Expression of vascular endothelial growth factor and matrix metalloproteinase-9 in sacral chordoma

被引:0
作者
Kang-Wu Chen
Hui-Lin Yang
Jian Lu
Gen-Lin Wang
Yi-Ming Ji
Gui-Zhong Wu
Li-Fan Zhu
Jia-Yong Liu
Xiao-Qing Chen
Yong-Ping Gu
机构
[1] The First Affiliated Hospital of Soochow University,Department of Orthopedic Surgery
[2] University of Toledo Medical Center,Department of Orthopedic Surgery
[3] Affiliated Hospital of Nantong University,Department of Orthopedic Surgery
[4] The First Affiliated Hospital of Soochow University,Department of Pathology
来源
Journal of Neuro-Oncology | 2011年 / 101卷
关键词
Chordoma; Sacrum; Vascular endothelial growth factor; Matrix metalloproteinase-9;
D O I
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中图分类号
学科分类号
摘要
Sacral chordoma is a vessel-rich and infiltrative tumor, but the fundamental knowledge of its biological behavior remains unknown. This study was designed to investigate the expression levels and contributions of vascular endothelial growth factor (VEGF) and matrix metalloproteinase-9 (MMP-9) in the angiogenesis and recurrence of sacral chordoma and their correlations. An immunohistochemical method was used to investigate the expression of VEGF, MMP-9, and microvascular density (MVD) in 36 patients with sacral chordoma. Their differences in expressions were statistically analyzed and their correlations with angiogenesis and recurrence were evaluated. The mean MVD of sacral chordomas was significantly higher than that of the adjacent normal tissues (P = 0.033). Immunoreactivity for VEGF and MMP-9 was significantly higher in sacral chordoma tissues than in adjacent normal tissues (P = 0.008, P = 0.005). The mean MVD of VEGF and MMP-9 were statistically higher in positive group than in negative group (P = 0.015, P = 0.004), respectively . Moreover, a significant correlation was found between the VEGF and MMP-9 (P = 0.002). The log-rank test revealed that continuous disease-free survival time (CDFS) was significantly shorter in the MMP-9-positive group than in the MMP-9-negative group (P = 0.019), but the difference in the VEGF-positive group and the VEGF-negative group was not statistically significant (P = 0.938). Our data suggest that VEGF and MMP-9 might act with a synergistic effect and can positively regulate the angiogenesis in sacral chordoma. Positive expression of MMP-9 might indicate the local recurrence of sacral chordoma. The result suggests that some specific drugs which inhibit VEGF, MMP-9, or their receptors may have a good therapeutic effect for sacral chordoma.
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页码:357 / 363
页数:6
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共 102 条
[1]  
Samson IR(1993)Operative treatment of sacrococcygeal chordoma. A review of twenty-one cases J Bone Joint Surg Am 75 1476-1484
[2]  
Springfield DS(2002)First histologically confirmed case of a classic chordoma arising in a precursor benign notochordal lesion: differential diagnosis of benign and malignant notochordal lesions Skelet Radiol 31 413-418
[3]  
Suit HD(2000)Prognostic factors in chordoma of the sacrum and mobile spine: a study of 39 patients Cancer 88 2122-2134
[4]  
Mankin HJ(2005)Operative management of sacral chordoma J Bone Joint Surg Am 87 2211-2216
[5]  
Yamaguchi T(2010)Prognostic factors of sacral chordoma after surgical therapy: a study of 36 patients Spinal Cord 48 166-171
[6]  
Yamato M(2002)Expression of growth factors and structural proteins in chordomas: basic fibroblast growth factor, transforming growth factor alpha, and fibronectin are correlated with recurrence Neurosurgery 51 753-760
[7]  
Saotome K(2004)Expression of matrix metalloproteinase (MMP)-1, MMP-2, MMP-9, cathepsin B, and urokinase plasminogen activator in non-skull base chordoma Am J Clin Pathol 122 926-930
[8]  
Bergh P(1997)Immunolocalization of matrix metalloproteinases and tissue inhibitors of metalloproteinases in human chondrosarcomas Gen Diagn Pathol 142 129-137
[9]  
Kindblom LG(2003)Expression of VEGF and MMP-9 in giant cell tumor of bone and other osteolytic lesions Life Sci 73 1427-1436
[10]  
Gunterberg B(2002)Increased pre-therapeutic serum vascular endothelial growth factor in patients with early clinical relapse of osteosarcoma Br J Cancer 86 864-869