Bone Environment is Essential for Osteosarcoma Development from Transformed Mesenchymal Stem Cells. (17th April 2014)

• Record Type: Journal Article
• Authors: Rubio, Ruth; Abarrategi, Ander; Garcia‐Castro, Javier; Martinez‐Cruzado, Lucia; Suarez, Carlos; Tornin, Juan; Santos, Laura; Astudillo, Aurora; Colmenero, Isabel; Mulero, Francisca; Rosu‐Myles, Michael; Menendez, Pablo; Rodriguez, Rene
• Is Part Of: Stem cells. Volume 32:Number 5(2014:May)
• Page Start: 1136
• Page End: 1148
• Publication Date: 2014-04-17
• Subjects: Mesenchymal stem cells -- Osteosarcoma -- Bone -- Tumoral microenvironment -- p53 -- Rb -- Bone morphogenetic protein‐2 -- WNT signaling; Cloning -- Periodicals; Clone cells -- Periodicals; Stem cells -- Periodicals; Cell Differentiation -- Periodicals; Cell Division -- Periodicals; Clone Cells -- Periodicals; Hematopoietic Stem Cells -- Periodicals; Stem Cells -- Periodicals; 571.84
• DOI: 10.1002/stem.1647
• Languages: English
• ISSNs: 1066-5099

Abstract

Abstract: The cellular microenvironment plays a relevant role in cancer development. We have reported that mesenchymal stromal/stem cells (MSCs) deficient for p53 alone or together with RB (p53 −/− RB −/− ) originate leiomyosarcoma after subcutaneous (s.c.) inoculation. Here, we show that intrabone or periosteal inoculation of p53 −/− or p53 −/− RB −/− bone marrow‐ or adipose tissue‐derived MSCs originated metastatic osteoblastic osteosarcoma (OS). To assess the contribution of bone environment factors to OS development, we analyzed the effect of the osteoinductive factor bone morphogenetic protein‐2 (BMP‐2) and calcified substrates on p53 −/− RB −/− MSCs. We show that BMP‐2 upregulates the expression of osteogenic markers in a WNT signaling‐dependent manner. In addition, the s.c. coinfusion of p53 −/− RB −/− MSCs together with BMP‐2 resulted in appearance of tumoral osteoid areas. Likewise, when p53 −/− RB −/− MSCs were inoculated embedded in a calcified ceramic scaffold composed of hydroxyapatite and tricalciumphosphate (HA/TCP), tumoral bone formation was observed in the surroundings of the HA/TCP scaffold. Moreover, the addition of BMP‐2 to the ceramic/MSC implants further increased the tumoral osteoid matrix. Together, these data indicate that bone microenvironment signals are essential to drive OS development. Stem Cells 2014;32:1136–1148