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人脑胶质瘤组织中趋化因子受体和血管内皮细胞生长因子的表达 被引量:3

Expression of CXCR7 and VEGF in Gliomas of Human
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摘要 目的:探讨趋化因子受体(CXCR7)和血管内皮细胞生长因子(VEGF)在胶质瘤患者肿瘤组织的表达及其与胶质瘤发生发展的关系。方法:应用组织芯片技术及免疫组织化学SP法,检测10例正常脑组织和69例胶质瘤组织CXCR7和VEGF的表达水平,比较不同病理分级胶质瘤组织中CXCR7和VEGF的表达水平,采用Spearman法分析胶质瘤组织中CXCR7和VEGF的相关性。结果:正常脑组织(对照组)、低级别胶质瘤组及高级别胶质瘤组患者脑组织中CXCR7、VEGF的表达阳性率逐渐升高,组间比较差异有统计学意义(P <0. 05);CXCR7、VEGF表达随胶质瘤恶性程度的增加表达逐渐上调,呈正相关(r=0. 327,P <0. 01); Spearman等级分析显示,CXCR7与VEGF在69例胶质瘤组织中的表达呈正相关关系(r=0. 327,P <0. 01)。结论:CXCR7及VEGF在胶质瘤组织中表达上调,且随着肿瘤恶性程度的增高而增强,CXCR7和VEGF在胶质瘤的发生、发展过程中可能起协同作用。 Objective:To investigate the expression of CXCR7 and VEGF in tissue of gliomas,and the relationship between CXCR7,VEGF and pathologic grading as well as tumorigenesis of gliomas. Methods: Immunohistochemistry (SP) tissue chip were applied to evaluate the expression of CXCR7 and VEGF in 10 cases of normal controls and 69 cases of human gliomas; comparing expression of CXCR7 and VEGF in different pathological gradings of gliomas; adopting Spearman assay to analyze relevance of CXCR7 and VEGF in gliomas tissue. Results: The positive expression rates of CXCR7 and VEGF gradually increased in healthy brain tissue of control group, low grade gliomas group and high grade gliomas group, comparison between groups was statistical significant ( P 〈0.05). The expression of CXCR7 and VEGF upregulated with the increase of malignant level of gliomas, which was positively correlated ( r=0.327,P〈 0.01). Spearman grading analysis indicated that expression of CXCR7 and VEGF was positively correlated in 69 cases of gliomas tissue ( r=0.327,P〈 0.01). Conclusion: The expression of CXCR7 and VEGF in gliomas was upregulated and the positive reaction rate of CXCR7 and VEGF were increased with the increase of tumor malignancy. The results indicate CXCR7 and VEGF may play a co-ordinating role in the tumorigenesis of gliomas.
作者 田陈 吴芳 于海云 郭郑旻 李宁 李红梅 TIAN Chen;WU Fang;YU Haiyun;GUO Zhengmin;LI Ning;LI Hongmei(Department of Pathology,Capital Medical University Dianli Hospital,Beijing 100073,China;Teaching Division of Biochemistry and Molecular Biology,School of Basic Medicine,Guizhou Medical University,Guiyang 550025,Guizhou,China)
出处 《贵州医科大学学报》 CAS 2018年第9期1046-1049,1064,共5页 Journal of Guizhou Medical University
基金 贵州省科学技术基金项目[黔科合LH字(2014)7084]
关键词 胶质母细胞瘤 趋化因子受体 血管内皮细胞生长因子 免疫组织化学 芯片分析技术 基因表达 gliomas chemokine receptor vascular endothelial growth factor immunohistochemistry microchip analytical procedures gene expression
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  • 1杨小立,王茂德,刘守勋,王拓,王鸿雁.人脑胶质瘤基质金属蛋白酶-9的表达与肿瘤血管形成的相关性及对其肿瘤防治的意义[J].中国临床康复,2004,8(23):4779-4781. 被引量:5
  • 2Wai P Y,Kuo P C.The role of osteopontin in tumor metastasis[J].J of Surg Res,2004,121(2):228-241.
  • 3Takano S,Tsuboi K,Tomono Y,et al.Tissue factor,osteopontin.alphavbeta3 integrin expression in microvasculature of gliomas associated with vascular endothelial growth factor expression[J].Br J Cancer,2000,82(12):1967-1973.
  • 4Kim M S,Park M J.Moon E J.et al.Hyaluronic acid induces osteopontin via the phosphatidylinositol 3-kinase/Akt pathway to enhance the motility of human glioma cells[J].Cancer Res,2005,65(3):686-691.
  • 5Jang T.Osteopontin expression in intratumoral astrocytes marks tumor progression in glioma as induced by prenatal exposure to N-ethyl-N-nitrosourea[J].Am J Pathol,2006,168(5):1676-1685.
  • 6Kzchra,Beaulieu E,Delbecchi L,et al.Expression of matrix metallo proteinases and their inhibitors in human brain tumors[J].clin Exp Metastasis,1999,17(7):555-66.
  • 7Pei D,Weiss S.Trans memebrane-deletion metants of the membranetype matrix metalloproteinase -1 process progelatinase and express intrinsic matrix-degrading activity[J],J Biol Chem,1996,27(15):9135-9140.
  • 8Rangaswami H,Bulbule A,Kundu G C.Nudear factor inducing kinase plays crucial role in osteopontin induced MAPK/IKK dependent nuclear factor RB-mediated promatrix metalloproteinase-9 activation[J].J Biol Chem,2004,279(37):38921-38935.
  • 9江常震,林志雄,陈振斌,陈锦峰,何理盛.MMP-2和MMP-9对人脑胶质瘤侵袭微生态系统中血瘤屏障的影响[J].中国神经免疫学和神经病学杂志,2003,10(1):48-50. 被引量:8
  • 10孙现军,姜希宏,侯文红,马恒.骨桥蛋白与MMP-9在胃癌中的表达及其与临床病理特征的关系[J].肿瘤防治杂志,2003,10(4):370-372. 被引量:15

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