ana López‐Alfonso
MLMaría Belen López‐Muñiz
María Belen López‐Muñiz
CPCristina Peña
Cristina Peña
FBFélix Bonilla
Félix Bonilla

29 April 2021 in Molecular Cancer
Verified
Journal Article
Open access
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MHMercedes Herrera
Mercedes Herrera
ABAlberto Berral-Gonzalez
Alberto Berral-Gonzalez
ICIgor Gregorio Lopez Cade
Igor Gregorio Lopez Cade
CGCristina Galindo-Pumariño
Cristina Galindo-Pumariño
SBSantiago Bueno-Fortes
Santiago Bueno-Fortes
Javier De Las RivasJavier De Las Rivas
Javier De Las Rivas

26 October 2015 in Oncotarget
Verified
Journal Article
Open access
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MRMarta Rodríguez
Marta Rodríguez
JSJavier Silva
Javier Silva
AHAlberto Herrera
Alberto Herrera
MHMercedes Herrera
Mercedes Herrera
CPCristina Peña
Cristina Peña
VGVanesa García-Barberán
Vanesa García-Barberán
Exosomes enriched in stemness/metastatic-related mRNAS promote oncogenic potential in breast cancer Exosomes enriched in stemness/metastatic-related mRNAS promote oncogenic potential in breast cancer

22 March 2017 in BMC Cancer
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Journal Article
Open access
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JGJosé Ángel García-Saénz
José Ángel García-Saénz
PAPatricia Ayllón
Patricia Ayllón
MLMarion Laig
Marion Laig
DADaniel Acosta-Eyzaguirre
Daniel Acosta-Eyzaguirre
MGMarta García-Esquinas
Marta García-Esquinas
ARAtocha Romero
Atocha Romero
Accurate measurement of tumor burden in breast cancer disease is essential to improve the clinical management of patients. In this study, we evaluate whether the fluctuations in the fraction of PIK3CA mutant allele correlates with tumor response according to RECIST criteria and tumor markers quantification. Eighty six plasma samples were analyzed by digital PCR using Rare Mutation Assays for E542K, E545K and H1047R. Mutant cfDNA and tumor markers CA15-3 and CEA were compared with radiographic imaging. The agreement between PIK3CA mutation status in FFPE samples and circulating tumor DNA (ctDNA) was moderate (K = 0.591; 95% IC = 0.371–0.811). Restricting the analysis to the metastatic patients, we found a good agreement between PIK3CA mutation status assessed in liquid and solid biopsy (K = 0.798 95%; IC = 0.586–1). ctDNA showed serial changes with fluctuations correlating with tumor markers 15.3 and CEA in 7 out of 8 cases with Pearson correlation coefficients ranging from 0.99 to 0.46 and from 0.99 to 0.38 respectively. Similarly, fluctuations in the fraction of PIK3CA mutant allele always correlated with changes in lesion size seen on images, although in two cases it did not correlate with treatment responses as defined by RECIST criteria. oncogenic mutation quantification in plasma samples can be useful to monitor treatment outcome. However, it might be limited by tumor heterogeneity in advanced disease and it should be evaluated together with radiographic imaging.

3 August 2018 in Molecular Cancer
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Journal Article
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MHMercedes Herrera
Mercedes Herrera
CLCarlos Llorens
Carlos Llorens
SRSocorro María Rodríguez-Pinilla
Socorro María Rodríguez-Pinilla
AHAlberto Herrera
Alberto Herrera
RRRicardo Ramos-ruiz
Ricardo Ramos-ruiz
Cristina PeñaCristina Peña
Cristina Peña
Exosome production from cancer-associated fibroblasts seems to be an important driver of tumor progression. We report the first in-depth biotype characterization of ncRNAs, analyzed by Next Generation Sequencing and Bioinformatics, expressed in established primary human normal and cancer-associated fibroblasts (CAFs) from cancer and normal mucosa tissues from 9 colorectal cancer patients, and/or packaged in their derived exosomes. Differential representation and enrichment analyses based on these ncRNAs revealed a significant number of differences between the ncRNA content of exosomes and the expression patterns of the normal and cancer-associated fibroblast cells. ncRNA regulatory elements are specifically packaged in CAF-derived exosomes, supporting a specific cross-talk between CAFs and colon cancer cells and/or other stromal cells, mediated by exosomes. These sncRNAs are potential biomarkers present in cancer-associated fibroblast-derived exosomes, which should thereby contribute to developing new non-invasive diagnostic, prognostic and predictive methods for clinical applications in management of cancer patients.

22 March 2017 in Oncotarget
Verified
Journal Article
Open access
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Mariano ProvencioMariano Provencio
Mariano Provencio
MRMarta Rodríguez
Marta Rodríguez
BCBlanca Cantos
Blanca Cantos
PSPilar Sabín
Pilar Sabín
CQCristina Quero
Cristina Quero
VGVanesa García-Barberán
Vanesa García-Barberán
MRNA in exosomas as a liquid biopsy in non-Hodgkin Lymphoma: a multicentric study by the Spanish Lymphoma Oncology Group mRNA in exosomas as a liquid biopsy in non-Hodgkin Lymphoma: a multicentric study by the Spanish Lymphoma Oncology Group