Arquitectura molecular en enfermedades autoinmunes tiroideas mediante transcriptómica espacial
PI22/01404
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Nombre agencia financiadora Instituto de Salud Carlos III
Acrónimo agencia financiadora ISCIII
Programa Programa Estatal para Impulsar la Investigación Científico-Técnica y su Transferencia
Subprograma Subprograma Estatal de Generación de Conocimiento
Convocatoria PI22- Proyectos de I+D+I en salud (AES 2022).
Año convocatoria 2022
Unidad de gestión Plan Estatal de Investigación Científica, Técnica y de Innovación 2021-2023
Centro beneficiario FUNDACION INVESTIGACION BIOMEDICA HOSPITAL DE LA PRINCESA
Centro realización INSTITUTO DE INVESTIGACION BIOMEDICA HOSPITAL UNIVERSITARIO DE LA PRINCESA
Identificador persistente http://dx.doi.org/10.13039/501100004587
Publicaciones
Resultados totales (Incluyendo duplicados): 1Encontrada(s) 1 página(s)
Primary Cilia as a Tumor Marker in Pituitary Neuroendocrine Tumors
Dipòsit Digital de Documents de la UAB
- Martínez-Hernández, Rebeca
- Serrano-Somavilla, Ana
- Fernández-Contreras, Raul
- Sanchez-Guerrero, Cristina
- Sánchez de la Blanca, Nuria
- Sacristán-Gómez, Pedro
- Sebastian-Valles, Fernando|||0000-0002-4127-0483
- Sampedro-Núñez, Miguel
- Fraga, Javier
- Calatayud, María|||0000-0002-6737-7289
- Vicente, Almudena
- García-de-Casasola, G|||0000-0002-5171-7373
- Sanz-García, Ancor
- Araujo-Castro, Marta|||0000-0002-0519-0072
- Ruz-Caracuel, Ignacio|||0000-0002-2298-4683
- Puig Domingo, Manuel|||0000-0002-6744-7195
- Marazuela, Mónica|||0000-0003-1158-9618
Pituitary neuroendocrine tumors (PitNETs) account for approximately 15% of all intracranial neoplasms. Although they usually appear to be benign, some tumors display worse behavior, displaying rapid growth, invasion, refractoriness to treatment, and recurrence. Increasing evidence supports the role of primary cilia (PC) in regulating cancer development. Here, we showed that PC are significantly increased in PitNETs and are associated with increased tumor invasion and recurrence. Serial electron micrographs of PITNETs demonstrated different ciliation phenotypes (dot-like versus normal-like cilia) that represented PC at different stages of ciliogenesis. Molecular findings demonstrated that 123 ciliary-associated genes (eg, doublecortin domain containing protein 2, Sintaxin-3, and centriolar coiled-coil protein 110) were dysregulated in PitNETs, representing the upregulation of markers at different stages of intracellular ciliogenesis. Our results demonstrate, for the first time, that ciliogenesis is increased in PitNETs, suggesting that this process might be used as a potential target for therapy in the future.