Developmental and Oncogenic Signaling
The team's goal is to study the molecular mechanisms that take place during embryonic development to form a complete and functional organism and how these mechanisms are affected in pathological situations such as cancer. We believe that if we know these mechanisms we will better understand how our organism functions and, moreover, we hope that this knowledge will lay the foundations for the design of new therapeutic approaches in different diseases.
We use genetically modified mice as an animal model for our studies. The advantage of this model is that it is a vertebrate with a physiology very similar to ours. The possibility of making genetic modifications allows us to evaluate the relevance, in vivo, of the molecular mechanisms that we study in development and to create animal models of pathological situations that allow us to better understand the disease and thus propose new therapeutic approaches. In our studies, we use different techniques that cover various levels of experimentation: from animal behaviour and the analysis of different tissues of these genetically modified mice using specialised microscopy to primary cell cultures, biochemical and molecular assays that include cutting-edge techniques in gene manipulation such as CRISPR/Cas technology.
In our research we have defined three study models: the embryonic development of the genitourinary system (coordinated by Dr. Encinas), the embryonic development of the nervous system (coordinated by Dr. Egea) and the generation of mouse models of endometrial carcinogenesis (coordinated by Dr. Dolcet). In this way we aim to have a broader and more integrative view of the molecular mechanisms involved in embryonic development and which, if affected, can give rise to diseases such as cancer.
Featured publications
Roy R; Lorca C; Mulet M; Sánchez Milán JA; Baratas A; de la Casa M; Espinet C; Serra A; Gallart-Palau X
Altered ureido protein modification profiles in seminal plasma extracellular vesicles of non-normozoospermic men.
Frontiers in Endocrinology 14 1113824-1113824. .
Altes, G; Vaquero, M; Cuesta, S; Anerillas, C; Macia, A; Espinet, C; Ribera, J; Bellusci, S; Klein, OD; Yeramian, A; Dolcet, X; Egea, J; Encinas, M
A dominant negative mutation uncovers cooperative control of caudal Wolffian duct development by Sprouty genes
Cellular And Molecular Life Sciences 79 514-514. .
Diéguez-Martínez N; Espinosa-Gil S; Yoldi G; Megías-Roda E; Bolinaga-Ayala I; Viñas-Casas M; Gorgisen G; Domingo-Ortí I; Pérez-Montoyo H; Bayascas JR; Colas E; Dolcet X; Lizcano JM
The ERK5/NF-?B signaling pathway targets endometrial cancer proliferation and survival.
Cellular And Molecular Life Sciences 79 524-524. .
Responsable/s de grup
Mario Encinas Martin
Francisco Javier Dolcet Roca
Biomedicine I / Biomedicina I
1st – 2nd floor / 1a – 2a planta