Esta web utiliza cookies para que podamos ofrecerte la mejor experiencia de usuario posible. La información de las cookies se almacena en tu navegador y realiza funciones tales como reconocerte cuando vuelves a nuestra web o ayudar a nuestro equipo a comprender qué secciones de la web encuentras más interesantes y útiles.

Investigadores
- Nuria Gago
- David Olmeda
Becarios Post-doctorales
- Susana Frago
- María Magdalena Leal
- Adriana Sanna
Becarios Pre-Doctorales
- Xavier Catena
- Marta Contreras
- Naiara Juan
- Sergio Oterino
- Javier Suárez
- Cristina Tejedo
Técnicos de Laboratorio
- Tonantzin Guadalupe Calvo
- Cynthia Mucientes
- Mireia Vallespinós
Melanomas are inherently aggressive cancers for which basic and translational research have significantly improved patient prognosis. Nevertheless, clinical responses are still incomplete. The long-term goals of our Group are to identify new progression biomarkers and therapeutic agents. We are particularly interested in mechanisms of cellular stress that, being selectively deregulated in melanoma, define lineage-specific vulnerabilities (publications in Nature, Cancer Cell, Nature Cell Biology, Nature Communications, among others). Our laboratory has also generated the firstin- class lymphoreporter mice for non-invasive imaging of pre-metastatic niches in melanoma (Nature). These systems have led to the validation of nanoparticle-based treatments that are currently being tested in clinical trials. Our ultimate objective is to improve the management of patients with otherwise refractory metastatic melanomas.
Publicaciones
- (2021). Melanoma models for the next generation of therapies. Cancer Cell (in press). Publicación CNIO.
- (2021). The State of Melanoma: Emergent Challenges and Opportunities. Clin Cancer Res (in press). Publicación CNIO.
- (2020). Lymph: (Fe)rrying Melanoma to Safety. Cancer Cell 38, 446-448. Publicación CNIO.
- (2020). Midkine rewires the melanoma microenvironment toward a tolerogenic and immune-resistant state. Nat Med 26, 1865-1877. Publicación CNIO.
- (2019). p62/SQSTM1 Fuels Melanoma Progression by Opposing mRNA Decay of a Selective Set of Pro-metastatic Factors. Cancer Cell 35, 46-63. Publicación CNIO.
- (2019). p62/SQSTM1 Fuels Melanoma Progression by Opposing mRNA Decay of a Selective Set of Pro-metastatic Factors.. Cancer Cell 35, 46-63. Publicación CNIO.
- (2019). KLF9-dependent ROS regulate melanoma progression in stage-specific manner. Oncogene 38, 3585-3597. Publicación CNIO.
- (2019). Antimetastatic dsRNA mimics identified by live imaging of pathogenic neolymphangiogenes. BioRivx (in press). Publicación CNIO.
- (2018). CD38 promotes pristane-induced chronic inflammation and increases susceptibility to experimental lupus by an apoptosis-driven and TRPM2-dependent mechanism. Sci Rep 8, 3357. Publicación CNIO.
Open Access
- (2017). Systems analysis identifies melanoma-enriched pro-oncogenic networks controlled by the RNA binding protein CELF1. Nat Commun 8, 2249. Publicación CNIO.
Open Access
- (2017). Whole-body imaging of lymphovascular niches identifies pre-metastatic roles of midkine.. Nature 546, 676-680. Publicación CNIO.
- (2017). Location, Location, Location: Spatio-Temporal Cues That Define the Cell of Origin in Melanoma. Cell Stem Cell 21, 559-561. Publicación CNIO.
- (2017). TYRP1 mRNA goes fishing for miRNAs in melanoma.. Nat Cell Biol 19, 1311-1312. Publicación CNIO.
- (2017). ATG5 mediates a positive feedback loop between Wnt signaling and autophagy in melanoma.. Cancer Res 77, 5873-5885. Publicación CNIO.
- (2017). DEK oncogene is overexpressed during melanoma progression.. Pigment Cell Melanoma Res 30, 194-202. Publicación CNIO.
- (2016). Lineage-specific roles of the cytoplasmic polyadenylation factor CPEB4 in the regulation of melanoma drivers. Nat Commun 7, 13418. Publicación CNIO.
Open Access
- (2016). UNR/CSDE1 Drives a Post-transcriptional Program to Promote Melanoma Invasion and Metastasis.. Cancer Cell 30, 694-707. Publicación CNIO.
- (2016). TRANSAUTOPHAGY: European network for multidisciplinary research and translation of autophagy knowledge.. Autophagy 12, 614-617. Publicación CNIO.
- (2016). The nuclear corepressor 1 and the thyroid hormone receptor ß suppress breast tumor lymphangiogenesis. Oncotarget 7, 78971-78984. Publicación CNIO.
- (2016). The state of melanoma: challenges and opportunities.. Pigment Cell Melanoma Res 29, 404-416. Publicación CNIO.
- (2016). Vesicular trafficking mechanisms in endothelial cells as modulators of the tumor vasculature and targets of antiangiogenic therapies.. FEBS J 283, 25-38. Publicación CNIO.
- (2016). Evaluation of the antiproliferative, proapoptotic, and antiangiogenic effects of a double-stranded RNA mimic complexed with polycations in an experimental mouse model of leiomyoma.. Fertil Steril 105, 529-538. Publicación CNIO.
- (2016). Understanding Tumor-Antigen Presentation in the New Era of Cancer Immunotherapy.. Curr Pharm Design 22, 6234-6250. Publicación CNIO.
- (2016). Metastatic risk and resistance to BRAF inhibitors in melanoma defined by selective allelic loss of ATG5.. Autophagy 12, 1776-1790. Publicación CNIO.