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4FISH-IF,一种四色双基因 FISH 联合 p63 免疫荧光,用于评估前列腺癌中 NKX3.1 和 MYC 的状态。

4FISH-IF, a four-color dual-gene FISH combined with p63 immunofluorescence to evaluate NKX3.1 and MYC status in prostate cancer.

机构信息

Department of Laboratory Medicine and Pathology/Applied Molecular Oncology, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada.

出版信息

J Histochem Cytochem. 2013 Jul;61(7):500-9. doi: 10.1369/0022155413490946. Epub 2013 May 2.

Abstract

NKX3.1 allelic loss and MYC amplification are common events during prostate cancer progression and have been recognized as potential prognostic factors in prostate cancer after radical prostatectomy or precision radiotherapy. We have developed a 4FISH-IF assay (a dual-gene fluorescence in situ hybridization combined with immunofluorescence) to measure both NKX3.1 and MYC status on the same slide. The 4FISH-IF assay contains four probes complementary to chromosome 8 centromere, 8p telomere, 8p21, and 8q24, as well as an antibody targeting the basal cell marker p63 visualized by immunofluorescence. The major advantages of the 4FISH-IF include the distinction between benign and malignant glands directly on the 4FISH-IF slide and the control of truncation artifact. Importantly, this specialized and innovative combined multiprobe and immunofluorescence technique can be performed on diagnostic biopsy specimens, increasing its clinical relevance. Moreover, the assay can be easily performed in a standard clinical molecular pathology laboratory. Globally, the use of 4FISH-IF decreases analytic time, increases confidence in obtained results, and maintains the tissue morphology of the diagnostic specimen.

摘要

NKX3.1 等位基因丢失和 MYC 扩增是前列腺癌进展过程中的常见事件,已被认为是根治性前列腺切除术或精准放疗后前列腺癌的潜在预后因素。我们开发了一种 4FISH-IF 检测法(双基因荧光原位杂交结合免疫荧光),可在同一张载玻片上同时测量 NKX3.1 和 MYC 状态。该 4FISH-IF 检测法包含四个与 8 号染色体着丝粒、8p 端粒、8p21 和 8q24 互补的探针,以及通过免疫荧光可视化的基底细胞标志物 p63 的抗体。该 4FISH-IF 检测法的主要优点包括直接在 4FISH-IF 载玻片上区分良性和恶性腺体,以及控制截断伪影。重要的是,这种专门的创新联合多探针和免疫荧光技术可以在诊断性活检标本上进行,增加了其临床相关性。此外,该检测法可以在标准的临床分子病理学实验室中轻松进行。总的来说,使用 4FISH-IF 减少了分析时间,提高了对结果的信心,并保持了诊断标本的组织形态。

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