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血管生成受体激酶插入域受体(KDR)广泛分布于人体组织和肿瘤中,并在磷酸化后重新定位于细胞内。一项免疫组织化学研究。

The angiogenic receptor KDR is widely distributed in human tissues and tumours and relocates intracellularly on phosphorylation. An immunohistochemical study.

作者信息

Stewart M, Turley H, Cook N, Pezzella F, Pillai G, Ogilvie D, Cartlidge S, Paterson D, Copley C, Kendrew J, Barnes C, Harris A L, Gatter K C

机构信息

Cancer Research UK Tumour Pathology Group, Nuffield Department of Clinical Laboratory Sciences, University of Oxford, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

出版信息

Histopathology. 2003 Jul;43(1):33-9. doi: 10.1046/j.1365-2559.2003.01644.x.

Abstract

AIMS

Angiogenesis is an important factor in tumour growth and metastasis. Vascular endothelial growth factor receptor 2 (VEGFR-2) or KDR plays a crucial role in angiogenesis. The aim of this study was to raise and characterize antibodies against phosphorylated KDR which could be used for studies on human tissues to assess KDR activation and novel inhibitors of KDR activation in clinical trials.

METHODS AND RESULTS

Three monoclonal antibodies and one rabbit polyclonal antiserum were produced. The specificity of the antibodies was confirmed by ELISA. One of the mouse antibodies and the rabbit polyclonal antiserum reacted with a 200-kDa band on a Western blot of human umbilical vein endothelial cell (HUVEC) lysates, the molecular weight of KDR. Immunohistochemical staining showed that phosphorylated KDR is present in a wide variety of normal tissues including liver, colon and placenta, and is not restricted to endothelium. It was also present in a number of human tumours including breast carcinomas, colonic carcinomas and non-Hodgkin's lymphomas. The pattern of staining was membranous, cytoplasmic and nuclear.

CONCLUSIONS

This study has shown that phosphorylated KDR is present in a wide variety of tumour and tissue types and is not confined to endothelium.

摘要

目的

血管生成是肿瘤生长和转移的一个重要因素。血管内皮生长因子受体2(VEGFR - 2)或激酶插入域受体(KDR)在血管生成中起关键作用。本研究的目的是制备并鉴定针对磷酸化KDR的抗体,这些抗体可用于人体组织研究,以评估KDR激活情况以及在临床试验中KDR激活的新型抑制剂。

方法与结果

制备了三种单克隆抗体和一种兔多克隆抗血清。通过酶联免疫吸附测定(ELISA)确认了抗体的特异性。其中一种小鼠抗体和兔多克隆抗血清在人脐静脉内皮细胞(HUVEC)裂解物的蛋白质印迹上与一条200 kDa的条带发生反应,该条带为KDR的分子量。免疫组织化学染色显示,磷酸化KDR存在于包括肝脏、结肠和胎盘在内的多种正常组织中,并不局限于内皮细胞。它也存在于一些人类肿瘤中,包括乳腺癌、结肠癌和非霍奇金淋巴瘤。染色模式为膜性、胞质性和核性。

结论

本研究表明,磷酸化KDR存在于多种肿瘤和组织类型中,并不局限于内皮细胞。

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