RECK expression in osteosarcoma: correlation with matrix metalloproteinases activation and tumor invasiveness

J Orthop Res. 2007 May;25(5):696-702. doi: 10.1002/jor.20323.


Osteosarcoma is a malignant tumor of bone characterized by its high metastatic potential. For the development of metastasis, activation of matrix metalloproteinases (MMPs) is required. A novel MMPs inhibitor, reversion inducing cysteine rich protein with Kazal motifs (RECK), is known to down-regulate MMPs and suppress the invasive and metastatic potential in many tumor-derived cell lines and some types of tumors. The expression of RECK and its role in tumor invasiveness have never been studied in osteosarcoma. We examined RECK mRNA expression and MMPs activation in osteosarcoma using quantitative real time PCR, gelatin zymography, invasion assay, and transfection experiments. RECK was expressed but down-regulated in osteosarcoma cells. Activation of pro-MMP-2 was observed in all samples, whereas activation of MMP-2 and pro-MMP-9 was detected in only 11% and 7% of the samples, respectively. MMP-9 was not activated in any of the samples. The level of RECK expression was inversely correlated with pro-MMP-2 activation, and overexpression of RECK by transfection resulted in decreased pro-MMP-2 activation and reduced tumor invasiveness. These findings suggest that RECK plays an important role in the invasiveness of osteosarcoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Neoplasms / enzymology
  • Bone Neoplasms / pathology*
  • Enzyme Activation / physiology
  • GPI-Linked Proteins
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Matrix Metalloproteinase 2 / metabolism*
  • Matrix Metalloproteinase 9 / metabolism*
  • Membrane Glycoproteins / genetics*
  • Neoplasm Invasiveness
  • Osteosarcoma / enzymology
  • Osteosarcoma / pathology*
  • RNA, Messenger / metabolism
  • Transfection
  • Tumor Cells, Cultured


  • GPI-Linked Proteins
  • Membrane Glycoproteins
  • RECK protein, human
  • RNA, Messenger
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9