Tubbs Raymond R, Swain Eric, Pettay James D, Hicks David G
Departments of Anatomical and Clinical Pathology, The Cleveland Clinic Foundation, The Lerner College of Medicine, Cleveland, OH 44195, USA.
J Mol Histol. 2007 May;38(2):141-50. doi: 10.1007/s10735-006-9076-z. Epub 2007 Jan 9.
Tissue microarrays (TMA) are valuable tools for validating results of array-based comparative genomic hybridization (ACGH) and other translational research applications requiring independent verification of genomic gains and losses by fluorescence in situ hybridization (FISH). However, spatial orientation and accurate manual tracking of the TMA cores is challenging and prone to error. Image analysis combined with core tracking software, implemented via an automated FISH scanning workstation, represents a new approach to FISH and TMA-based validation of novel genomic changes discovered by ACGH in breast and other cancers. Automated large-scale tissue microarray validation FISH studies of genomic gains and losses identified by ACGH for breast cancer are feasible using an automated imaging scanner and tracking/classifying software. Furthermore, by leveraging the bifunctional fluorescent and chromogenic properties of the alkaline phosphatase chromogen fast red K and combining the technology with FISH, correlative and simultaneous phenotype/genotype studies may be enabled.
组织微阵列(TMA)是用于验证基于阵列的比较基因组杂交(ACGH)结果以及其他需要通过荧光原位杂交(FISH)独立验证基因组增减情况的转化研究应用的宝贵工具。然而,TMA芯块的空间定位和准确手动追踪具有挑战性且容易出错。通过自动FISH扫描工作站实现的图像分析与芯块追踪软件相结合,代表了一种基于FISH和TMA对ACGH在乳腺癌及其他癌症中发现的新型基因组变化进行验证的新方法。使用自动成像扫描仪和追踪/分类软件,对ACGH鉴定出的乳腺癌基因组增减进行自动化大规模组织微阵列验证FISH研究是可行的。此外,通过利用碱性磷酸酶显色剂固红K的双功能荧光和显色特性,并将该技术与FISH相结合,可以开展相关的同时性表型/基因型研究。