Tian Erming
Myeloma Institute, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Methods Mol Biol. 2018;1792:55-69. doi: 10.1007/978-1-4939-7865-6_5.
The application of fluorescence in situ hybridization (FISH) technology in diagnosis and molecular classification of cancer-risk has become an essential tool in the proceeding of personalized therapy. In multiple myeloma, the precise FISH detection of numerical and structural genetic aberrations can be carried out on metaphase chromosome spreads, interphase nuclei, and formalin fixed paraffin-embedded (FFPE) tissues. To dissect highly complex cancer genomes, a broad variety of novel DNA probes, which outpace supplies from commercial resources on the market, are also crucial to the advanced translational researches. Here, we provide the protocols for the creation of custom-made DNA probes and for conducting hybridizations on various targeting cells and tissues.
荧光原位杂交(FISH)技术在癌症风险诊断和分子分类中的应用已成为个性化治疗进程中的一项重要工具。在多发性骨髓瘤中,可在中期染色体铺片、间期细胞核以及福尔马林固定石蜡包埋(FFPE)组织上对数值和结构遗传畸变进行精确的FISH检测。为剖析高度复杂的癌症基因组,种类繁多的新型DNA探针对于推进转化研究也至关重要,这些探针的数量超过了市场上商业资源的供应量。在此,我们提供了定制DNA探针以及在各种靶细胞和组织上进行杂交的方案。