肿瘤标志物在人胃肠道血液和淋巴管中的表达

K. Ayensu, T. Madgwick
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引用次数: 0

摘要

肿瘤的行为不能有效地评估组织学组织切片,因此,特定的生物标志物被用来预测肿瘤的行为。同时,生物标志物必须提供预后信息,对患者的治疗是必要的。通过从结肠和il-eum连续切割肿瘤组织切片,有效地评估了抗内毒素CD105和CD34抗体的免疫染色。结果与正常组织切片的数据相关联,证实了抗cd105抗体在评估肿瘤血管生成方面优于其他泛内皮细胞标志物,如抗cd34。此外,使用针对内皮细胞的CD105和CD34抗体评估微血管密度,以定量区分肿瘤新生血管和任何预先存在的血管。因此,我们评估了由增殖、迁移和来自原有血管的终分化内皮细胞的重塑引起的肿瘤血管生成,提供了一种有用的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tumour marker expression in blood and lymphatic vessels of human gastrointestinal tract
The behaviour of tumours cannot be effectively assessed on histological tissue sections only, hence, specific bi-ological markers were used to predict tumour behaviour. The biological markers at the same time must provide prognostic information, necessary for the treatment of patients. The immunostaining of antibodies against endo-glins CD105 and CD34 were effectively assessed using serially cut tumour tissue sections from the colon and il-eum. The results were correlated with data from normal tissue sections, and confirmed the superiority of anti-CD 105 antibody over other pan-endothelial cell markers, such as anti-CD34 in the assessment of tumour angio-genesis. In addition, micro vessel density was assessed using CD105 and CD34 antibodies directed towards en-dothelial cells to distinguish quantitatively tumour neovascularisation and any pre-existing blood vessels. Hen-ce, tumour angiogenesis arising from proliferation, migration, and remodelling of terminally differentiated en-dothelial cells from pre-existing blood vessels were assessed, providing a useful means of approaching therapy.
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