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Identification of somatostatin receptor subtypes 1 2A 3 and 5 in neuroendocrine tumours with subtype specific antibodies

机译:用亚型特异性抗体鉴定神经内分泌肿瘤中生长抑素受体亚型1、2A3和5

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摘要

Background and aims: Recently, novel somatostatin receptor (sstr) subtype specific ligand analogues have been developed for medical treatment of neuroendocrine tumours expressing different sstrs (sstr1–5). At present, individual expression patterns of sstr subtypes are based on methods such as in situ hybridisation and polymerase chain reaction at the transcriptional level. Therefore, we generated subtype specific antibodies against sstr1, 2A, 3, and 5 and analysed their presence, cellular localisation, distribution, and expression pattern in 33 gastrinomas, 36 insulinomas, and 35 tumours associated with a carcinoid syndrome by immunohistochemistry at the translational level.Methods: Western blotting experiments were performed in the normal human pancreas used as a reference organ and in tumour tissues; at the cellular level, sstrs were localised by immunohistochemistry in tissue paraffin sections.Results: In western blot analyses, the antibodies identified the respective receptors in their correct molecular range in extracts of the pancreas and neuroendocrine tumours. Using immunohistochemistry and immunofluorescence, the antibodies specifically detected the receptors in islet cells of the normal pancreas. Immunohistochemistry in the tumours revealed that all investigated sstr subtypes were highly expressed in the different tumour types. The frequency and expression pattern of the individual sstr subtypes varied considerably not only between the different tumour types but also in each patient.Conclusions: We conclude that immunohistochemistry with subtype specific antibodies can be used in clinical routine work to analyse sstr expression patterns for each patient before treatment and to facilitate well directed individual medical therapy by administering subtype specific somatostatin analogues.
机译:背景与目的:最近,已开发出新型生长抑素受体(sstr)亚型特异性配体类似物,用于治疗表达不同sstrs(sstr1-5)的神经内分泌肿瘤。目前,sstr亚型的个体表达模式是基于诸如转录水平的原位杂交和聚合酶链反应的方法。因此,我们产生了针对sstr1、2A,3和5的亚型特异性抗体,并在翻译水平上通过免疫组织化学分析了它们在33种胃癌,36种胰岛素瘤和35种与类癌综合征相关的肿瘤中的存在,细胞定位,分布和表达模式方法:在作为参考器官的正常人胰腺和肿瘤组织中进行蛋白质印迹实验。结果:在蛋白质印迹分析中,抗体在胰腺和神经内分泌肿瘤的提取物中以正确的分子范围鉴定了相应的受体。使用免疫组织化学和免疫荧光,抗体特异性检测正常胰腺胰岛细胞中的受体。肿瘤中的免疫组织化学显示,所有研究的sstr亚型在不同的肿瘤类型中均高表达。结论:我们得出结论,具有亚型特异性抗体的免疫组织化学可用于临床常规工作,以分析每位患者的sstr表达模式,得出结论:不仅在不同的肿瘤类型之间,而且在每位患者中,每种sstr亚型的频率和表达模式都存在很大差异。在治疗前,并通过给予亚型特异性生长抑素类似物促进定向良好的个体药物治疗。

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