Department of Pathology, Amsterdam University Medical Center, De Boelelaan, 1117, Amsterdam, The Netherlands.
Department of Clinical Epidemiology and Biostatistics, Amsterdam University Medical Centers, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.
Virchows Arch. 2021 Feb;478(2):293-300. doi: 10.1007/s00428-020-02848-y. Epub 2020 Jun 2.
DLL3 might become a predictive immunohistochemical marker in small cell carcinoma of the lung (SCLC). We investigated the influence of pre-analytical handling of samples on the performance of DLL3 immunohistochemistry (IHC) using DLL3 SP347 ready to use assay (Ventana). DLL3 positive cell lines were subjected to different experimental conditions mimicking the pre-analytical variation in daily clinical practice. Formalin fixation of 24 h led to the most optimal results of DLL3 IHC. Longstanding fixation in Cytolyt, methanol-based fixative for cytology samples, but also decalcification using a mix of formic- and hydrochloracid resulted in decreased DLL3 staining. Postponed staining of blanc slides for 3 months also decreased DLL3 IHC. Postponed fixation of the SCLC cell lines did not influence the performance of DLL3 IHC, although this might be different in the tissues than in the cell lines. In conclusion, different pre-analytical variables decrease the performance of DLL3 IHC. These findings are essential for implementing novel predictive immunohistochemical biomarkers in daily pathology practice.
DLL3 可能成为小细胞肺癌 (SCLC) 的预测性免疫组化标志物。我们使用 DLL3 SP347 即用型检测试剂盒(Ventana)研究了样本前处理对 DLL3 免疫组化 (IHC) 性能的影响。DLL3 阳性细胞系经历了不同的实验条件,模拟了日常临床实践中的样本前处理变化。24 小时福尔马林固定可获得 DLL3 IHC 的最佳结果。Cytolyt 长时间固定(细胞学样本的基于甲醇的固定剂)以及使用甲酸-盐酸混合物脱钙会导致 DLL3 染色减少。空白玻片的延迟染色 3 个月也会降低 DLL3 IHC。SCLC 细胞系的延迟固定不会影响 DLL3 IHC 的性能,尽管这在组织中可能与在细胞系中不同。总之,不同的样本前处理变量会降低 DLL3 IHC 的性能。这些发现对于在日常病理实践中实施新的预测性免疫组化生物标志物至关重要。