Role of Activator Protein-1 Complex on the Phenotype of Human Osteosarcomas Generated from Mesenchymal Stem Cells

Author:

Gambera Stefano1ORCID,Abarrategi Ander12ORCID,Rodríguez-Milla Miguel A.1,Mulero Francisca3,Menéndez Sofía T.45,Rodriguez René45ORCID,Navarro Samuel56,García-Castro Javier1ORCID

Affiliation:

1. Cellular Biotechnology Unit, Instituto de Salud Carlos III, Madrid, Spain

2. Haematopoietic Stem Cell Laboratory, The Francis Crick Institute, London, UK

3. Molecular Image Core Unit, Spanish National Cancer Research Centre, Madrid, Spain

4. Hospital Universitario Central de Asturias—Instituto de Investigación Sanitaria del Principado de Asturias and, Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain

5. CIBER de Cáncer (CIBERONC), Madrid, Spain

6. Pathology Department, University of Valencia, Valencia, Spain

Abstract

Abstract Osteosarcoma (OS) is a highly aggressive bone tumor that usually arises intramedullary at the extremities of long bones. Due to the fact that the peak of incidence is in the growth spurt of adolescence, the specific anatomical location, and the heterogeneity of cells, it is believed that osteosarcomagenesis is a process associated with bone development. Different studies in murine models showed that the tumor-initiating cell in OS could be an uncommitted mesenchymal stem cell (MSC) developing in a specific bone microenvironment. However, only a few studies have reported transgene-induced human MSCs transformation and mostly obtained undifferentiated sarcomas. In our study, we demonstrate that activator protein 1 family members induce osteosarcomagenesis in immortalized hMSC. c-JUN or c-JUN/c-FOS overexpression act as tumorigenic factors generating OS with fibroblastic or pleomorphic osteoblastic phenotypes, respectively.

Funder

Fondo de Investigaciones Sanitarias

Consorcio CIBERONC

Miguel Servet Program

Sara Borrell Program

Agencia Estatal de Investigación

Madrid Regional Government

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

Reference49 articles.

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