Kiprianova Irina, Just Alexandra, Leuchs Barbara, Rommelaere Jean, Angelova Assia L
Division of Tumor Virology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
BIORON GmbH, Ludwigshafen, Germany.
Methods Mol Biol. 2020;2058:295-306. doi: 10.1007/978-1-4939-9794-7_20.
Fluorescence in situ hybridization (FISH) is a specific, sensitive, accurate, and reliable technique widely applied in both research and clinic. Here we describe the detailed protocol of a FISH method established by us to serve the scientific purposes of the first oncolytic parvovirus clinical trial (ParvOryx01). This trial was launched in Germany in 2011. After trial completion in 2015, results were published in Molecular Therapy in 2017. The primary purpose of the trial was to evaluate the safety of an oncolytic parvovirus, H-1PV (ParvOryx), in recurrent glioblastoma patients. In addition, the efficiency of H-1PV tumor targeting after intratumoral or systemic virus administration was assessed by FISH detection of viral nucleic acids (genomic single-stranded DNA, mRNA and parvovirus double-stranded replicative forms) in formalin-fixed paraffin-embedded glioblastoma tissues resected at day 10 after ParvOryx treatment. The FISH method allowed the detection-for the first time in humans-of H-1PV replication markers in brain tumors of parvovirus-treated patients. A protocol combining mRNA FISH with simultaneous immunofluorescent staining for tumor and tumor microenvironment markers was also developed and is described here, in order to better characterize H-1PV cellular targets and H-1PV treatment-associated tumor microenvironment changes.
荧光原位杂交(FISH)是一种特异性强、灵敏度高、准确且可靠的技术,广泛应用于科研和临床领域。在此,我们描述一种由我们建立的FISH方法的详细方案,以服务于首个溶瘤细小病毒临床试验(ParvOryx01)的科学目的。该试验于2011年在德国启动。2015年试验完成后,结果于2017年发表在《分子治疗》杂志上。该试验的主要目的是评估溶瘤细小病毒H-1PV(ParvOryx)在复发性胶质母细胞瘤患者中的安全性。此外,通过对ParvOryx治疗后第10天切除的福尔马林固定石蜡包埋胶质母细胞瘤组织中的病毒核酸(基因组单链DNA、mRNA和细小病毒双链复制形式)进行FISH检测,评估瘤内或全身给予病毒后H-1PV靶向肿瘤的效率。FISH方法首次在人类中检测到细小病毒治疗患者脑肿瘤中的H-1PV复制标志物。还开发了一种将mRNA FISH与肿瘤和肿瘤微环境标志物的同步免疫荧光染色相结合的方案,并在此进行描述,以便更好地表征H-1PV细胞靶点和H-1PV治疗相关的肿瘤微环境变化。