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VEGF及其受体KDR在垂体腺瘤中的表达与肿瘤血管形成的关系[J]. 肿瘤防治研究, 2005, 32(01): 8-10. DOI: 10.3971/j.issn.1000-8578.2461
引用本文: VEGF及其受体KDR在垂体腺瘤中的表达与肿瘤血管形成的关系[J]. 肿瘤防治研究, 2005, 32(01): 8-10. DOI: 10.3971/j.issn.1000-8578.2461
Correlation between the Expression of Vascular Endothel ial Growth Factor and Its Receptor KD R and Angiogenesis in Human Pituitary Adenomas[J]. Cancer Research on Prevention and Treatment, 2005, 32(01): 8-10. DOI: 10.3971/j.issn.1000-8578.2461
Citation: Correlation between the Expression of Vascular Endothel ial Growth Factor and Its Receptor KD R and Angiogenesis in Human Pituitary Adenomas[J]. Cancer Research on Prevention and Treatment, 2005, 32(01): 8-10. DOI: 10.3971/j.issn.1000-8578.2461

VEGF及其受体KDR在垂体腺瘤中的表达与肿瘤血管形成的关系

Correlation between the Expression of Vascular Endothel ial Growth Factor and Its Receptor KD R and Angiogenesis in Human Pituitary Adenomas

  • 摘要: 目的 探讨血管内皮生长因子(VEGF) 及其受体( KDR) 的表达与垂体腺瘤血管生成的关系。方法 应用免疫组织化学S2P 法检测58 例人垂体腺瘤中的V E GF 及KD R 的表达,并对血管进行染色、计数。结果 其中54 例有VEGF 的表达(占93. 1 %), 阳性表达主要位于肿瘤细胞胞膜及胞浆; KD R 在47 例中有阳性表达(占81. 0 %), 阳性表达位于肿瘤血管内皮细胞、肿瘤细胞胞膜及胞浆。VEGF 和KD R 表达与垂体腺瘤的侵袭性密切相关;V E GF 和KD R 高表达组微血管密度明显高于低表达组( P <0. 01) 。结论 VEGF 以旁分泌、自分泌形式协同KDR 促进垂体腺瘤血管的生成,并与垂体腺瘤的侵袭密切相关。

     

    Abstract: Objective  To investigate the correlation between the expression of vascular endothelial growth factor (V E GF) and it s receptor KD R and angiogenesis in human pituitary adenomas. Methods  V E GF and KD R were detected in 58 cases pituitary adenomas by immunohistochemical S-P technique. Microvessel density was determined by immunostaining for factor CD34 related antigen. Results  VEGF was expressed in 54 cases (93. 1 %), mainly located at cytoplasm or the membrance of pituitary adenomas cells ;KD R was expressed in 47 cases (81. 0 %), it was located in the vascular endothelial cell of pituitary adenomas tissues and in the cytoplasm or the membrane of the pituitary adenomas cell. Both VEGF expression and KD R were well correlated with the invasiveness. The microvascular density (MVD) was significantly greater in VEGF and KD R higher expression groups than in lower group s ( P < 0. 01) . Conclusion V E GF promotes angiogenesis synergism KDR by paracrining or autocining in pituitary adenomas, and take part in tumor invasiveness.

     

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