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首页> 外文期刊>Virchows Archiv >Validation of tissue microarray technology in squamous cell carcinoma of the esophagus
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Validation of tissue microarray technology in squamous cell carcinoma of the esophagus

机译:组织芯片技术在食管鳞状细胞癌中的验证

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Tissue microarray (TMA) technology has been developed to facilitate high-throughput immunohistochemical and in situ hybridization analysis of tissues by inserting small tissue biopsy cores into a single paraffin block. Several studies have revealed novel prognostic biomarkers in esophageal squamous cell carcinoma (ESCC) by means of TMA technology, although this technique has not yet been validated for these tumors. Because representativeness of the donor tissue cores may be a disadvantage compared to full sections, the aim of this study was to assess if TMA technology provides representative immunohistochemical results in ESCC. A TMA was constructed containing triplicate cores of 108 formalin-fixed, paraffin-embedded squamous cell carcinomas of the esophagus. The agreement in the differentiation grade and immunohistochemical staining scores of CK5/6, CK14, E-cadherin, Ki-67, and p53 between TMA cores and a subset of 64 randomly selected donor paraffin blocks was determined using kappa statistics. The concurrence between TMA cores and donor blocks was moderate for Ki-67 (κ = 0.42) and E-cadherin (κ = 0.47), substantial for differentiation grade (κ = 0.65) and CK14 (κ = 0.71), and almost perfect for p53 (κ = 0.86) and CK5/6 (κ = 0.93). TMA technology appears to be a valid method for immunohistochemical analysis of molecular markers in ESCC provided that the staining pattern in the tumor is homogeneous.
机译:通过将小型组织活检核心插入单个石蜡块中,已经开发了组织微阵列(TMA)技术,以促进组织的高通量免疫组织化学和原位杂交分析。几项研究已经通过TMA技术揭示了食管鳞状细胞癌(ESCC)的新型预后生物标志物,尽管该技术尚未针对这些肿瘤进行验证。因为与完整切片相比,供体组织核心的代表性可能是一个缺点,所以本研究的目的是评估TMA技术是否在ESCC中提供了代表性的免疫组织化学结果。构建了一个TMA,其中包含108个福尔马林固定,石蜡包埋的食道鳞状细胞癌的三重核心。使用Kappa统计数据确定了TMA核心与64个随机选择的供体石蜡块的子集之间的CK5 / 6,CK14,E-钙粘着蛋白,Ki-67和p53的分化程度和免疫组化染色评分的一致性。对于Ki-67(κ= 0.42)和E-钙黏着蛋白(κ= 0.47),TMA核心与供体区之间的并发性中等,对于分化等级(κ= 0.65)和CK14(κ= 0.71)相当重要,对于TMA核心和供体区块而言p53(κ= 0.86)和CK5 / 6(κ= 0.93)。如果肿瘤中的染色模式是均匀的,TMA技术似乎是对ESCC中的分子标记进行免疫组织化学分析的有效方法。

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