Shintaku I P, Said J W
Am J Clin Pathol. 1987 Feb;87(2):161-7. doi: 10.1093/ajcp/87.2.161.
This study describes an improved immunohistochemical method for the sensitive and specific identification of estrogen receptors (ERs) in paraffin sections from formalin-fixed and routinely processed breast carcinoma tissues, using DNase pretreatment to expose nuclear antigenic sites and commercially available immunoreagents (including monoclonal antibody) in kit form. Results were compared with dextran-coated charcoal cytosolic assay (DCC) and with conventional immunohistochemistry on frozen sections. Sensitivity and specificity for determinations on paraffin sections were 88% and 86%, respectively, and statistical analysis showed very good agreement between DCC and paraffin sections (kappa = 0.805). The DNase technic on paraffin sections allows excellent correlation between histologic characteristics and ER status and reduces DCC sampling error resulting from stromal dilution and tumor variability. This method offers a reliable and reproducible alternative when tissue is not suitable or unavailable for DCC or frozen tissue analysis and can be used for retrospective studies on stored tissue blocks.
本研究描述了一种改进的免疫组织化学方法,用于在福尔马林固定并常规处理的乳腺癌组织石蜡切片中灵敏且特异地鉴定雌激素受体(ERs),该方法采用DNA酶预处理以暴露核抗原位点,并使用试剂盒形式的市售免疫试剂(包括单克隆抗体)。将结果与葡聚糖包被活性炭胞质测定法(DCC)以及冰冻切片上的传统免疫组织化学方法进行比较。石蜡切片测定的灵敏度和特异性分别为88%和86%,统计分析表明DCC与石蜡切片之间具有很好的一致性(kappa = 0.805)。石蜡切片上的DNA酶技术使组织学特征与ER状态之间具有良好的相关性,并减少了因间质稀释和肿瘤变异性导致的DCC取样误差。当组织不适合或无法用于DCC或冰冻组织分析时,该方法提供了一种可靠且可重复的替代方法,可用于对储存组织块的回顾性研究。