Human osteosarcoma cells express functional receptor activator of nuclear factor-kappa B

• Published in: The Journal of pathology 2007-04, Vol.211 (5), p.555-562
• Main Authors: Mori, K, Le Goff, B, Berreur, M, Riet, A, Moreau, A, Blanchard, F, Chevalier, C, Guisle-Marsollier, I, Léger, J, Guicheux, J, Masson, M, Gouin, F, Rédini, F, Heymann, D
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Aged; Aged, 80 and over; Biological and medical sciences; Bone Neoplasms - chemistry; Cell Line, Tumor; Child; Cross-Sectional Studies; Diseases of the osteoarticular system; Female; Humans; Immunohistochemistry - methods; Investigative techniques, diagnostic techniques (general aspects); Male; Medical sciences; Middle Aged; Neoplasm Proteins - analysis; Osteoblasts - chemistry; osteoprotegerin; Osteoprotegerin - analysis; osteosarcoma; Osteosarcoma - chemistry; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Phosphorylation; RANK; RANK Ligand - metabolism; RANKL; Receptor Activator of Nuclear Factor-kappa B - analysis; Reverse Transcriptase Polymerase Chain Reaction - methods; RNA, Messenger - analysis; RNA, Neoplasm - analysis; signal transduction; Signal Transduction - physiology; Tumors of striated muscle and skeleton
• ISSN: 0022-3417; 1096-9896
• DOI: 10.1002/path.2140

RANK, RANK ligand (RANKL) and osteoprotegerin (OPG) are the key regulators of bone metabolism, both in normal and pathological conditions. Previous data have demonstrated that human osteosarcoma biopsies express RANKL as well as OPG, and functional RANK is expressed in a murine osteosarcoma cell line. As RANK expression in human osteosarcoma remains controversial, the aim of the present study was to analyse its expression in vitro in human osteosarcoma cell lines, ex vivo using pathological tissues, and then to determine its functionality in terms of signal transduction pathways modulated by RANKL. RT‐PCR analysis and immunohistochemistry experiments revealed that RANK is expressed at both transcriptional and protein levels in MNNG/HOS, Saos‐2 and MG‐63 human osteosarcoma cell lines, in contrast to the U‐2 OS osteosarcoma cell line and human osteoblasts, which were negative. RANK was also expressed in 57% of osteosarcoma biopsies. Furthermore, western blot experiments clearly demonstrated the functionality of RANK. Thus, RANKL significantly induced the phosphorylation of ERK1/2, p38 and IκB in RANK‐positive osteosarcoma cells. This study is the first report of functional RANK expression in human osteosarcoma cells: this strengthens the involvement of the RANK–RANKL–OPG axis in primary bone tumour biology and identifies novel therapeutic approaches targeting RANK‐positive osteosarcoma. Copyright © 2007 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.