Ikeda Satoshi
Rinsho Byori. 2015 Jun;63(6):769-73.
Fluorescence in situ hybridization (FISH) has recently become important for pathological diagnosis. However, its practical applications is not widespread because FISH protocol with FFPE specimens is complicated. We report a dual detection method by overlapping FISH with fluorescent immunostaining on FFPE sections. This method is characterized by changing buffers for heat treatment without proteolytic enzyme treatment. Subsequent proteolytic enzyme treatment can be omitted using an antigen activation solution, pH9 (Nichirei Corporation), for heat treatment. After the pretreatment, dual detection was achieved by DNA FISH following RNA FISH and fluorescent immunostaining. This protocol visualized gene abnormalities and protein overexpression on the same sections. Of note, in poorly differentiated tumors containing both normal and tumor cells, the tumor cells were clearly identified on the sections, and FISH signals could be counted in these cells. In addition, HER2 mRNA overexpression and gene amplification were simultaneously detected in HER2-positive gastric cancer. Thus, this method should be widely applicable in clinical settings.
荧光原位杂交(FISH)最近在病理诊断中变得很重要。然而,由于FFPE标本的FISH方案复杂,其实际应用并不广泛。我们报告了一种在FFPE切片上通过将FISH与荧光免疫染色重叠进行双重检测的方法。该方法的特点是在不进行蛋白水解酶处理的情况下改变热处理缓冲液。使用pH9的抗原激活溶液(日冷株式会社)进行热处理,可以省略后续的蛋白水解酶处理。预处理后,通过RNA FISH和荧光免疫染色后的DNA FISH实现双重检测。该方案在同一切片上可视化基因异常和蛋白质过表达。值得注意的是,在含有正常细胞和肿瘤细胞的低分化肿瘤中,肿瘤细胞在切片上被清晰识别,并且可以在这些细胞中计数FISH信号。此外,在HER2阳性胃癌中同时检测到HER2 mRNA过表达和基因扩增。因此,该方法应在临床环境中广泛应用。