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VEGF、KDR在卵巢上皮性肿瘤组织中的表达及其与血管新生的关系 被引量:1

Expression of VEGF and KDR in epithelial ovarian tumor tissue and its relationship with microvascular density
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摘要 目的:探讨VEGF、KDR在卵巢上皮性肿瘤组织中的表达及其与微血管密度的关系。方法:用免疫组化技术检测卵巢上皮性肿瘤组织中VEGF、KDR的表达并测定IOD值,在光镜下计数MVD。结果:VEGF和KDR的表达在卵巢良恶性肿瘤组织中有显著性差异。VEGF表达阳性的MVD值显著高于VEGF表达阴性者(P<0.01);MVD与VEGF、KDR表达呈正相关(〈P0.05),VEGF表达与KDR表达呈正相关(P〈0.01)结论:VEGF、KDR和MVD均能反映卵巢上皮性肿瘤的良恶性和恶性进展程度,可作为衡量卵巢肿瘤良恶性及判断预后的重要参考指标。 Objective:To study the expression of VEGF and its receptor KDR in epithelial ovarian tumor tissue and the relationship between them and MVD). Methods: Expression of VEGF. KDR and were examined by immunohistochemical technique in epithelial ovarian tumor tissue. The integral optical density (IOD) was measured. MVD was counted by light microscope. Results:The positive rate and IOD of VEGF and KDR expression were increased in sequence of the comparion cases, benign cases and malignant cases,and there were significant differences among them( P 〈 0.01 ); The average MVD was higher in the malignant cases with positive expression of VEGF than those without expression of VEGF ( P 〈 0.01 ); MVD was significantly correlated with the expression of VEGF and KDR( P 〈 0.05 ). The expression of VEGF was significantly correlated with the expression of KDR. ( P 〈 0.01 ). Conclusion:Quantification of VEGF, KDR and MVD in epithelial ovarian tumor may provide valuable markers for estimating the prognosis of the ovarian epithelial tumors.
作者 曹宁川 杨娜
出处 《求医问药(下半月刊)》 2012年第4期22-23,共2页 Seek Medical and Ask The Medicine
关键词 卵巢上皮性肿瘤 VEGF KDR 血管新生 MVD Epithelial ovarian tumor VEGF KDR angiogenesis MVD
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  • 1Dvorak HF. Vascular permeability factor/vascular endothelial growth factor:A critical cytokine in tumor angiogenesis and a potential target for diagnosis and therapy[J].Journal of Clinical Oncology,2002,(21):4368-4380.doi:10.1200/JCO.2002.10.088.
  • 2Zeng H,Dvorak HF,Mukhopdhyay D. Vascular permeability factor (VPF)/vascular endothelial growth factor (VEGF) receptorI down-modulates VPF/VEGF receptor-2-mediated endothelial cell proliferation,but not migration,through phosphatedylinositol 3-kinase-dependent pathways[J].Journal of Biological Chemistry,2001,(29):26969-26979.doi:10.1111/j.1365-2133.2009.09287.x.
  • 3Ogawa S,Oku A,Sawano A. A novel type of vascular endothelial growth factor,VEGF-E (NZ-7 VEGF),preferentially utilizes KDR/FIk-1 receptor and carries a potent mitotic activity without heparin-binding domain[J].Journal of Biological Chemistry,1998,(47):31273-31282.doi:10.1074/jbc.273.47.31273.

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