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血管内皮生长因子受体(FLT-1、KDR、NRP-1)和血小板反应蛋白-1的表达增加与恶性黑色素瘤中的肾小球样微血管增殖相关,这是一种侵袭性血管生成表型。

Increased expression of VEGF-receptors (FLT-1, KDR, NRP-1) and thrombospondin-1 is associated with glomeruloid microvascular proliferation, an aggressive angiogenic phenotype, in malignant melanoma.

作者信息

Straume Oddbjørn, Akslen Lars A

机构信息

Department of Pathology, The Gade Institute, Haukeland University Hospital, Bergen, Norway.

出版信息

Angiogenesis. 2003;6(4):295-301. doi: 10.1023/B:AGEN.0000029408.08638.aa.

Abstract

Glomeruloid microvascular proliferations (GMPs), which are focal proliferative buddings of endothelial cells resembling a renal glomerulus, can be induced experimentally by adenoviral transfer of VEGF-A(165). We recently found that GMPs were present in 13-23% of various human tumours (melanoma, breast-, endometrial- and prostate cancer), and this vascular signature was significantly associated with an impaired prognosis. In the present study, a series of 202 vertical growth phase melanomas were examined for the expression of various angiogenic factors and their receptors. Presence of GMP was associated with increased expression in tumour endothelium of the VEGF-A receptors KDR, FLT-1 and neuropilin-1, as well as VEGF-D protein. Thrombospondin-1 staining in the tumour stroma showed the same relationship. Endothelial cell expression of VEGF-A was increased in GMP endothelium when compared with other intra-tumoural vessels. In contrast, GMP expression of bFGF was decreased. Our findings suggest an important role of VEGF-A and its receptors in GMP formation in human cutaneous melanoma.

摘要

肾小球样微血管增殖(GMPs)是内皮细胞的局灶性增殖芽,类似于肾小体,可通过腺病毒介导的VEGF-A(165)转移实验诱导产生。我们最近发现,在各种人类肿瘤(黑色素瘤、乳腺癌、子宫内膜癌和前列腺癌)中,13%-23%存在GMPs,并且这种血管特征与预后不良显著相关。在本研究中,对一系列202例垂直生长期黑色素瘤进行了各种血管生成因子及其受体表达的检测。GMP的存在与肿瘤内皮中VEGF-A受体KDR、FLT-1和神经纤毛蛋白-1以及VEGF-D蛋白的表达增加有关。肿瘤基质中的血小板反应蛋白-1染色显示出相同的关系。与其他肿瘤内血管相比,GMP内皮中VEGF-A的内皮细胞表达增加。相反,bFGF的GMP表达降低。我们的研究结果表明,VEGF-A及其受体在人类皮肤黑色素瘤的GMP形成中起重要作用。

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