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Relationship between PCNA Proliferating Marker and Angiogenesis

机译:PCNA增殖标志物与血管生成的关系

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The goal of the study was to evaluate the prognosis significance of intratumor angiogenesis that was compared with PCNA proliferating marker, histology grade, mitotic index, tumor size, and histology type. The study had been realized using different histology types of bitch mammary tumors according to WHO classifications. There were evaluated some potential angiogenesis markers, such as intratumor microvessel density, total microvascular area and perimeter according to microscopic tumor area, and average vessel area and perimeter in different benign and malign mammary tumors. The study was realized in 8 bitch mammary tumors represented by two benign lesions (simple adenoma and fibroadenoma) and 6 carcinomas (grade I, II and III tumors). From all tumors had been harvested fragments represented by 5 mm slices that were fixed in 10% buffered formalin and proceeded by paraffin technique. The slides were stained by usual methods (HE and TM). To realize immunohistochemistry reaction paraffin embedded slices were attached onto silanized glass slides (Dako). PCNA proliferating marker (clone PC10, izotype IgG2a kappa - Dako) was evaluated by counting by 3 evaluators 8-10 high power magnified fields (400x), about 1000 cells (immunomarked nuclei). There was established average PCNA percentage for each tumor type. Intratumor angiogenesis had been established using CD31 marker (clone JC70A, izotype IgG1 kappa - Dako) and evaluated using semiautomatic image analysis method. Both immunohistochemical reactions utilized LSAB technique.To evaluate new methods necessary to establish bitch mammary tumors malignancy, which is important for mammary cancer prognosis, we utilized several malignancy markers. Also, because intratumor angiogenesis quantification provided contradictory results obtained by many authors, this parameter was related and compared with classic and reliable markers (PCNA antigen, mitotic index, histology grade, tumor size, and tumors characteristics).
机译:该研究的目的是评估与PCNA增殖标志物,组织学等级,有丝分裂指数,肿瘤大小和组织学类型相比的肿瘤内血管生成的预后意义。根据WHO的分类,已使用不同组织学类型的母犬乳腺肿瘤实现了该研究。评价了一些潜在的血管生成标志物,如肿瘤内微血管密度,根据显微肿瘤面积的总微血管面积和周长,以及不同良性和恶性乳腺肿瘤中的平均血管面积和周长。该研究在以两种良性病变(单纯性腺瘤和纤维腺瘤)和6种癌(I,II和III级肿瘤)为代表的8种母乳腺肿瘤中得以实现。从所有肿瘤中收获了以5mm切片表示的片段,将其固定在10%福尔马林缓冲液中,并通过石蜡技术进行处理。用常规方法(HE和TM)对载玻片染色。为了实现免疫组织化学反应,将石蜡包埋的切片附着在硅烷化的载玻片上(Dako)。通过3位评估员在8-10个高倍放大视野(400x)中计数约1000个细胞(免疫标记的细胞核)来评估PCNA增殖标记物(克隆PC10,izotype IgG2a kappa-Dako)。已建立每种肿瘤类型的平均PCNA百分比。使用CD31标记物(克隆JC70A,izotype IgG1 kappa-Dako)建立了肿瘤内血管生成,并使用半自动图像分析方法进行了评估。两种免疫组化反应均使用LSAB技术。为评估建立母犬乳腺肿瘤恶性肿瘤的新方法,这对于乳腺癌的预后至关重要,我们使用了几种恶性肿瘤标志物。另外,由于肿瘤内血管生成的量化提供了许多作者所得出的相互矛盾的结果,因此该参数与经典可靠的标记(PCNA抗原,有丝分裂指数,组织学等级,肿瘤大小和肿瘤特征)相关并进行了比较。

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