| Literature DB >> 24979572 |
Daniela Piazzolla1, Adelaida R Palla2, Cristina Pantoja2, Marta Cañamero3, Ignacio Perez de Castro4, Sagrario Ortega5, Gonzalo Gómez-López6, Orlando Dominguez7, Diego Megías8, Giovanna Roncador9, Jose L Luque-Garcia10, Beatriz Fernandez-Tresguerres11, Agustin F Fernandez12, Mario F Fraga13, Manuel Rodriguez-Justo14, Miguel Manzanares11, Marta Sánchez-Carbayo15, Juana María García-Pedrero16, Juan P Rodrigo16, Marcos Malumbres4, Manuel Serrano1.
Abstract
NANOG is a pluripotency transcription factor in embryonic stem cells; however, its role in adult tissues remains largely unexplored. Here we show that mouse NANOG is selectively expressed in stratified epithelia, most notably in the oesophagus where the Nanog promoter is hypomethylated. Interestingly, inducible ubiquitous overexpression of NANOG in mice causes hyperplasia selectively in the oesophagus, in association with increased cell proliferation. NANOG transcriptionally activates the mitotic programme, including Aurora A kinase (Aurka), in stratified epithelia, and endogenous NANOG directly binds to the Aurka promoter in primary keratinocytes. Interestingly, overexpression of Nanog or Aurka in mice increased proliferation and aneuploidy in the oesophageal basal epithelium. Finally, inactivation of NANOG in cell lines from oesophageal or head and neck squamous cell carcinomas (ESCCs or HNSCCs, respectively) results in lower levels of AURKA and decreased proliferation, and NANOG and AURKA expression are positively correlated in HNSCCs. Together, these results indicate that NANOG has a lineage-restricted mitogenic function in stratified epithelia.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24979572 DOI: 10.1038/ncomms5226
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919