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CD147、PCNA、VEGF和MMPs在骨巨细胞瘤中的表达及临床意义 被引量:7

Expression of CD147,PCNA,VEGF and MMPs in giant cell tumor of bones and its clinical significance
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摘要 背景:骨巨细胞瘤(giant cell tumor of bone,GCT)是一种具有低度恶性潜能的肿瘤,目前的主要治疗方法为临床手术治疗,局部侵袭性生长和术后复发率40%~50%,其病理学分级与影像学分型均不能对临床表现进行精确的预测,找到其他影响GCT生物学行为和预后的相关因素并寻找新的治疗途径尤为重要。目的:研究CD147、PCNA、VEGF、MMPs等分子在GCT组织中的表达,探讨其相互关系及与临床病理和预后的关系。方法:运用免疫组织化学S-P法,检测CD147、PCNA、VEGF、MMPs等分子在68例GCT患者中的表达,分析其相互关系以及与肿瘤临床病理资料、Jaffe分级及复发的关系。结果:CD147、MMP-2、MMP-9、VEGF阳性表达与患者年龄、性别等因素无关;CD147、MMP-2阳性表达在Jaffe各级之间有显著性差异(P<0.05),CD147、MMP-2、MMP-9在预后各分组间表达有显著性差异(P<0.05);CD147与MMP-9、VEGF、MVD、PCNA表达呈正相关(r=0.271,P=0.025;r=0.411,P=0.000;r=0.872,P=0.000;r=0.394,P=0.001)。结论:CD147与GCT的恶变、复发有关,并且和MMP-9、VEGF、MVD、PCNA的表达密切相关,可作为评价GCT恶性程度和判断预后的重要指标,并可作为化学治疗的新靶点。 Background: Giant cell tumor of bone (GCT) is a potential malignant tumor, and the main treatment is clinical surgery. Local aggressive growth and postoperative recurrence scale to all as high as 40% - 50%. The pathology classification andimage of GCT cannot precisely predict its clinical behavior, so it's very important to find a new way of treatment and other factors which relate to GCT's biological behavior and prognosis. Objective: To study the expression of CD147, PCNA, VEGF and MMPs in GCT and its relationship to clinical pathology and prognosis.Methods: The expression level of CD147, PCNA, VEGF and MMPs in 68 patients with GCT was detected by S-P immunohiso- chemistry. The relationship between each other, the clinical pathological data, Jaffe classification and recurrence was analyzed. Results : The significant difference of expression level of CD147 and MMPs was found in the cases of GCT with Jaffe grad- ing, prognosis (P 〈 0. 05), but not with the age and gender of the patients. The expression of CD147 was positively corre- lated to MMP-9, VEGF, MVD and PCNA (r =0. 271, P =0. 025; r =0. 411, P =0. 000; r =0. 872, P =0. 000; r = 0.394, P =0. 001).Conclusions: The expression level of CD147 in GCT is correlated with invasion and recurrence, and positively related to MMP-9, VEGF, MVD and PCNA. CD147 may be an important indicator in evaluating the malignant degree and prognosis of GCT, and can be a new target for chemotherapy.
出处 《中国骨与关节外科》 2012年第1期65-71,共7页 Chinese Journal of Bone and Joint Surgery
基金 国家重点基础研究发展计划(973计划 2009CB521703) 国家自然科学基金30300355
关键词 骨巨细胞瘤 细胞外基质金属蛋白酶诱导因子 基质金属蛋白酶 血管内皮生长因子 免疫组织化学 giant cell tumor of bone extracellular matrix metalloproteinases inducer matrix metalloproteinases vascularendothelial growth factor immunohistochemistry
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参考文献29

  • 1Stewart CJ,Crook ML.CD147(EMMPRIN)and matrix metallo-proteinase-2expression in uterine endometrioid adenocarcinoma.Pathol Research Pract,2011,207(1):30-36.
  • 2Zhou Q,Zhu Y,Deng Z,et al.VEGF and EMMPRIN expression correlates with survival of patients with osteosarcoma.Surg Oncol,2011,20(1):13-19.
  • 3赵彤,朱梅刚,黄宗义,张亚历,张素娟,李梅芳.肺癌癌基因蛋白产物同步检测的对比分析[J].癌症,1995,14(1):13-15. 被引量:54
  • 4Wang B,Xu YF,He BS,et al.RNAi-mediated silencing of CD147inhibits tumor cell proliferation,invasion and increases chem-osensitivity to cisplatin in SGC7901cells in vitro.J Exp Clin Cancer Res,2010,29:61.
  • 5Yurchenko V,Constant S,Eisenmesser E,et al.Cyclophilin CD147interactions:a new target for anti-inflammatory therapeutics.Clin Exp Immunol,2010,160(3):305-317.
  • 6Kanekura T,Chen X,Kanzaki T.Basigin(CD147)is expressed on melanoma cells and induces tumor cell invasion by stimulating pro-duction of matrix metalloproteinases by fibroblasts.Int J Cancer,2002,99(4):520-528.
  • 7Igakura T,Kadomatsu K,Taguchi O,et al.Roles of basigin,a member of the immunoglobulin superfamily,in behavior as to an irri-tating odor,Iymphocyte response,and blood-brain barrier.Bio-chem Biophys Res Commun,1996,224(1):33-36.
  • 8Saxena DK,Oh-Oka T,Kadomatsu K,et al.Behaviour of a spermsurface transmembrane glycoprotein basigin during epididymal matura-tion and its role in fertilization in mice.Reproduction,2002,123(3):435-444.
  • 9Naruhashi K,Kadomatsu K,Igakura T,et a1.Abnormalties of sensory and memory functions in mice lacking Bsggene.Biochem Biophys Res Commun,1997,236(3):733-737.
  • 10Westerlund A,Hujanen E,Puistola U,et al.Fibroblasts stimu-late human ovarian cancer cell invasion and expression of72-kDa ge-latinase A(MMP-2).Gynecol Oncol,1997,67(1):76-82.

二级参考文献14

  • 1Guo H, Majmudar G, Jensen TC, et al. Characterization of the gene for human EMMPRIN, a tumor cell surface inducer of matrix metalloproteinases. Gene, 1998, 220: 99-108.
  • 2Sameshima T, Nabeshima K, Toole BP, et al. Expression of EMMPRIN (CD147), a cell surface inducer of matrix metalloproteinases, in normal human brain and gliomas. Int J Cancer, 2000,88:21-27.
  • 3Biswas C, Zhang Y, Decastro R, et al. The Human tumor cell-derived collagenase stimulatory factor (renamed EMMPRIN) is a member of the immunoglobulin superfamily. Cancer Res, 1995, 55: 434-439.
  • 4Guo H, Li R, Zucker S, et al. EMMPRIN(CD147), an inducer of matrix metalloproteinase synthesis, also binds interstitial collagenase to the tumor cell surface. Cancer Res, 2000, 60:888-891.
  • 5Gilles C, Polette M, Piette J, et al. High level of MT-MMP expression is associated with invasiveness of cervical cancer cells. Int J Cancer,1996, 65:209-221.
  • 6Jiang JL, Zhou Q, Yu MK, et al. The involvement of HAb18G/CD147 in regulation of store-operated calcium entry and metastasis of human hepatoma cells. J Biol Chem. 2001, 276: 46870-46877.
  • 7Kimura N, Kurokawa K, Yamamoto K, et al. Molecular identification of the antigens recognized by monoclonal antibody JT95 specific for thyroid carcinomas. Biochem Biophys Res Commun, 1998, 251: 449-453.
  • 8Fernandez HA, Kallenbach K, Seghezzi G, et al. Inhibition of endothelial cell migration by gene transfer of tissue inhibitor of metalloproteinases-1. J Surg Res, 1999, 82:156-162.
  • 9Bae DG, Gho YS, Yoon WH, et al. Arginine-rich anti-vascular endothelial growth factor peptides inhibit tumor growth and metastasis by blocking angiogenesis. J Biol Chem, 2000, 275 : 13588-13596.
  • 10Guo Y, Higazi AA, Arakelian A, et al. A peptide derived from the nonreceptor binding region of urokinase plasminogen activator (uPA) inhibits tumor progression and angiogenesis and induces tumor cell death in vivo. FASEB J, 2000, 14: 1400-1410.

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