Suppr超能文献

存档细针穿刺细胞学(FNAC)样本:临床分子谱分析的未开发资源。

Archival fine-needle aspiration cytopathology (FNAC) samples: untapped resource for clinical molecular profiling.

机构信息

Genetics Branch, Center for Cancer Research, National Cancer Institute, Bethesda, Bethesda, MD 20892-4265, USA.

出版信息

J Mol Diagn. 2010 Nov;12(6):739-45. doi: 10.2353/jmoldx.2010.090238.

Abstract

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.

摘要

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。

相似文献

引用本文的文献

3
Molecular testing on serous effusion: An update.浆液性积液的分子检测:最新进展
Cytojournal. 2021 Dec 6;18:35. doi: 10.25259/Cytojournal_55_2020. eCollection 2021.
5
Next generation sequencing in cytology.细胞学中的下一代测序。
Cytopathology. 2021 Sep;32(5):588-595. doi: 10.1111/cyt.12974. Epub 2021 Apr 1.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验