Optimization of Fluorescence In Situ Hybridization Protocols in the Era of Precision Medicine

Sarah Kudman, Alissa Semaan, Majd Al Assaad, Swarna Gogineni, M. Laura Martin, Susan Mathew, Olivier Elemento, David C. Wilkes, Juan Miguel Mosquera
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Abstract

Fluorescence in situ hybridization (FISH) is a cytogenetic assay that is widely used in both clinical and research settings to validate genetic aberrations. Simple in principle, it is based on denaturation and hybridization of a DNA probe and its complementary sequence; however, it is subject to continuous optimization. Here we share how in-house FISH can be optimized using different control tissues to visualize and ultimately validate common and novel genetic abnormalities unearthed by next-generation sequencing (NGS). Seven specific FISH probes were designed and labeled, and conditions for eight tissue types and one patient-derived tumor organoid were optimized. Formalin-fixed paraffin-embedded (FFPE) tissue slides were used for each experiment. Slides were first deparaffinized, then placed in a pretreatment solution followed by a digestion step. In-house FISH probes were then added to the tissue to be denatured and hybridized, and then washed twice. To obtain optimal results, probe concentration, pepsin incubation time, denaturation, and the two post-hybridization washes were optimized for each sample. By modifying the above conditions, all FISH experiments were optimized in separate tissue types to investigate specific genomic alterations in tumors arising in those tissues. Signals were clear and distinct, allowing for visualization of the selected probes. Following this protocol, our lab has quickly optimized 11 directly labeled in-house FISH probes to support genetic aberrations nominated by NGS, including most recent discoveries through whole-genome sequencing analyses. We describe a robust approach of how to advance in-house labeled FISH probes. By following these guidelines, reliable and reproducible FISH results can be obtained to interrogate FFPE slides from benign, tumor tissues, and patient-derived tumor organoid specimens. This is of most relevance in the era of NGS and precision oncology. © 2024 Wiley Periodicals LLC.

Basic Protocol 1: Metaphase FISH optimization

Support Protocol 1: In-house probe labeling and preparation

Support Protocol 2: Metaphase spread preparation

Basic Protocol 2: Optimization of FISH on formalin-fixed paraffin-embedded tissue

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在精准医学时代优化荧光原位杂交方案。
荧光原位杂交(FISH)是一种细胞遗传学检测方法,广泛应用于临床和研究领域,用于验证基因畸变。其原理简单,基于 DNA 探针及其互补序列的变性和杂交,但需要不断优化。在此,我们将分享如何利用不同的对照组织对内部 FISH 进行优化,以显示并最终验证下一代测序(NGS)发现的常见和新型基因异常。我们设计并标记了七种特异性 FISH 探针,并优化了八种组织类型和一种源自患者的肿瘤类器官的条件。每次实验都使用福尔马林固定石蜡包埋(FFPE)组织切片。首先对切片进行脱石蜡处理,然后将其放入预处理溶液中进行消化。然后将自制的 FISH 探针加入待变性和杂交的组织中,再清洗两次。为了获得最佳结果,对每个样本的探针浓度、胃蛋白酶孵育时间、变性和杂交后的两次洗涤都进行了优化。通过修改上述条件,对不同组织类型的所有 FISH 实验进行了优化,以研究这些组织中肿瘤的特定基因组变化。信号清晰明确,使所选探针可视化。按照这一方案,我们实验室迅速优化了 11 种直接标记的内部 FISH 探针,以支持 NGS 发现的基因畸变,包括最近通过全基因组测序分析发现的基因畸变。我们介绍了如何推进内部标记 FISH 探针的稳健方法。遵循这些指南,就能获得可靠、可重复的 FISH 结果,对良性肿瘤、肿瘤组织和患者肿瘤类器官标本的 FFPE 切片进行检测。这在 NGS 和精准肿瘤学时代最具现实意义。© 2024 Wiley Periodicals LLC.基本方案 1:分裂期 FISH 优化 支持方案 1:内部探针标记和制备 支持方案 2:分裂期涂片制备 基本方案 2:福尔马林固定石蜡包埋组织的 FISH 优化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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