Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Bethesda, MD 20892-4265, USA.
J Mol Diagn. 2010 Nov;12(6):739-45. doi: 10.2353/jmoldx.2010.090238.
Microarray technologies provide high-resolution maps of chromosome imbalances and epigenomic aberrations in the cancer cell genome. Such assays are often sensitive to sample DNA integrity, voiding the utility of many archival pathology specimens and necessitating the special handling of prospective clinical specimens. We have identified the remarkable preservation of higher-molecular weight DNA in archival fine-needle aspiration cytopathology specimens from patients greater than 10 years of age. We further demonstrate the outstanding technical performance of 57 fine-needle aspiration cytopathology samples for aberration detection on high-resolution comparative genomic hybridization array, DNA methylation, and single nucleotide polymorphism genotyping platforms. Forty-four of 46 malignant aspirates in this study manifested unequivocal genomic aberrations. Importantly, matched Papanicolaou and Diff-Quik fine-needle aspiration cytopathology samples showed critical differences in DNA preservation and DNA integrity. Overall, this study identifies a largely untapped reserve of human pathology specimens for molecular profiling studies, with ramifications for the prospective collection of clinical biospecimens.
微阵列技术提供了癌症细胞基因组中染色体失衡和表观基因组异常的高分辨率图谱。此类检测通常对样本 DNA 完整性敏感,排除了许多存档病理学标本的实用性,并需要对前瞻性临床标本进行特殊处理。我们已经确定,在年龄大于 10 岁的患者的存档细针穿刺细胞学标本中,高分子量 DNA 得到了显著保存。我们进一步证明了 57 个细针穿刺细胞学标本在高分辨率比较基因组杂交阵列、DNA 甲基化和单核苷酸多态性基因分型平台上进行异常检测的出色技术性能。在这项研究中,46 个恶性抽吸物中有 44 个表现出明确的基因组异常。重要的是,配对的巴氏涂片和 Diff-Quik 细针穿刺细胞学标本在 DNA 保存和 DNA 完整性方面显示出关键差异。总的来说,这项研究确定了大量未被开发的人类病理学标本用于分子分析研究,这对前瞻性收集临床生物标本具有重要意义。