Knockdown of S100A4 Decreases Tumorigenesis and Metastasis in Osteosarcoma Cells by Repression of Matrix Metalloproteinase-9

Zhang, Guoyou;Li, Ming;Jin, Jing;Bai, Yushu;Yang, Changwei

  • Published : 20110800

Abstract

Osteosarcoma (OS), the most frequent bone tumor in children and adolescents, is highly malignant. Metastases are the major cause of death, and patients with relapse have a poor prognosis. Given the associations of S100A4 with OS and tumor metastasis, we explored its potential roles in OS metastasis. Among 32 OS (16 metastatic and 16 non-metastatic) specimens examined, we found a significant increase of S100A4 mRNA in metastatic tissues, and more importantly, expression of S100A4 and MMP-9 to be strongly correlated in patients who had lymph node or distant metastasis. We observed that siRNA mediated suppression of the S100A4 gene significantly reduced the proliferative and invasive capability of highly invasive OS cells, with a reduced rate of tumor growth and metastasis under in vivo conditions. Matrix metalloproteinase 9 (MMP-9) proved highly responsive to S100A4 gene suppression, demonstrating significant reduction in proteolytic activity, while overexpression of S100A4 increased the expression and proteolytic activity of MMP-9. Links of S100A4 with cell motility were confirmed by depletion which resulted in reduced cell migration. Moreover, loss of cell metastatic potential was completely rescued by overexpression of MMP-9. Collectively, our findings indicate that S100A4 contributes to OS metastasis by stimulating MMP-9 expression, suggesting potential as a novel diagnostic biomarker for OS progression as well as a therapeutic target.

Keywords

References

  1. Bjornland K, Flatmark K, Pettersen S, et al (2005). Matrix metalloproteinases participate in osteosarcoma invasion. J Surg Res, 127, 151-6. https://doi.org/10.1016/j.jss.2004.12.016
  2. Berge G, Pettersen S, Grotterød I, et al (2010). Osteopontin-An important downstream effector of S100A4-mediated invasion and metastasis. Int J Cancer, 18, 240-6.
  3. Bakhshi S, Radhakrishnan V (2010). Prognostic markers in osteosarcoma. Expert Rev Anticancer Ther, 10, 271-87. https://doi.org/10.1586/era.09.186
  4. Chen NH, Liu JW, Zhong JJ (2008). Ganoderic acid Me inhibits tumor invasion through down-regulating matrix metalloproteinases 2/9 gene expression. J Pharmacol Sci, 108, 212-6. https://doi.org/10.1254/jphs.SC0080019
  5. Cho HJ, Lee TS, Park JB, et al (2007).Disulfiram suppresses invasive ability of osteosarcoma cells via the inhibition of MMP-2 and MMP-9 expression. J Biochem Mol Biol, 40, 1069-76. https://doi.org/10.5483/BMBRep.2007.40.6.1069
  6. Ferrari C, Benassi S, Ponticelli F, et al (2004). Role of MMP-9 and its tissue inhibitor TIMP-1 in human osteosarcoma: findings in 42 patients followed for 1-16 years. Acta Orthop Scand, 75, 487-91. https://doi.org/10.1080/00016470410001295-1
  7. Himelstein BP, Asada N, Carlton MR, et al (1998).Matrix metalloproteinase-9 (MMP-9) expression in childhood osseous osteosarcoma. Med Pediatr Oncol, 31, 471-4. https://doi.org/10.1002/(SICI)1096-911X(199812)31:6<471::AID-MPO2>3.0.CO;2-M
  8. Huang LY, Xu Y, Cai GX, et al (2011). S100A4 over-expression underlies lymph node metastasis and poor prognosis in colorectal cancer. World J Gastroenterol, 17, 69-78. https://doi.org/10.3748/wjg.v17.i1.69
  9. Hoon DS, Ferris R, Tanaka R, et al (2011). Molecular mechanisms of metastasis. J Surg Oncol, 103, 508-17. https://doi.org/10.1002/jso.21690
  10. Ismail NI, Kaur G, Hashim H, et al (2008). S100A4 overexpression proves to be independent marker for breast cancer progression. Cancer Cell Int, 8, 12. https://doi.org/10.1186/1475-2867-8-12
  11. Kido A, Tsutsumi M, Iki K, et al (1999).Overexpression of matrix metalloproteinase (MMP)-9 correlates with metastatic potency of spontaneous and 4-hydroxyaminoquinoline 1-oxide (4-HAQO)-induced transplantable osteosarcomas in rats. Cancer Lett, 137, 209-16. https://doi.org/10.1016/S0304-3835(98)00368-1
  12. Kushlinsky NE, Solovyov YN, Babkina IV, et al (2010).Matrix metalloproteinases 2, 7, 9 and tissue inhibitor of matrix metalloproteinase-1 in the sera of patients with bone tumors. Bull Exp Biol Med, 149, 233-5. https://doi.org/10.1007/s10517-010-0914-3
  13. Lo JF, Yu CC, Chiou SH, et al (2011). The epithelial-mesenchymal transition mediator S100A4 maintains cancer-initiating cells in head and neck cancers. Cancer Res, 71, 1912-23. https://doi.org/10.1158/0008-5472.CAN-10-2350
  14. Mencia N, Selga E, Rico I, et al (2010). Overexpression of S100A4 in human cancer cell lines resistant to methotrexate.BMC Cancer, 10, 250-6. https://doi.org/10.1186/1471-2407-10-250
  15. Ma X, Yang Y, Wang Y, et al (2010). Small interfering RNA-directed knockdown of S100A4 decreases proliferation and invasiveness of osteosarcoma cells. Cancer Lett, 299, 171-81. https://doi.org/10.1016/j.canlet.2010.08.016
  16. Matsuyama Y, Takao S, Aikou T (2002). Comparison of matrix metalloproteinase expression between primary tumors with or without liver metastasis in pancreatic and colorectal carcinomas. J Surg Oncol, 80, 105-10. https://doi.org/10.1002/jso.10106
  17. Tarabykina S, Griffiths TR, Tulchinsky E, et al (2007). Metastasis-associated protein S100A4: spotlight on its role in cell migration. Curr Cancer Drug Targets, 7, 217-28. https://doi.org/10.2174/156800907780618329
  18. Yang X, Staren ED, Howard JM, et al (2001). Invasiveness and MMP expression in pancreatic carcinoma. Surg Res, 98, 33-9. https://doi.org/10.1006/jsre.2001.6150