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[组织学切片上的荧光原位杂交]

[Fluorescence in situ hybridization on histologic sections].

作者信息

Mrhalová Marcela, Kodet Roman

出版信息

Cesk Patol. 2013 Oct;49(4):114-22.

Abstract

I-FISH (fluorescence in situ hybridization on interphasic nuclei) represents a laboratory method linking morphological investigations (histological sections of formaldehyde fixed and paraffin embedded tissues) with molecular techniques (sequence specificity of nucleic acids bases for a certain locus). I-FISH is relatively undemanding for a laboratory workout, but offering a lot of important information about the investigated cells. Within a scope of pathology departments I-FISH is utilized mostly in diagnostics of neoplasms. I-FISH is helpful in detecting gene copy numbers (amplifications or deletions), and, importantly, in establishing copy numbers of individual chromosomes (polysomies or monosomies), chromosomal breaks and translocations. At present, I-FISH is used not only for diagnosis and estimation of prognosis, but also as a method to qualify a patient for a targeted biological therapy. Because demands on investigation of solid tumors keep raising I-FISH becomes a part of routine investigations. The aim of this paper is to summarize principles and the utility of I-FISH and to help the interested readers in finding a basic orientation in this laboratory method.

摘要

间期细胞核荧光原位杂交(I-FISH)是一种将形态学研究(甲醛固定、石蜡包埋组织的组织学切片)与分子技术(特定基因座核酸碱基的序列特异性)相结合的实验室方法。I-FISH对实验室操作要求相对较低,但能提供大量有关所研究细胞的重要信息。在病理科范围内,I-FISH主要用于肿瘤诊断。I-FISH有助于检测基因拷贝数(扩增或缺失),重要的是,还能确定单个染色体的拷贝数(多体或单体)、染色体断裂和易位。目前,I-FISH不仅用于诊断和预后评估,还作为一种确定患者是否适合靶向生物治疗的方法。由于对实体瘤研究的要求不断提高,I-FISH已成为常规检查的一部分。本文旨在总结I-FISH的原理和应用,帮助感兴趣的读者在这种实验室方法中找到基本方向。

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